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Literature summary extracted from

  • Campos, N.; Arro, M.; Ferrer, A.; Boronat, A.
    Determination of 3-hydroxy-3-methylglutaryl CoA reductase activity in plants (2014), Methods Mol. Biol., 1153, 21-40.
    View publication on PubMed

Activating Compound

EC Number Activating Compound Comment Organism Structure
1.1.1.34 DTT
-
Vigna radiata var. radiata
1.1.1.34 DTT
-
Hordeum vulgare
1.1.1.34 DTT
-
Spinacia oleracea
1.1.1.34 DTT
-
Pisum sativum
1.1.1.34 DTT
-
Zea mays
1.1.1.34 DTT
-
Solanum tuberosum
1.1.1.34 DTT
-
Nicotiana tabacum
1.1.1.34 DTT
-
Glycine max
1.1.1.34 DTT
-
Lithospermum erythrorhizon
1.1.1.34 DTT
-
Arabidopsis thaliana
1.1.1.34 DTT
-
Picea abies
1.1.1.34 DTT
-
Brassica napus
1.1.1.34 DTT
-
Arachis hypogaea
1.1.1.34 DTT
-
Medicago sativa
1.1.1.34 DTT
-
Daucus carota
1.1.1.34 DTT
-
Solanum lycopersicum
1.1.1.34 DTT
-
Helianthus tuberosus
1.1.1.34 DTT
-
Raphanus sativus
1.1.1.34 DTT
-
Gossypium hirsutum
1.1.1.34 DTT
-
Ochromonas malhamensis
1.1.1.34 DTT
-
Hevea brasiliensis
1.1.1.34 DTT
-
Persea americana
1.1.1.34 DTT
-
Cucumis melo
1.1.1.34 DTT
-
Cannabis sativa
1.1.1.34 DTT
-
Sinapis alba
1.1.1.34 DTT
-
Ipomoea batatas
1.1.1.34 DTT
-
Malus domestica
1.1.1.34 DTT
-
Dunaliella salina
1.1.1.34 DTT
-
Euphorbia lathyris
1.1.1.34 DTT
-
Nepeta cataria
1.1.1.34 DTT
-
Pimpinella anisum
1.1.1.34 DTT
-
Parthenium argentatum
1.1.1.34 DTT
-
Gossypium barbadense
1.1.1.34 DTT
-
Artemisia annua
1.1.1.34 DTT
-
Nicotiana benthamiana
1.1.1.34 DTT
-
Stevia rebaudiana
1.1.1.34 DTT
-
Salvia miltiorrhiza
1.1.1.34 DTT
-
Taraxacum brevicorniculatum
1.1.1.34 DTT
-
Solanum virginianum
1.1.1.34 DTT
-
Bixa orellana
1.1.1.34 EDTA increases the apparent HMGR activity in sweet potato extracts Ipomoea batatas

Inhibitors

EC Number Inhibitors Comment Organism Structure
1.1.1.34 EDTA inhibits the subsequent reactions of the mevalonate pathway in Hevea latex Hevea brasiliensis

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining
1.1.1.34 endoplasmic reticulum membrane
-
Vigna radiata var. radiata 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Hordeum vulgare 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Spinacia oleracea 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Pisum sativum 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Zea mays 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Solanum tuberosum 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Nicotiana tabacum 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Glycine max 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Lithospermum erythrorhizon 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Picea abies 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Brassica napus 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Arachis hypogaea 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Medicago sativa 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Daucus carota 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Solanum lycopersicum 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Helianthus tuberosus 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Raphanus sativus 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Gossypium hirsutum 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Ochromonas malhamensis 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Hevea brasiliensis 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Persea americana 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Cucumis melo 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Cannabis sativa 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Sinapis alba 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Ipomoea batatas 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Malus domestica 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Dunaliella salina 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Euphorbia lathyris 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Nepeta cataria 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Pimpinella anisum 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Parthenium argentatum 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Gossypium barbadense 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Artemisia annua 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Nicotiana benthamiana 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Stevia rebaudiana 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Salvia miltiorrhiza 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Taraxacum brevicorniculatum 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Solanum virginianum 5789
-
1.1.1.34 endoplasmic reticulum membrane
-
Bixa orellana 5789
-
1.1.1.34 endoplasmic reticulum membrane the enzyme spans the endoplasmic reticulum membrane twice. Both the N-terminal region and the highly conserved catalytic domain are in the cytosol, whereas only a short stretch of the protein is in the endoplasmic reticulum lumen. Insertion in the endoplasmic reticulum membrane is mediated by the signal recognition particle (SRP) that recognizes the two hydrophobic sequences which will become membrane spanning segments Arabidopsis thaliana 5789
-
1.1.1.34 microsome the HMGR activity is detected in the final microsomal pellet after ultracentrifugation Arabidopsis thaliana
-
-

