KEGG Orthology (KO) [BR:ko00001]
09100 Metabolism
09109 Metabolism of terpenoids and polyketides
01052 Type I polyketide structures
K14366 eryF, CYP107A; 6-deoxyerythronolide B hydroxylase
00522 Biosynthesis of 12-, 14- and 16-membered macrolides
K14366 eryF, CYP107A; 6-deoxyerythronolide B hydroxylase
09180 Brite Hierarchies
09181 Protein families: metabolism
01008 Polyketide biosynthesis proteins
K14366 eryF, CYP107A; 6-deoxyerythronolide B hydroxylase
00199 Cytochrome P450
K14366 eryF, CYP107A; 6-deoxyerythronolide B hydroxylase
Enzymes [BR:ko01000]
1. Oxidoreductases
1.14 Acting on paired donors, with incorporation or reduction of molecular oxygen
1.14.15 With reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen into the other donor
1.14.15.35 6-deoxyerythronolide B hydroxylase
K14366 eryF, CYP107A; 6-deoxyerythronolide B hydroxylase
Polyketide biosynthesis proteins [BR:ko01008]
Polyketide tailoring proteins
Oxygenase
K14366 eryF, CYP107A; 6-deoxyerythronolide B hydroxylase
Cytochrome P450 [BR:ko00199]
Cytochrome P450, bacteria type
CYP107 family
K14366 eryF, CYP107A; 6-deoxyerythronolide B hydroxylase
6-deoxyerythronolide B hydroxylase;
DEB hydroxylase;
eryF (gene name);
P450(eryF);
CYP107A1
Class
Oxidoreductases;
Acting on paired donors, with incorporation or reduction of molecular oxygen;
With reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen into the other donor
erythronolide B [CPD:C06635];
oxidized ferredoxin [iron-sulfur] cluster [CPD:C00139];
H2O [CPD:C00001]
Comment
A cytochrome P-450 (heme-thiolate) protein isolated from the bacterium Saccharopolyspora erythraea. The enzyme is involved in the biosynthesis of the antibiotic erythromycin.
History
EC 1.14.15.35 created 2014 as EC 1.14.13.188, transferred 2018 to EC 1.14.15.35
Macrolide antibiotic biosynthesis: isolation and properties of two forms of 6-deoxyerythronolide B hydroxylase from Saccharopolyspora erythraea (Streptomyces erythreus).
Crystal structures of the ferrous dioxygen complex of wild-type cytochrome P450eryF and its mutants, A245S and A245T: investigation of the proton transfer system in P450eryF.
Enzymatic reactions [BR:br08201]
1. Oxidoreductase reactions
1.14 Acting on paired donors, with incorporation or reduction of molecular oxygen
1.14.15 With reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen into the other donor
1.14.15.35
R05270 6-Deoxyerythronolide B + 2 Reduced ferredoxin + 2 H+ + Oxygen <=> Erythronolide B + 2 Oxidized ferredoxin + H2O