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Literature summary for 1.1.3.46 extracted from

  • Gonsior, M.; Muehlenweg, A.; Tietzmann, M.; Rausch, S.; Poch, A.; Suessmuth, R.D.
    Biosynthesis of the peptide antibiotic feglymycin by a linear nonribosomal peptide synthetase mechanism (2015), ChemBioChem, 16, 2610-2614.
    View publication on PubMed

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
(S)-4-hydroxymandelate + O2 Streptomyces sp.
-
2-(4-hydroxyphenyl)-2-oxoacetate + H2O2
-
?
(S)-4-hydroxymandelate + O2 Streptomyces sp. DSM11171
-
2-(4-hydroxyphenyl)-2-oxoacetate + H2O2
-
?

Organism

Organism UniProt Comment Textmining
Streptomyces sp. A0A0P0KG57
-
-
Streptomyces sp. DSM11171 A0A0P0KG57
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(S)-4-hydroxymandelate + O2
-
Streptomyces sp. 2-(4-hydroxyphenyl)-2-oxoacetate + H2O2
-
?
(S)-4-hydroxymandelate + O2
-
Streptomyces sp. DSM11171 2-(4-hydroxyphenyl)-2-oxoacetate + H2O2
-
?

Synonyms

Synonyms Comment Organism
fegC
-
Streptomyces sp.
HmO
-
Streptomyces sp.
p-hydroxymandelate oxidase
-
Streptomyces sp.