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Literature summary for 1.14.13.242 extracted from

  • Chaiyen, P.; Brissette, P.; Ballou, D.P.; Massey, V.
    Unusual mechanism of oxygen atom transfer and product rearrangement in the catalytic reaction of 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase (1997), Biochemistry, 36, 8060-8070.
    View publication on PubMed

Organism

Organism UniProt Comment Textmining
Pseudomonas sp.
-
-
-

Reaction

Reaction Comment Organism Reaction ID
3-hydroxy-2-methylpyridine-5-carboxylate + NAD(P)H + H+ + O2 = 2-(acetamidomethylidene)succinate + NAD(P)+ the enzyme catalyzes both a classical hydroxylation and a subsequent unique hydrolysis of the hydroxylated substrate to yield the acyclic product Pseudomonas sp.

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3-hydroxy-2-methylpyridine-5-carboxylate + NADH + O2
-
Pseudomonas sp. 2-(acetamidomethylene)succinate + NAD(P)+
-
?
5-hydroxynicotinic acid + NADH + O2
-
Pseudomonas sp. ?
-
?

Cofactor

Cofactor Comment Organism Structure
NADH
-
Pseudomonas sp.