Metals/Ions

EC Number Metals/Ions Comment Organism Structure
1.1.1.34 Ca2+ activates Vigna radiata var. radiata
1.1.1.34 Ca2+ activates Hordeum vulgare
1.1.1.34 Ca2+ activates Spinacia oleracea
1.1.1.34 Ca2+ activates Pisum sativum
1.1.1.34 Ca2+ activates Zea mays
1.1.1.34 Ca2+ activates Solanum tuberosum
1.1.1.34 Ca2+ activates Nicotiana tabacum
1.1.1.34 Ca2+ activates Glycine max
1.1.1.34 Ca2+ activates Lithospermum erythrorhizon
1.1.1.34 Ca2+ activates Arabidopsis thaliana
1.1.1.34 Ca2+ activates Picea abies
1.1.1.34 Ca2+ activates Brassica napus
1.1.1.34 Ca2+ activates Arachis hypogaea
1.1.1.34 Ca2+ activates Medicago sativa
1.1.1.34 Ca2+ activates Daucus carota
1.1.1.34 Ca2+ activates Solanum lycopersicum
1.1.1.34 Ca2+ activates Helianthus tuberosus
1.1.1.34 Ca2+ activates Raphanus sativus
1.1.1.34 Ca2+ activates Gossypium hirsutum
1.1.1.34 Ca2+ activates Ochromonas malhamensis
1.1.1.34 Ca2+ activates Hevea brasiliensis
1.1.1.34 Ca2+ activates Persea americana
1.1.1.34 Ca2+ activates Cucumis melo
1.1.1.34 Ca2+ activates Cannabis sativa
1.1.1.34 Ca2+ activates Sinapis alba
1.1.1.34 Ca2+ activates Ipomoea batatas
1.1.1.34 Ca2+ activates Malus domestica
1.1.1.34 Ca2+ activates Dunaliella salina
1.1.1.34 Ca2+ activates Euphorbia lathyris
1.1.1.34 Ca2+ activates Nepeta cataria
1.1.1.34 Ca2+ activates Pimpinella anisum
1.1.1.34 Ca2+ activates Parthenium argentatum
1.1.1.34 Ca2+ activates Gossypium barbadense
1.1.1.34 Ca2+ activates Artemisia annua
1.1.1.34 Ca2+ activates Nicotiana benthamiana
1.1.1.34 Ca2+ activates Stevia rebaudiana
1.1.1.34 Ca2+ activates Salvia miltiorrhiza
1.1.1.34 Ca2+ activates Taraxacum brevicorniculatum
1.1.1.34 Ca2+ activates Solanum virginianum
1.1.1.34 Ca2+ activates Bixa orellana

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Vigna radiata var. radiata
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Hordeum vulgare
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Spinacia oleracea
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Pisum sativum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Zea mays
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Solanum tuberosum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Nicotiana tabacum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Glycine max
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Lithospermum erythrorhizon
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Arabidopsis thaliana
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Picea abies
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Brassica napus
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Arachis hypogaea
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Medicago sativa
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Daucus carota
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Solanum lycopersicum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Helianthus tuberosus
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Raphanus sativus
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Gossypium hirsutum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Ochromonas malhamensis
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Hevea brasiliensis
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Persea americana
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Cucumis melo
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Cannabis sativa
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Sinapis alba
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Ipomoea batatas
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Malus domestica
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Dunaliella salina
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Euphorbia lathyris
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Nepeta cataria
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Pimpinella anisum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Parthenium argentatum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Gossypium barbadense
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Artemisia annua
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Nicotiana benthamiana
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Stevia rebaudiana
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Salvia miltiorrhiza
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Taraxacum brevicorniculatum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Solanum virginianum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+ Bixa orellana
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Vigna radiata var. radiata
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Hordeum vulgare
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Spinacia oleracea
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Pisum sativum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Zea mays
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Solanum tuberosum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Nicotiana tabacum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Glycine max
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Lithospermum erythrorhizon
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Arabidopsis thaliana
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Picea abies
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Brassica napus
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Arachis hypogaea
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Medicago sativa
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Daucus carota
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Solanum lycopersicum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Helianthus tuberosus
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Raphanus sativus
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Gossypium hirsutum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Ochromonas malhamensis
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Hevea brasiliensis
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Persea americana
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Cucumis melo
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Cannabis sativa
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Sinapis alba
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Ipomoea batatas
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Malus domestica
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Dunaliella salina
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Euphorbia lathyris
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Nepeta cataria
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Pimpinella anisum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Parthenium argentatum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Gossypium barbadense
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Artemisia annua
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Nicotiana benthamiana
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Stevia rebaudiana
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Salvia miltiorrhiza
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Taraxacum brevicorniculatum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Solanum virginianum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Bixa orellana
-
(R)-mevalonate + CoA + 2 NADP+
-
r

Organism

EC Number Organism UniProt Comment Textmining
1.1.1.34 Arabidopsis thaliana
-
-
-
1.1.1.34 Arachis hypogaea
-
-
-
1.1.1.34 Artemisia annua
-
-
-
1.1.1.34 Bixa orellana
-
-
-
1.1.1.34 Brassica napus
-
-
-
1.1.1.34 Cannabis sativa
-
-
-
1.1.1.34 Cucumis melo
-
-
-
1.1.1.34 Daucus carota
-
-
-
1.1.1.34 Dunaliella salina
-
-
-
1.1.1.34 Euphorbia lathyris
-
-
-
1.1.1.34 Glycine max
-
-
-
1.1.1.34 Gossypium barbadense
-
-
-
1.1.1.34 Gossypium hirsutum
-
-
-
1.1.1.34 Helianthus tuberosus
-
-
-
1.1.1.34 Hevea brasiliensis
-
-
-
1.1.1.34 Hordeum vulgare
-
-
-
1.1.1.34 Ipomoea batatas
-
-
-
1.1.1.34 Lithospermum erythrorhizon
-
-
-
1.1.1.34 Malus domestica
-
-
-
1.1.1.34 Medicago sativa
-
-
-
1.1.1.34 Nepeta cataria
-
-
-
1.1.1.34 Nicotiana benthamiana
-
-
-
1.1.1.34 Nicotiana tabacum
-
-
-
1.1.1.34 Ochromonas malhamensis
-
-
-
1.1.1.34 Parthenium argentatum
-
-
-
1.1.1.34 Persea americana
-
-
-
1.1.1.34 Picea abies
-
-
-
1.1.1.34 Pimpinella anisum
-
-
-
1.1.1.34 Pisum sativum
-
-
-
1.1.1.34 Raphanus sativus
-
-
-
1.1.1.34 Salvia miltiorrhiza
-
-
-
1.1.1.34 Sinapis alba
-
-
-
1.1.1.34 Solanum lycopersicum
-
-
-
1.1.1.34 Solanum tuberosum
-
-
-
1.1.1.34 Solanum virginianum
-
-
-
1.1.1.34 Spinacia oleracea
-
-
-
1.1.1.34 Stevia rebaudiana
-
-
-
1.1.1.34 Taraxacum brevicorniculatum
-
-
-
1.1.1.34 Vigna radiata var. radiata
-
-
-
1.1.1.34 Zea mays
-
-
-

