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ENZYME

ENZYME entry: EC 2.1.1.115

Accepted Name
(RS)-1-benzyl-1,2,3,4-tetrahydroisoquinoline N-methyltransferase
Alternative Name(s)
(RS)-tetrahydrobenzylisoquinoline N-methyltransferase
norreticuline N-methyltransferase
Reaction catalysed
(RS)-1-benzyl-1,2,3,4-tetrahydroisoquinoline + S-adenosyl-L-methionine <=> H(+) + N-methyl-(RS)-1-benzyl-1,2,3,4-tetrahydroisoquinoline + S-adenosyl-L-homocysteine
Comment(s)
  • Broad substrate specificity for (RS)-1-benzyl-1,2,3,4- tetrahydroisoquinolines; including coclaurine, norcoclaurine, isococlaurine, norarmepavine, norreticuline and tetrahydropapaverine.
  • Both R- and S-enantiomers are methylated.
  • Participates in the pathway leading to benzylisoquinoline alkaloid synthesis in plants.
  • The physiological substrate is likely to be coclaurine.
  • Was earlier termed norreticuline N-methyltransferase.
  • However, norreticuline has not been found to occur in nature and that name does not reflect the broad specificity of the enzyme for (RS)-1- benzyl-1,2,3,4-tetrahydroisoquinolines.
Cross-references
BRENDA2.1.1.115
EC2PDB2.1.1.115
ExplorEnz2.1.1.115
PRIAM enzyme-specific profiles2.1.1.115
KEGG Ligand Database for Enzyme Nomenclature2.1.1.115
IUBMB Enzyme Nomenclature2.1.1.115
IntEnz2.1.1.115
MEDLINEFind literature relating to 2.1.1.115
MetaCyc2.1.1.115
Rhea expert-curated reactions2.1.1.115

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All ENZYME / UniProtKB/Swiss-Prot entries corresponding to 2.1.1.-
All ENZYME / UniProtKB/Swiss-Prot entries corresponding to 2.1.-.-
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