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EC Number
Substrates
Commentary Substrates
Organism
Products
Commentary (Products)
Reversibility
1.14.14.30
2-butylamine + FADH2 + O2
-
Streptomyces viridifaciens
N-(2-butyl)hydroxylamine + FAD + H2O
39% of the activity with 2-methylpropanamine
?
1.14.14.30
2-butylamine + FADH2 + O2
-
Streptomyces viridifaciens MG456-hF10
N-(2-butyl)hydroxylamine + FAD + H2O
39% of the activity with 2-methylpropanamine
?
1.14.14.30
2-methylpropanamine + FADH2 + O2
-
Streptomyces viridifaciens
N-hydroxy-2-methylpropan-1-amine + FAD + H2O
-
?
1.14.14.30
2-methylpropanamine + FADH2 + O2
-
Streptomyces viridifaciens MG456-hF10
N-hydroxy-2-methylpropan-1-amine + FAD + H2O
-
?
1.14.14.30
2-methylpropanamine + FMNH2 + O2
-
Streptomyces viridifaciens
N-hydroxy-2-methylpropan-1-amine + FMN + H2O
-
?
1.14.14.30
2-methylpropanamine + FMNH2 + O2
-
Streptomyces viridifaciens MG456-hF10
N-hydroxy-2-methylpropan-1-amine + FMN + H2O
-
?
1.14.14.30
benzylamine + FADH2 + O2
-
Streptomyces viridifaciens
N-(benzyl)hydroxylamine + FAD + H2O
61% of the activity with 2-methylpropanamine
?
1.14.14.30
benzylamine + FADH2 + O2
-
Streptomyces viridifaciens MG456-hF10
N-(benzyl)hydroxylamine + FAD + H2O
61% of the activity with 2-methylpropanamine
?
1.14.14.30
more
amine N-hydroxylase cannot carry out the reduction of the flavin cofactor. Rather, the reduced flavin is supplied by a separate flavin reductase. The mechanism for the hydroxylation is likely to proceed via the formation of a flavin 4a-hydroperoxide
Streptomyces viridifaciens
?
-
?
1.14.14.30
more
amine N-hydroxylase cannot carry out the reduction of the flavin cofactor. Rather, the reduced flavin is supplied by a separate flavin reductase. The mechanism for the hydroxylation is likely to proceed via the formation of a flavin 4a-hydroperoxide
Streptomyces viridifaciens MG456-hF10
?
-
?
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