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Literature summary extracted from

  • Manstein, D.J.; Pai, E.F.
    Absolute stereochemistry of flavins in enzyme-catalyzed reactions (1986), Biochemistry, 25, 6807-6816.
    View publication on PubMed

Organism

EC Number Organism UniProt Comment Textmining
1.14.13.4 Pseudomonas sp.
-
-
-
1.14.13.35 Cutaneotrichosporon cutaneum
-
yeast
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.14.13.4 3-(2-hydroxyphenyl)propanoate + NADH + O2
-
Pseudomonas sp. 3-(2,3-dihydroxyphenyl)propanoate + NAD+ + H2O
-
?
1.14.13.35 anthranilate + NADPH + O2
-
Cutaneotrichosporon cutaneum 2,3-dihydroxybenzoate + NADP+ + NH3
-
?

Cofactor

EC Number Cofactor Comment Organism Structure
1.14.13.4 NADH uses the re-face of the flavin ring Pseudomonas sp.
1.14.13.35 NADPH enzyme uses the re-face of the flavin ring Cutaneotrichosporon cutaneum