Enzyme

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     1. Oxidoreductases
        1.14 Acting on paired donors, with incorporation or reduction of molecular oxygen
            1.14.19 With oxidation of a pair of donors resulting in the reduction of O2 to two molecules of water
ID:1.14.19.50
Description:Noroxomaritidine synthase.
Alternative Name: CYP96T1.

3D structure

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References

External Links

UniProtKB Enzyme Link: UniProtKB 1.14.19.50
BRENDA Enzyme Link: BRENDA 1.14.19.50
KEGG Enzyme Link: KEGG1.14.19.50
BioCyc Enzyme Link: BioCyc 1.14.19.50
ExPASy Enzyme Link: ExPASy1.14.19.50
EC2PDB Enzyme Link: EC2PDB 1.14.19.50
ExplorEnz Enzyme Link: ExplorEnz 1.14.19.50
PRIAM enzyme-specific profiles Link: PRIAM 1.14.19.50
IntEnz Enzyme Link: IntEnz 1.14.19.50
MEDLINE Enzyme Link: MEDLINE 1.14.19.50
MSA:

1.14.19.50;

Phylogenetic Tree:

1.14.19.50;

Uniprot:
M-CSA:
RHEA:51264 4'-O-methylnorbelladine + O2 + reduced [NADPH--hemoprotein reductase] = (10bS,4aR)-noroxomaritidine + H(+) + 2 H2O + oxidized [NADPH--hemoprotein reductase]
RULE(radius=1) [*:1]-[N;H0;+0:2]1-[*:3]:[*:4]-[NH;+0:5]-[c;H0;+0:6](:[*:7]):[c;H0;+0:8]-1:[nH;+0:9]:[*:10].[*:11]:[cH;+0:12]:[*:13]-[*:14]-[NH;+0:15]-[*:16]-[*:17]-[c;H0;+0:18]1:[cH;+0:19]:[cH;+0:20]:[c;H0;+0:21](-[OH;+0:22]):[cH;+0:23]:[cH;+0:24]:1.[O;H0;+0:25]=[O;H0;+0:26]>>[*:1]-[n;H0;+0:2]1:[*:3]:[*:4]:[n;H0;+0:5]:[c;H0;+0:6](:[*:7])-[c;H0;+0:8]:1:[n;H0;+0:9]:[*:10].[*:11]:[c;H0;+0:12]1:[*:13]-[*:14]-[N;H0;+0:15]2-[*:16]-[*:17]-[C;H0;+0:18]-13-[CH;+0:24]=[CH;+0:23]-[C;H0;+0:21](=[O;H0;+0:22])-[CH2;+0:20]-[CH;+0:19]-2-3.[OH2;+0:25].[OH2;+0:26]
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References

TitleAuthorsDatePubMed ID
CYP96T1 of Narcissus sp. aff. pseudonarcissus Catalyzes Formation of the Para-Para' C-C Phenol Couple in the Amaryllidaceae Alkaloids.Kilgore MB, Augustin MM, May GD, Crow JA, Kutchan TM201626941773

RHEA:51260 4'-O-methylnorbelladine + O2 + reduced [NADPH--hemoprotein reductase] = (10bR,4aS)-noroxomaritidine + H(+) + 2 H2O + oxidized [NADPH--hemoprotein reductase]
RULE(radius=1) [*:1]-[N;H0;+0:2]1-[*:3]:[*:4]-[NH;+0:5]-[c;H0;+0:6](:[*:7]):[c;H0;+0:8]-1:[nH;+0:9]:[*:10].[*:11]:[cH;+0:12]:[*:13]-[*:14]-[NH;+0:15]-[*:16]-[*:17]-[c;H0;+0:18]1:[cH;+0:19]:[cH;+0:20]:[c;H0;+0:21](-[OH;+0:22]):[cH;+0:23]:[cH;+0:24]:1.[O;H0;+0:25]=[O;H0;+0:26]>>[*:1]-[n;H0;+0:2]1:[*:3]:[*:4]:[n;H0;+0:5]:[c;H0;+0:6](:[*:7])-[c;H0;+0:8]:1:[n;H0;+0:9]:[*:10].[*:11]:[c;H0;+0:12]1:[*:13]-[*:14]-[N;H0;+0:15]2-[*:16]-[*:17]-[C;H0;+0:18]-13-[CH;+0:24]=[CH;+0:23]-[C;H0;+0:21](=[O;H0;+0:22])-[CH2;+0:20]-[CH;+0:19]-2-3.[OH2;+0:25].[OH2;+0:26]
Reaction
Core-to-Core More
Core-to-Core More

References

TitleAuthorsDatePubMed ID
CYP96T1 of Narcissus sp. aff. pseudonarcissus Catalyzes Formation of the Para-Para' C-C Phenol Couple in the Amaryllidaceae Alkaloids.Kilgore MB, Augustin MM, May GD, Crow JA, Kutchan TM201626941773