Oxidation Stability

EC Number Oxidation Stability Organism
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Vigna radiata var. radiata
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Hordeum vulgare
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Spinacia oleracea
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Pisum sativum
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Zea mays
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Solanum tuberosum
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Nicotiana tabacum
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Glycine max
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Lithospermum erythrorhizon
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Arabidopsis thaliana
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Picea abies
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Brassica napus
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Arachis hypogaea
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Medicago sativa
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Daucus carota
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Solanum lycopersicum
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Helianthus tuberosus
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Raphanus sativus
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Gossypium hirsutum
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Ochromonas malhamensis
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Hevea brasiliensis
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Persea americana
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Cucumis melo
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Cannabis sativa
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Sinapis alba
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Ipomoea batatas
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Malus domestica
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Dunaliella salina
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Euphorbia lathyris
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Nepeta cataria
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Pimpinella anisum
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Parthenium argentatum
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Gossypium barbadense
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Artemisia annua
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Nicotiana benthamiana
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Stevia rebaudiana
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Salvia miltiorrhiza
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Taraxacum brevicorniculatum
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Solanum virginianum
1.1.1.34 the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Bixa orellana

Posttranslational Modification

EC Number Posttranslational Modification Comment Organism
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Vigna radiata var. radiata
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Hordeum vulgare
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Spinacia oleracea
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Pisum sativum
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Zea mays
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Solanum tuberosum
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Nicotiana tabacum
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Glycine max
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Lithospermum erythrorhizon
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Arabidopsis thaliana
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Picea abies
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Brassica napus
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Arachis hypogaea
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Medicago sativa
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Daucus carota
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Solanum lycopersicum
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Helianthus tuberosus
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Raphanus sativus
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Gossypium hirsutum
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Ochromonas malhamensis
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Hevea brasiliensis
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Persea americana
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Cucumis melo
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Cannabis sativa
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Sinapis alba
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Ipomoea batatas
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Malus domestica
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Dunaliella salina
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Euphorbia lathyris
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Nepeta cataria
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Pimpinella anisum
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Parthenium argentatum
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Gossypium barbadense
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Artemisia annua
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Nicotiana benthamiana
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Stevia rebaudiana
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Salvia miltiorrhiza
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Taraxacum brevicorniculatum
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Solanum virginianum
1.1.1.34 additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Bixa orellana
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Vigna radiata var. radiata
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Hordeum vulgare
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Spinacia oleracea
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Pisum sativum
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Zea mays
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Solanum tuberosum
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Nicotiana tabacum
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Glycine max
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Lithospermum erythrorhizon
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Arabidopsis thaliana
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Picea abies
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Brassica napus
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Arachis hypogaea
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Medicago sativa
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Daucus carota
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Solanum lycopersicum
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Helianthus tuberosus
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Raphanus sativus
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Gossypium hirsutum
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Ochromonas malhamensis
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Hevea brasiliensis
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Persea americana
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Cucumis melo
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Cannabis sativa
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Sinapis alba
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Ipomoea batatas
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Malus domestica
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Dunaliella salina
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Euphorbia lathyris
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Nepeta cataria
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Pimpinella anisum
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Parthenium argentatum
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Gossypium barbadense
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Artemisia annua
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Nicotiana benthamiana
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Stevia rebaudiana
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Salvia miltiorrhiza
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Taraxacum brevicorniculatum
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Solanum virginianum
1.1.1.34 phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Bixa orellana

Purification (Commentary)

EC Number Purification (Comment) Organism
1.1.1.34 native enzyme by ultracentrifugation Arabidopsis thaliana

