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EC Number
Substrates
Commentary Substrates
Organism
Products
Commentary (Products)
Reversibility
1.3.3.17
(3-methyl)-butylmalonyl-CoA + O2
low specific activity
Aromatoleum aromaticum
?
-
?
1.3.3.17
(3-methyl)-butylmalonyl-CoA + O2
low specific activity
Aromatoleum aromaticum EbN1
?
-
?
1.3.3.17
benzylmalonyl-CoA + O2
-
Aromatoleum aromaticum
(E)-cinnamoyl-CoA + CO2 + H2O2
-
ir
1.3.3.17
benzylmalonyl-CoA + O2
high activity. The enzyme is enantiospecific in benzylmalonyl-CoA turnover
Aromatoleum aromaticum
(E)-cinnamoyl-CoA + CO2 + H2O2
-
ir
1.3.3.17
benzylmalonyl-CoA + O2
-
Aromatoleum aromaticum EbN1
(E)-cinnamoyl-CoA + CO2 + H2O2
-
ir
1.3.3.17
benzylmalonyl-CoA + O2
high activity. The enzyme is enantiospecific in benzylmalonyl-CoA turnover
Aromatoleum aromaticum EbN1
(E)-cinnamoyl-CoA + CO2 + H2O2
-
ir
1.3.3.17
butylmalonyl-CoA + O2
low specific activity
Aromatoleum aromaticum
?
-
?
1.3.3.17
butylmalonyl-CoA + O2
low specific activity
Aromatoleum aromaticum EbN1
?
-
?
1.3.3.17
hexylmalonyl-CoA + O2
low specific activity
Aromatoleum aromaticum
?
-
?
1.3.3.17
more
the enzyme is inert with ethylmalonyl-CoA, methylmalonyl-CoA and phenylpropionyl-CoA. The enzyme shows no activity with electron transfer flavoprotein or artificial dyes serving as electron acceptors like ferricenium cation or phenazine-methosulfate/dichlorophenyl-indophenol. The enzyme also does not convert cinnamoyl-CoA to either benzylmalonyl-CoA (with carboxylation) or phenylpropionyl-CoA (without carboxylation) by using dithionite-reduced benzyl or methyl viologen
Aromatoleum aromaticum
?
-
-
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