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1.14.14.167: (13S,14R)-13-O-acetyl-1-hydroxy-N-methylcanadine 8-hydroxylase

This is an abbreviated version!
For detailed information about (13S,14R)-13-O-acetyl-1-hydroxy-N-methylcanadine 8-hydroxylase, go to the full flat file.

Reaction

(13S,14R)-13-O-acetyl-1-hydroxy-N-methylcanadine
+
[reduced NADPH-hemoprotein reductase]
+
O2
=
(13S,14R)-13-O-acetyl-1,8-dihydroxy-N-methylcanadine
+
[oxidized NADPH-hemoprotein reductase]
+
H2O

Synonyms

1-hydroxy-13-O-acetyl-N-methylcanadine 8-hydroxylase, CYP82X1

ECTree

     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
                1.14.14.167 (13S,14R)-13-O-acetyl-1-hydroxy-N-methylcanadine 8-hydroxylase

Reference

Reference on EC 1.14.14.167 - (13S,14R)-13-O-acetyl-1-hydroxy-N-methylcanadine 8-hydroxylase

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REF.
AUTHORS
TITLE
JOURNAL
VOL.
PAGES
YEAR
ORGANISM (UNIPROT)
PUBMED ID
SOURCE
Dang, T.; Chen, X.; Facchini, P.
Acetylation serves as a protective group in noscapine biosynthesis in opium poppy
Nat. Chem. Biol.
11
104-106
2015
Papaver somniferum (I3V6B7)
Manually annotated by BRENDA team
Li, Y.; Smolke, C.
Engineering biosynthesis of the anticancer alkaloid noscapine in yeast
Nat. Commun.
7
12137
2016
Papaver somniferum (I3V6B7)
Manually annotated by BRENDA team
Li, Y.; Li, S.; Thodey, K.; Trenchard, I.; Cravens, A.; Smolke, C.
Complete biosynthesis of noscapine and halogenated alkaloids in yeast
Proc. Natl. Acad. Sci. USA
115
E3922-E3931
2018
Papaver somniferum (I3V6B7)
Manually annotated by BRENDA team