Source Tissue

EC Number Source Tissue Comment Organism Textmining
1.1.1.34 bark
-
Parthenium argentatum
-
1.1.1.34 BY-2 cell
-
Nicotiana tabacum
-
1.1.1.34 callus
-
Nicotiana tabacum
-
1.1.1.34 callus
-
Picea abies
-
1.1.1.34 callus
-
Nepeta cataria
-
1.1.1.34 callus
-
Bixa orellana
-
1.1.1.34 cell culture
-
Nicotiana tabacum
-
1.1.1.34 cell culture
-
Glycine max
-
1.1.1.34 cell culture
-
Lithospermum erythrorhizon
-
1.1.1.34 cell culture
-
Picea abies
-
1.1.1.34 cell culture
-
Daucus carota
-
1.1.1.34 cell culture
-
Ochromonas malhamensis
-
1.1.1.34 cell culture
-
Dunaliella salina
-
1.1.1.34 cell culture
-
Pimpinella anisum
-
1.1.1.34 cell suspension culture
-
Solanum virginianum
-
1.1.1.34 cotyledon
-
Glycine max
-
1.1.1.34 exocarp
-
Malus domestica
-
1.1.1.34 fruit
-
Solanum lycopersicum
-
1.1.1.34 fruit
-
Cucumis melo
-
1.1.1.34 hairy root
-
Lithospermum erythrorhizon
-
1.1.1.34 hairy root
-
Medicago sativa
-
1.1.1.34 hairy root
-
Salvia miltiorrhiza
-
1.1.1.34 hypocotyl
-
Glycine max
-
1.1.1.34 KY-14 cell
-
Nicotiana tabacum
-
1.1.1.34 latex
-
Hevea brasiliensis
-
1.1.1.34 latex
-
Euphorbia lathyris
-
1.1.1.34 latex
-
Taraxacum brevicorniculatum
-
1.1.1.34 leaf
-
Vigna radiata var. radiata
-
1.1.1.34 leaf
-
Spinacia oleracea
-
1.1.1.34 leaf
-
Picea abies
-
1.1.1.34 leaf
-
Solanum lycopersicum
-
1.1.1.34 leaf
-
Cannabis sativa
-
1.1.1.34 leaf
-
Euphorbia lathyris
-
1.1.1.34 leaf
-
Nepeta cataria
-
1.1.1.34 leaf
-
Artemisia annua
-
1.1.1.34 leaf
-
Nicotiana benthamiana
-
1.1.1.34 leaf
-
Stevia rebaudiana
-
1.1.1.34 leaf
-
Bixa orellana
-
1.1.1.34 leaf expanded Nicotiana tabacum
-
1.1.1.34 leaf fully expanded Parthenium argentatum
-
1.1.1.34 leaf rosette leaves and fully expanded leaves Arabidopsis thaliana
-
1.1.1.34 mesocarp
-
Persea americana
-
1.1.1.34 pericarp
-
Cucumis melo
-
1.1.1.34 root
-
Glycine max
-
1.1.1.34 root
-
Ipomoea batatas
-
1.1.1.34 seed
-
Arabidopsis thaliana
-
1.1.1.34 seed
-
Persea americana
-
1.1.1.34 seed developing Nicotiana tabacum
-
1.1.1.34 seed developing Brassica napus
-
1.1.1.34 seedling
-
Hordeum vulgare
-
1.1.1.34 seedling
-
Picea abies
-
1.1.1.34 seedling
-
Raphanus sativus
-
1.1.1.34 seedling etiolated Zea mays
-
1.1.1.34 seedling green Arachis hypogaea
-
1.1.1.34 seedling green Sinapis alba
-
1.1.1.34 seedling aerial part and full seedling Nicotiana tabacum
-
1.1.1.34 seedling apical part Glycine max
-
1.1.1.34 seedling etiolated and green seedlings Pisum sativum
-
1.1.1.34 seedling green seedling, aerial part and root Arabidopsis thaliana
-
1.1.1.34 stele
-
Gossypium hirsutum
-
1.1.1.34 stele
-
Gossypium barbadense
-
1.1.1.34 stem
-
Euphorbia lathyris
-
1.1.1.34 stem lower Parthenium argentatum
-
1.1.1.34 tuber
-
Solanum tuberosum
-
1.1.1.34 tuber explants Helianthus tuberosus
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Vigna radiata var. radiata (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Hordeum vulgare (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Spinacia oleracea (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Pisum sativum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Zea mays (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Solanum tuberosum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Nicotiana tabacum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Glycine max (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Lithospermum erythrorhizon (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Arabidopsis thaliana (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Picea abies (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Brassica napus (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Arachis hypogaea (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Medicago sativa (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Daucus carota (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Solanum lycopersicum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Helianthus tuberosus (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Raphanus sativus (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Gossypium hirsutum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Ochromonas malhamensis (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Hevea brasiliensis (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Persea americana (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Cucumis melo (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Cannabis sativa (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Sinapis alba (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Ipomoea batatas (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Malus domestica (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Dunaliella salina (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Euphorbia lathyris (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Nepeta cataria (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Pimpinella anisum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Parthenium argentatum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Gossypium barbadense (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Artemisia annua (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Nicotiana benthamiana (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Stevia rebaudiana (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Salvia miltiorrhiza (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Taraxacum brevicorniculatum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Solanum virginianum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (R)-mevalonate + CoA + 2 NADP+
-
Bixa orellana (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Vigna radiata var. radiata (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Hordeum vulgare (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Spinacia oleracea (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Pisum sativum (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Zea mays (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Solanum tuberosum (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Nicotiana tabacum (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Glycine max (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Lithospermum erythrorhizon (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Arabidopsis thaliana (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Picea abies (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Brassica napus (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Arachis hypogaea (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Medicago sativa (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Daucus carota (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Solanum lycopersicum (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Helianthus tuberosus (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Raphanus sativus (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Gossypium hirsutum (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Ochromonas malhamensis (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Hevea brasiliensis (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Persea americana (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Cucumis melo (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Cannabis sativa (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Sinapis alba (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Ipomoea batatas (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Malus domestica (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Dunaliella salina (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Euphorbia lathyris (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Nepeta cataria (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Pimpinella anisum (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Parthenium argentatum (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Gossypium barbadense (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Artemisia annua (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Nicotiana benthamiana (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Stevia rebaudiana (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Salvia miltiorrhiza (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Taraxacum brevicorniculatum (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Solanum virginianum (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Bixa orellana (R)-mevalonate + CoA + 2 NADP+
-
r
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Vigna radiata var. radiata ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Hordeum vulgare ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Spinacia oleracea ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Pisum sativum ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Zea mays ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Solanum tuberosum ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Nicotiana tabacum ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Glycine max ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Lithospermum erythrorhizon ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Arabidopsis thaliana ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Picea abies ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Brassica napus ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Arachis hypogaea ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Medicago sativa ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Daucus carota ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Solanum lycopersicum ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Helianthus tuberosus ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Raphanus sativus ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Gossypium hirsutum ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Ochromonas malhamensis ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Hevea brasiliensis ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Persea americana ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Cucumis melo ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Cannabis sativa ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Sinapis alba ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Ipomoea batatas ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Malus domestica ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Dunaliella salina ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Euphorbia lathyris ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Nepeta cataria ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Pimpinella anisum ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Parthenium argentatum ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Gossypium barbadense ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Artemisia annua ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Nicotiana benthamiana ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Stevia rebaudiana ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Salvia miltiorrhiza ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Taraxacum brevicorniculatum ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Solanum virginianum ?
-
?
1.1.1.34 additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Bixa orellana ?
-
?

