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EC Number
Substrates
Commentary Substrates
Organism
Products
Commentary (Products)
Reversibility
3.7.1.3
(2S)-2-amino-4-oxo-4-phenylbutanoic acid + H2O
the rate-determining step is Cbeta-Cgamma bond cleavage
Pseudomonas fluorescens
benzoate + L-alanine
-
?
3.7.1.3
(2S,3S)-erythro-beta-methyl-L-kynurenine
-
Pseudomonas fluorescens
?
-
?
3.7.1.3
(4R)-5-bromodihydro-L-kynurenine + H2O
slow substrate, no activity with (4S)-5-bromodihydro-L-kynurenine
Pseudomonas fluorescens
? + L-alanine
-
?
3.7.1.3
(4R)-dihydro-L-kynurenine + H2O
-
Pseudomonas fluorescens
2-aminobenzaldehyde + L-alanine
-
?
3.7.1.3
(alphaS,4R)-dihydrokynurenine + H2O
the (alphaS,4R) diastereomer is a slow substrate for a retro-aldol reaction, and the (alphaS,4S) isomer is a potent competitive inhibitor, proposed mechanism for reaction of dihydrokynurenine
Pseudomonas fluorescens
?
-
?
3.7.1.3
2-amino-4-(2-chlorophenyl)-4-oxobutanoic acid + H2O
-
Pseudomonas fluorescens
?
-
?
3.7.1.3
2-amino-4-(2-methoxyphenyl)-4-oxobutanoic acid + H2O
-
Pseudomonas fluorescens
?
-
?
3.7.1.3
2-amino-4-(4-methoxyphenyl)-4-oxobutanoic acid + H2O
-
Pseudomonas fluorescens
?
-
?
3.7.1.3
2-fluorobenzoyl-DL-alanine + H2O
-
Pseudomonas fluorescens
2-fluorobenzoate + beta-alanine
-
?
3.7.1.3
3,5-dibromo-L-kynurenine + H2O
-
Homo sapiens
3,5-dibromoanthranilate + DL-kynurenine
-
?
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