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EC Number
Substrates
Commentary Substrates
Organism
Products
Commentary (Products)
Reversibility
1.13.12.3
5-hydroxytryptophan + O2
at 17% the rate of that for L-tryptophan
Pseudomonas savastanoi
5-hydroxyindole-3-acetamide + CO2 + H2O
-
?
1.13.12.3
5-methyltryptophan + O2
-
Pseudomonas savastanoi
5-methylindole-3-acetamide + CO2 + H2O
-
?
1.13.12.3
L-tryptophan + O2
oxidative decarboxylation of L-tryptophan during the biosynthesis of indoleacetic acid
Pseudomonas savastanoi
?
-
?
1.13.12.3
more
no activity with: indole-3-pyruvate, indole-3-acetaldehyde, alpha-methyltryptophan, indole-3-acetic acid
Pseudomonas savastanoi
?
-
?
1.13.12.3
L-alanine + O2
-
Pseudomonas savastanoi
acetamide + CO2 + H2O
-
?
1.13.12.3
L-alanine + O2
oxidation of alanine occurs through a hydride transfer mechanism
Pseudomonas savastanoi
acetamide + CO2 + H2O
-
?
1.13.12.3
L-tryptophan + O2
-
Pseudomonas savastanoi
indole-3-acetamide + CO2 + H2O
-
?
1.13.12.3
L-tryptophan + O2
-
Agrobacterium rhizogenes
indole-3-acetamide + CO2 + H2O
-
?
1.13.12.3
L-tryptophan + O2
-
Agrobacterium tumefaciens
indole-3-acetamide + CO2 + H2O
-
?
1.13.12.3
L-tryptophan + O2
-
Rubrivivax benzoatilyticus
indole-3-acetamide + CO2 + H2O
-
?
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