Subunits

EC Number Subunits Comment Organism
1.1.1.34 ? x * 63000-70000 Vigna radiata var. radiata
1.1.1.34 ? x * 63000-70000 Hordeum vulgare
1.1.1.34 ? x * 63000-70000 Spinacia oleracea
1.1.1.34 ? x * 63000-70000 Pisum sativum
1.1.1.34 ? x * 63000-70000 Zea mays
1.1.1.34 ? x * 63000-70000 Solanum tuberosum
1.1.1.34 ? x * 63000-70000 Nicotiana tabacum
1.1.1.34 ? x * 63000-70000 Glycine max
1.1.1.34 ? x * 63000-70000 Lithospermum erythrorhizon
1.1.1.34 ? x * 63000-70000 Arabidopsis thaliana
1.1.1.34 ? x * 63000-70000 Picea abies
1.1.1.34 ? x * 63000-70000 Brassica napus
1.1.1.34 ? x * 63000-70000 Arachis hypogaea
1.1.1.34 ? x * 63000-70000 Medicago sativa
1.1.1.34 ? x * 63000-70000 Daucus carota
1.1.1.34 ? x * 63000-70000 Solanum lycopersicum
1.1.1.34 ? x * 63000-70000 Helianthus tuberosus
1.1.1.34 ? x * 63000-70000 Raphanus sativus
1.1.1.34 ? x * 63000-70000 Gossypium hirsutum
1.1.1.34 ? x * 63000-70000 Ochromonas malhamensis
1.1.1.34 ? x * 63000-70000 Hevea brasiliensis
1.1.1.34 ? x * 63000-70000 Persea americana
1.1.1.34 ? x * 63000-70000 Cucumis melo
1.1.1.34 ? x * 63000-70000 Cannabis sativa
1.1.1.34 ? x * 63000-70000 Sinapis alba
1.1.1.34 ? x * 63000-70000 Ipomoea batatas
1.1.1.34 ? x * 63000-70000 Malus domestica
1.1.1.34 ? x * 63000-70000 Dunaliella salina
1.1.1.34 ? x * 63000-70000 Euphorbia lathyris
1.1.1.34 ? x * 63000-70000 Nepeta cataria
1.1.1.34 ? x * 63000-70000 Pimpinella anisum
1.1.1.34 ? x * 63000-70000 Parthenium argentatum
1.1.1.34 ? x * 63000-70000 Gossypium barbadense
1.1.1.34 ? x * 63000-70000 Artemisia annua
1.1.1.34 ? x * 63000-70000 Nicotiana benthamiana
1.1.1.34 ? x * 63000-70000 Stevia rebaudiana
1.1.1.34 ? x * 63000-70000 Salvia miltiorrhiza
1.1.1.34 ? x * 63000-70000 Taraxacum brevicorniculatum
1.1.1.34 ? x * 63000-70000 Solanum virginianum
1.1.1.34 ? x * 63000-70000 Bixa orellana

