1.14.14.40: phenylalanine N-monooxygenase
This is an abbreviated version!
For detailed information about phenylalanine N-monooxygenase, go to the full flat file.
Word Map on EC 1.14.14.40
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1.14.14.40
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glucosinolates
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aldoxime
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phenylacetaldoxime
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benzyl
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brassicales
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indole-3-acetaldoxime
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nitriles
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phenylacetic
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cyanogenic
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prunus
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benzylglucosinolate
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iaa
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indole-3-acetic
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synthesis
- 1.14.14.40
- glucosinolates
- aldoxime
- phenylacetaldoxime
-
benzyl
- brassicales
- indole-3-acetaldoxime
- nitriles
-
phenylacetic
-
cyanogenic
-
prunus
- benzylglucosinolate
- iaa
-
indole-3-acetic
- synthesis
Reaction
+ 2 [reduced NADPH-hemoprotein reductase] + 2 O2 = + 2 [oxidized NADPH-hemoprotein reductase] + + 3 H2O
Synonyms
CYP79A1, CYP79A2, CYP79D16, cytochrome P450 79D16, EC 1.14.13.124
ECTree
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Systematic Name
Systematic Name on EC 1.14.14.40 - phenylalanine N-monooxygenase
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L-phenylalanine,[reduced NADPH-hemoprotein reductase]:oxygen oxidoreductase (N-hydroxylating)
This cytochrome P-450 (heme-thiolate) enzyme, found in plants, catalyses two successive N-hydroxylations of L-phenylalanine, a committed step in the biosynthesis of benzylglucosinolate and the cyanogenic glucosides (R)-prunasin and (R)-amygdalin. The product of the two hydroxylations, N,N-dihydroxy-L-phenylalanine, is labile and undergoes dehydration followed by decarboxylation, producing an oxime. It is still not known whether the decarboxylation is spontaneous or catalysed by the enzyme.