Enzyme

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     1. Oxidoreductases
        1.14 Acting on paired donors, with incorporation or reduction of molecular oxygen
            1.14.14 With reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen into the other donor
ID:1.14.14.40
Description:Phenylalanine N-monooxygenase.
Alternative Name: Phenylalanine N-hydroxylase.
CYP79D16.
CYP79A2.

3D structure

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References

External Links

UniProtKB Enzyme Link: UniProtKB 1.14.14.40
BRENDA Enzyme Link: BRENDA 1.14.14.40
KEGG Enzyme Link: KEGG1.14.14.40
BioCyc Enzyme Link: BioCyc 1.14.14.40
ExPASy Enzyme Link: ExPASy1.14.14.40
EC2PDB Enzyme Link: EC2PDB 1.14.14.40
ExplorEnz Enzyme Link: ExplorEnz 1.14.14.40
PRIAM enzyme-specific profiles Link: PRIAM 1.14.14.40
IntEnz Enzyme Link: IntEnz 1.14.14.40
MEDLINE Enzyme Link: MEDLINE 1.14.14.40
MSA:

1.14.14.40;

Phylogenetic Tree:

1.14.14.40;

Uniprot:
M-CSA:
RHEA:33263 L-phenylalanine + 2 O2 + 2 reduced [NADPH--hemoprotein reductase] = (E)-phenylacetaldehyde oxime + CO2 + 2 H(+) + 3 H2O + 2 oxidized [NADPH--hemoprotein reductase]
RULE(radius=1) [*:1]-[C;H0;+0:2]1=[CH;+0:3]-[N;H0;+0:4](-[*:5])-[CH;+0:6]=[CH;+0:7]-[CH2;+0:8]-1.[*:9]-[CH;+0:10](-[NH2;+0:11])-[C;H0;+0:12](=[*:13])-[OH;+0:14].[*:15]-[N;H0;+0:16]1-[CH;+0:17]=[C;H0;+0:18](-[*:19])-[CH2;+0:20]-[CH;+0:21]=[CH;+0:22]-1.[O;H0;+0:23]=[O;H0;+0:24].[O;H0;+0:25]=[O;H0;+0:26]>>[*:9]-[CH;+0:10]=[N;H0;+0:11]-[OH;+0:23].[*:1]-[c;H0;+0:2]1:[cH;+0:3]:[n+;H0:4](-[*:5]):[cH;+0:6]:[cH;+0:7]:[cH;+0:8]:1.[*:15]-[n+;H0:16]1:[cH;+0:17]:[c;H0;+0:18](-[*:19]):[cH;+0:20]:[cH;+0:21]:[cH;+0:22]:1.[*:13]=[C;H0;+0:12]=[O;H0;+0:14].[OH2;+0:24].[OH2;+0:25].[OH2;+0:26]
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References

TitleAuthorsDatePubMed ID
Identification and characterization of CYP79D16 and CYP71AN24 catalyzing the first and second steps in L-phenylalanine-derived cyanogenic glycoside biosynthesis in the Japanese apricot, Prunus mume Sieb. et Zucc.Yamaguchi T, Yamamoto K, Asano Y2014 Sep25015725
Cytochrome P450 CYP79A2 from Arabidopsis thaliana L. Catalyzes the conversion of L-phenylalanine to phenylacetaldoxime in the biosynthesis of benzylglucosinolate.Wittstock U, Halkier BA2000 May 1210799553