Synonyms

EC Number Synonyms Comment Organism
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Vigna radiata var. radiata
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Hordeum vulgare
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Spinacia oleracea
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Pisum sativum
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Zea mays
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Solanum tuberosum
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Nicotiana tabacum
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Glycine max
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Lithospermum erythrorhizon
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Arabidopsis thaliana
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Picea abies
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Brassica napus
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Arachis hypogaea
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Medicago sativa
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Daucus carota
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Solanum lycopersicum
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Helianthus tuberosus
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Raphanus sativus
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Gossypium hirsutum
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Ochromonas malhamensis
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Hevea brasiliensis
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Persea americana
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Cucumis melo
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Cannabis sativa
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Sinapis alba
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Ipomoea batatas
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Malus domestica
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Dunaliella salina
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Euphorbia lathyris
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Nepeta cataria
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Pimpinella anisum
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Parthenium argentatum
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Gossypium barbadense
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Artemisia annua
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Nicotiana benthamiana
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Stevia rebaudiana
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Salvia miltiorrhiza
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Taraxacum brevicorniculatum
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Solanum virginianum
1.1.1.34 3-hydroxy-3-methylglutaryl CoA reductase
-
Bixa orellana
1.1.1.34 HMGR
-
Vigna radiata var. radiata
1.1.1.34 HMGR
-
Hordeum vulgare
1.1.1.34 HMGR
-
Spinacia oleracea
1.1.1.34 HMGR
-
Pisum sativum
1.1.1.34 HMGR
-
Zea mays
1.1.1.34 HMGR
-
Solanum tuberosum
1.1.1.34 HMGR
-
Nicotiana tabacum
1.1.1.34 HMGR
-
Glycine max
1.1.1.34 HMGR
-
Lithospermum erythrorhizon
1.1.1.34 HMGR
-
Arabidopsis thaliana
1.1.1.34 HMGR
-
Picea abies
1.1.1.34 HMGR
-
Brassica napus
1.1.1.34 HMGR
-
Arachis hypogaea
1.1.1.34 HMGR
-
Medicago sativa
1.1.1.34 HMGR
-
Daucus carota
1.1.1.34 HMGR
-
Solanum lycopersicum
1.1.1.34 HMGR
-
Helianthus tuberosus
1.1.1.34 HMGR
-
Raphanus sativus
1.1.1.34 HMGR
-
Gossypium hirsutum
1.1.1.34 HMGR
-
Ochromonas malhamensis
1.1.1.34 HMGR
-
Hevea brasiliensis
1.1.1.34 HMGR
-
Persea americana
1.1.1.34 HMGR
-
Cucumis melo
1.1.1.34 HMGR
-
Cannabis sativa
1.1.1.34 HMGR
-
Sinapis alba
1.1.1.34 HMGR
-
Ipomoea batatas
1.1.1.34 HMGR
-
Malus domestica
1.1.1.34 HMGR
-
Dunaliella salina
1.1.1.34 HMGR
-
Euphorbia lathyris
1.1.1.34 HMGR
-
Nepeta cataria
1.1.1.34 HMGR
-
Pimpinella anisum
1.1.1.34 HMGR
-
Parthenium argentatum
1.1.1.34 HMGR
-
Gossypium barbadense
1.1.1.34 HMGR
-
Artemisia annua
1.1.1.34 HMGR
-
Nicotiana benthamiana
1.1.1.34 HMGR
-
Stevia rebaudiana
1.1.1.34 HMGR
-
Salvia miltiorrhiza
1.1.1.34 HMGR
-
Taraxacum brevicorniculatum
1.1.1.34 HMGR
-
Solanum virginianum
1.1.1.34 HMGR
-
Bixa orellana

Temperature Optimum [°C]

EC Number Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
1.1.1.34 37
-
assay at Vigna radiata var. radiata
1.1.1.34 37
-
assay at Hordeum vulgare
1.1.1.34 37
-
assay at Spinacia oleracea
1.1.1.34 37
-
assay at Pisum sativum
1.1.1.34 37
-
assay at Zea mays
1.1.1.34 37
-
assay at Solanum tuberosum
1.1.1.34 37
-
assay at Nicotiana tabacum
1.1.1.34 37
-
assay at Glycine max
1.1.1.34 37
-
assay at Lithospermum erythrorhizon
1.1.1.34 37
-
assay at Arabidopsis thaliana
1.1.1.34 37
-
assay at Picea abies
1.1.1.34 37
-
assay at Brassica napus
1.1.1.34 37
-
assay at Arachis hypogaea
1.1.1.34 37
-
assay at Medicago sativa
1.1.1.34 37
-
assay at Daucus carota
1.1.1.34 37
-
assay at Solanum lycopersicum
1.1.1.34 37
-
assay at Helianthus tuberosus
1.1.1.34 37
-
assay at Raphanus sativus
1.1.1.34 37
-
assay at Gossypium hirsutum
1.1.1.34 37
-
assay at Ochromonas malhamensis
1.1.1.34 37
-
assay at Hevea brasiliensis
1.1.1.34 37
-
assay at Persea americana
1.1.1.34 37
-
assay at Cucumis melo
1.1.1.34 37
-
assay at Cannabis sativa
1.1.1.34 37
-
assay at Sinapis alba
1.1.1.34 37
-
assay at Ipomoea batatas
1.1.1.34 37
-
assay at Malus domestica
1.1.1.34 37
-
assay at Dunaliella salina
1.1.1.34 37
-
assay at Euphorbia lathyris
1.1.1.34 37
-
assay at Nepeta cataria
1.1.1.34 37
-
assay at Pimpinella anisum
1.1.1.34 37
-
assay at Parthenium argentatum
1.1.1.34 37
-
assay at Gossypium barbadense
1.1.1.34 37
-
assay at Artemisia annua
1.1.1.34 37
-
assay at Nicotiana benthamiana
1.1.1.34 37
-
assay at Stevia rebaudiana
1.1.1.34 37
-
assay at Salvia miltiorrhiza
1.1.1.34 37
-
assay at Taraxacum brevicorniculatum
1.1.1.34 37
-
assay at Solanum virginianum
1.1.1.34 37
-
assay at Bixa orellana

