Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary 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)

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

Organism

EC Number Organism UniProt Comment Textmining
1.1.3.46 Streptomyces sp. A0A0P0KG57
-
-
1.1.3.46 Streptomyces sp. DSM11171 A0A0P0KG57
-
-

Substrates and Products (Substrate)

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

Synonyms

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