1.5.3.2: N-methyl-L-amino-acid oxidase
This is an abbreviated version!
For detailed information about N-methyl-L-amino-acid oxidase, go to the full flat file.
Word Map on EC 1.5.3.2
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1.5.3.2
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histone
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demethylation
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chromatin
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hydroxylase
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methyltransferase
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aminopyrine
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aniline
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trimethylation
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n6-methyladenosine
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jumonji
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alkbh5
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obesity-associated
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phenobarbital
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h3k4me3
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n-nitrosodimethylamine
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lanosterol
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lysine-specific
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benzoapyrene
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benzphetamine
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nadph-cytochrome
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drug-metabolizing
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azole
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dimethylnitrosamine
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ethylmorphine
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itraconazole
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p-450-dependent
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kabuki
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writer
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p-nitroanisole
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deethylase
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cyp51a
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mixed-function
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o-dealkylase
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nitrosamines
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histone-modifying
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corest
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polycomb
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ten-eleven
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azole-resistant
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epitranscriptomic
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eraser
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fluconazole
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ethoxyresorufin
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mettl14
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lys4
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pentoxyresorufin
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ythdf2
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voriconazole
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3-methylcholanthrene
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7-ethoxycoumarin
- 1.5.3.2
- histone
-
demethylation
- chromatin
- hydroxylase
- methyltransferase
- aminopyrine
- aniline
-
trimethylation
- n6-methyladenosine
-
jumonji
- alkbh5
-
obesity-associated
- phenobarbital
-
h3k4me3
- n-nitrosodimethylamine
- lanosterol
-
lysine-specific
-
benzoapyrene
- benzphetamine
-
nadph-cytochrome
-
drug-metabolizing
- azole
- dimethylnitrosamine
- ethylmorphine
- itraconazole
-
p-450-dependent
-
kabuki
-
writer
-
p-nitroanisole
-
deethylase
- cyp51a
-
mixed-function
-
o-dealkylase
-
nitrosamines
-
histone-modifying
- corest
-
polycomb
-
ten-eleven
-
azole-resistant
-
epitranscriptomic
-
eraser
- fluconazole
-
ethoxyresorufin
- mettl14
- lys4
-
pentoxyresorufin
- ythdf2
- voriconazole
- 3-methylcholanthrene
- 7-ethoxycoumarin
Reaction
Synonyms
demethylase, N-methylamino acid oxidase, oxidase, N-methylamino acid
ECTree
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Substrates Products
Substrates Products on EC 1.5.3.2 - N-methyl-L-amino-acid oxidase
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REACTION DIAGRAM
alpha-N-methyl-L-histidine + O2 + H2O
L-histidine + formaldehyde + H2O2
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?
alpha-N-methyl-L-tryptophan + O2 + H2O
L-tryptophan + formaldehyde + H2O2
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alpha-N-methyl-L-tryptophan is identical with L-abrine
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?
N-methyl-L-amino acid + O2 + H2O
L-amino acid + formaldehyde + H2O2
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enzyme requires the presence of a free alpha-carboxyl group in the substrate molecule, substrates with aromatic or heterocyclic substituents are more readily oxidized, followed by aliphatic N-methylamino acids with long side chain, more slowly activity towards N-methyl derivatives of beta-hydroxy-amino acids and of basic and acidic amino acids with exception of histidin, very slow demethylation of phenylsarcosine
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?
N-methyl-L-norleucine + O2 + H2O
L-norleucine + formaldehyde + H2O2
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-
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?
N-methyl-L-phenylalanine + O2 + H2O
L-phenylalanine + formaldehyde + H2O2
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-
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?
N-methyl-L-tyrosine + O2 + H2O
L-tyrosine + formaldehyde + H2O2
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N-methyl-DL-tyrosine is identical with surinamine
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-
?
N-methyldihydroxyphenyl-DL-alanine + O2 + H2O
formaldehyde + dihydroxyphenyl-DL-alanine + H2O2
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?
additional information
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more substrates, not with: N-dimethyl-L-amino acid, N-methyl-D-amino acid, L-amino acid, D-amino acid
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?