pH Optimum

EC Number pH Optimum Minimum pH Optimum Maximum Comment Organism
1.1.1.34 additional information
-
two pH optima are found, corresponding to HMGR from the heavy or the light fractions: pH 7.0 and pH 75, respectively Parthenium argentatum
1.1.1.34 additional information
-
two pH optima are found, corresponding to HMGR from the heavy or the light fractions: pH 7.9 and pH 6.9, respectively Pisum sativum
1.1.1.34 6.8
-
-
Hevea brasiliensis
1.1.1.34 6.9
-
-
Pisum sativum
1.1.1.34 7
-
-
Parthenium argentatum
1.1.1.34 7.2
-
assay at Vigna radiata var. radiata
1.1.1.34 7.2
-
assay at Hordeum vulgare
1.1.1.34 7.2
-
assay at Spinacia oleracea
1.1.1.34 7.2
-
assay at Zea mays
1.1.1.34 7.2
-
assay at Solanum tuberosum
1.1.1.34 7.2
-
assay at Nicotiana tabacum
1.1.1.34 7.2
-
assay at Glycine max
1.1.1.34 7.2
-
assay at Lithospermum erythrorhizon
1.1.1.34 7.2
-
assay at Arabidopsis thaliana
1.1.1.34 7.2
-
assay at Picea abies
1.1.1.34 7.2
-
assay at Brassica napus
1.1.1.34 7.2
-
assay at Arachis hypogaea
1.1.1.34 7.2
-
assay at Medicago sativa
1.1.1.34 7.2
-
assay at Daucus carota
1.1.1.34 7.2
-
assay at Solanum lycopersicum
1.1.1.34 7.2
-
assay at Helianthus tuberosus
1.1.1.34 7.2
-
assay at Gossypium hirsutum
1.1.1.34 7.2
-
assay at Ochromonas malhamensis
1.1.1.34 7.2
-
assay at Persea americana
1.1.1.34 7.2
-
assay at Cucumis melo
1.1.1.34 7.2
-
assay at Cannabis sativa
1.1.1.34 7.2
-
assay at Sinapis alba
1.1.1.34 7.2
-
assay at Ipomoea batatas
1.1.1.34 7.2
-
assay at Malus domestica
1.1.1.34 7.2
-
assay at Dunaliella salina
1.1.1.34 7.2
-
assay at Euphorbia lathyris
1.1.1.34 7.2
-
assay at Nepeta cataria
1.1.1.34 7.2
-
assay at Pimpinella anisum
1.1.1.34 7.2
-
assay at Gossypium barbadense
1.1.1.34 7.2
-
assay at Artemisia annua
1.1.1.34 7.2
-
assay at Nicotiana benthamiana
1.1.1.34 7.2
-
assay at Stevia rebaudiana
1.1.1.34 7.2
-
assay at Salvia miltiorrhiza
1.1.1.34 7.2
-
assay at Taraxacum brevicorniculatum
1.1.1.34 7.2
-
assay at Solanum virginianum
1.1.1.34 7.2
-
assay at Bixa orellana
1.1.1.34 7.3 7.5
-
Raphanus sativus
1.1.1.34 7.5
-
-
Parthenium argentatum
1.1.1.34 7.9
-
-
Pisum sativum

Cofactor

EC Number Cofactor Comment Organism Structure
1.1.1.34 NADP+
-
Vigna radiata var. radiata
1.1.1.34 NADP+
-
Hordeum vulgare
1.1.1.34 NADP+
-
Spinacia oleracea
1.1.1.34 NADP+
-
Pisum sativum
1.1.1.34 NADP+
-
Zea mays
1.1.1.34 NADP+
-
Solanum tuberosum
1.1.1.34 NADP+
-
Nicotiana tabacum
1.1.1.34 NADP+
-
Glycine max
1.1.1.34 NADP+
-
Lithospermum erythrorhizon
1.1.1.34 NADP+
-
Arabidopsis thaliana
1.1.1.34 NADP+
-
Picea abies
1.1.1.34 NADP+
-
Brassica napus
1.1.1.34 NADP+
-
Arachis hypogaea
1.1.1.34 NADP+
-
Medicago sativa
1.1.1.34 NADP+
-
Daucus carota
1.1.1.34 NADP+
-
Solanum lycopersicum
1.1.1.34 NADP+
-
Helianthus tuberosus
1.1.1.34 NADP+
-
Raphanus sativus
1.1.1.34 NADP+
-
Gossypium hirsutum
1.1.1.34 NADP+
-
Ochromonas malhamensis
1.1.1.34 NADP+
-
Hevea brasiliensis
1.1.1.34 NADP+
-
Persea americana
1.1.1.34 NADP+
-
Cucumis melo
1.1.1.34 NADP+
-
Cannabis sativa
1.1.1.34 NADP+
-
Sinapis alba
1.1.1.34 NADP+
-
Ipomoea batatas
1.1.1.34 NADP+
-
Malus domestica
1.1.1.34 NADP+
-
Dunaliella salina
1.1.1.34 NADP+
-
Euphorbia lathyris
1.1.1.34 NADP+
-
Nepeta cataria
1.1.1.34 NADP+
-
Pimpinella anisum
1.1.1.34 NADP+
-
Parthenium argentatum
1.1.1.34 NADP+
-
Gossypium barbadense
1.1.1.34 NADP+
-
Artemisia annua
1.1.1.34 NADP+
-
Nicotiana benthamiana
1.1.1.34 NADP+
-
Stevia rebaudiana
1.1.1.34 NADP+
-
Salvia miltiorrhiza
1.1.1.34 NADP+
-
Taraxacum brevicorniculatum
1.1.1.34 NADP+
-
Solanum virginianum
1.1.1.34 NADP+
-
Bixa orellana
1.1.1.34 NADPH
-
Vigna radiata var. radiata
1.1.1.34 NADPH
-
Hordeum vulgare
1.1.1.34 NADPH
-
Spinacia oleracea
1.1.1.34 NADPH
-
Pisum sativum
1.1.1.34 NADPH
-
Zea mays
1.1.1.34 NADPH
-
Solanum tuberosum
1.1.1.34 NADPH
-
Nicotiana tabacum
1.1.1.34 NADPH
-
Glycine max
1.1.1.34 NADPH
-
Lithospermum erythrorhizon
1.1.1.34 NADPH
-
Arabidopsis thaliana
1.1.1.34 NADPH
-
Picea abies
1.1.1.34 NADPH
-
Brassica napus
1.1.1.34 NADPH
-
Arachis hypogaea
1.1.1.34 NADPH
-
Medicago sativa
1.1.1.34 NADPH
-
Daucus carota
1.1.1.34 NADPH
-
Solanum lycopersicum
1.1.1.34 NADPH
-
Helianthus tuberosus
1.1.1.34 NADPH
-
Raphanus sativus
1.1.1.34 NADPH
-
Gossypium hirsutum
1.1.1.34 NADPH
-
Ochromonas malhamensis
1.1.1.34 NADPH
-
Hevea brasiliensis
1.1.1.34 NADPH
-
Persea americana
1.1.1.34 NADPH
-
Cucumis melo
1.1.1.34 NADPH
-
Cannabis sativa
1.1.1.34 NADPH
-
Sinapis alba
1.1.1.34 NADPH
-
Ipomoea batatas
1.1.1.34 NADPH
-
Malus domestica
1.1.1.34 NADPH
-
Dunaliella salina
1.1.1.34 NADPH
-
Euphorbia lathyris
1.1.1.34 NADPH
-
Nepeta cataria
1.1.1.34 NADPH
-
Pimpinella anisum
1.1.1.34 NADPH
-
Parthenium argentatum
1.1.1.34 NADPH
-
Gossypium barbadense
1.1.1.34 NADPH
-
Artemisia annua
1.1.1.34 NADPH
-
Nicotiana benthamiana
1.1.1.34 NADPH
-
Stevia rebaudiana
1.1.1.34 NADPH
-
Salvia miltiorrhiza
1.1.1.34 NADPH
-
Taraxacum brevicorniculatum
1.1.1.34 NADPH
-
Solanum virginianum
1.1.1.34 NADPH
-
Bixa orellana

