4.2.1.75: uroporphyrinogen-III synthase
This is an abbreviated version!
For detailed information about uroporphyrinogen-III synthase, go to the full flat file.
Word Map on EC 4.2.1.75
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4.2.1.75
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porphyria
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erythropoietic
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heme
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photosensitivity
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5-aminolevulinic
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tetrapyrrole
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coproporphyrins
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delta-aminolevulinic
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ferrochelatase
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pbgase
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mutilate
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erythrodontia
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transfusion-dependent
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protoporphyria
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hypertrichosis
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urologists
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coproporphyrinogen
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aymaras
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amerindian
- 4.2.1.75
- porphyria
-
erythropoietic
- heme
-
photosensitivity
-
5-aminolevulinic
- tetrapyrrole
- coproporphyrins
-
delta-aminolevulinic
-
ferrochelatase
-
pbgase
-
mutilate
-
erythrodontia
-
transfusion-dependent
- protoporphyria
-
hypertrichosis
-
urologists
- coproporphyrinogen
-
aymaras
-
amerindian
Reaction
Synonyms
CobA/HemD, Hydroxymethylbilane hydrolyase [cyclizing], hydroxymethylbilane hydrolyase, cyclizing, Isomerase, uroporphyrinogen, Porphobilinogenase, Synthase, uroporphyrinogen III co-, U3S, URO synthase, uro'gen III synthase, URO-synthase, UROIIIS, Uroporphyrinogen III co-synthase, Uroporphyrinogen III cosynthase, Uroporphyrinogen III synthase, Uroporphyrinogen isomerase, Uroporphyrinogen-III cosynthase, Uroporphyrinogen-III cosynthetase, uroporphyrinogen-III-synthase, UROS
ECTree
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Subunits
Subunits on EC 4.2.1.75 - uroporphyrinogen-III synthase
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monomer
additional information
additional information
observed interdomain flexibility might be important for catalysis, the active site is located between the domains
additional information
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observed interdomain flexibility might be important for catalysis, the active site is located between the domains
additional information
a helical region in the molecule is essential to retain the kinetic stability of the folded conformation
additional information
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a helical region in the molecule is essential to retain the kinetic stability of the folded conformation
additional information
mapping of the URO-synthase active site by NMR perturbation studies, modelling by by in silico docking, active site structure, overview
additional information
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mapping of the URO-synthase active site by NMR perturbation studies, modelling by by in silico docking, active site structure, overview