General Information

EC Number General Information Comment Organism
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Vigna radiata var. radiata
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Hordeum vulgare
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Spinacia oleracea
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Pisum sativum
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Zea mays
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Solanum tuberosum
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Nicotiana tabacum
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Glycine max
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Lithospermum erythrorhizon
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Arabidopsis thaliana
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Picea abies
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Brassica napus
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Arachis hypogaea
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Medicago sativa
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Daucus carota
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Solanum lycopersicum
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Helianthus tuberosus
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Raphanus sativus
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Gossypium hirsutum
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Ochromonas malhamensis
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Hevea brasiliensis
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Persea americana
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Cucumis melo
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Cannabis sativa
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Sinapis alba
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Ipomoea batatas
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Malus domestica
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Dunaliella salina
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Euphorbia lathyris
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Nepeta cataria
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Pimpinella anisum
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Parthenium argentatum
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Gossypium barbadense
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Artemisia annua
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Nicotiana benthamiana
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Stevia rebaudiana
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Salvia miltiorrhiza
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Taraxacum brevicorniculatum
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Solanum virginianum
1.1.1.34 evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Bixa orellana
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Vigna radiata var. radiata
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Hordeum vulgare
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Spinacia oleracea
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Pisum sativum
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Zea mays
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Solanum tuberosum
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Nicotiana tabacum
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Glycine max
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Lithospermum erythrorhizon
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Arabidopsis thaliana
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Picea abies
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Brassica napus
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Arachis hypogaea
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Medicago sativa
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Daucus carota
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Solanum lycopersicum
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Helianthus tuberosus
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Raphanus sativus
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Gossypium hirsutum
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Ochromonas malhamensis
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Hevea brasiliensis
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Persea americana
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Cucumis melo
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Cannabis sativa
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Sinapis alba
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Ipomoea batatas
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Malus domestica
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Dunaliella salina
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Euphorbia lathyris
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Nepeta cataria
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Pimpinella anisum
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Parthenium argentatum
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Gossypium barbadense
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Artemisia annua
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Nicotiana benthamiana
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Stevia rebaudiana
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Salvia miltiorrhiza
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Taraxacum brevicorniculatum
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Solanum virginianum
1.1.1.34 metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Bixa orellana
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Vigna radiata var. radiata
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Hordeum vulgare
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Spinacia oleracea
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Pisum sativum
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Zea mays
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Solanum tuberosum
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Nicotiana tabacum
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Glycine max
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Lithospermum erythrorhizon
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Picea abies
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Brassica napus
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Arachis hypogaea
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Medicago sativa
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Daucus carota
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Solanum lycopersicum
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Helianthus tuberosus
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Raphanus sativus
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Gossypium hirsutum
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Ochromonas malhamensis
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Hevea brasiliensis
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Persea americana
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Cucumis melo
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Cannabis sativa
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Sinapis alba
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Ipomoea batatas
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Malus domestica
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Dunaliella salina
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Euphorbia lathyris
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Nepeta cataria
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Pimpinella anisum
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Parthenium argentatum
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Gossypium barbadense
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Artemisia annua
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Nicotiana benthamiana
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Stevia rebaudiana
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Salvia miltiorrhiza
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Taraxacum brevicorniculatum
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Solanum virginianum
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Bixa orellana
1.1.1.34 physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated. Protein phosphatase 2A (PP2A) is both a transcriptional and a posttranslational regulator of HMGR in Arabidopsis thaliana Arabidopsis thaliana