(RS)-1-benzyl-1,2,3,4-tetrahydroisoquinoline N-methyltransferase EC#: 2.1.1.115; 凯望编码 (ChemWhat Code): 1376302

英文名 (RS)-1-benzyl-1,2,3,4-tetrahydroisoquinoline N-methyltransferase
Example Structure Example Structure of (RS)-1-benzyl-1,2,3,4-tetrahydroisoquinoline N-methyltransferase EC#: 2.1.1.115
别名 (R,S)-Tetrahydrobenzylisoquinoline-N-methyltransferase, Methyltransferase, tetrahydrobenzylisoquinoline, NMT, Norreticuline N-methyltransferase
EC Number 2.1.1.115
CAS编号 132084-82-3
Comments 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. The enzyme participates in the pathway leading to benzylisoquinoline alkaloid synthesis in plants. The physiological substrate is likely to be coclaurine. The enzyme 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.
Cofactor
History
Reactions S-adenosyl-L-methionine + (RS)-1-benzyl-1,2,3,4-tetrahydroisoquinoline = S-adenosyl-L-homocysteine + N-methyl-(RS)-1-benzyl-1,2,3,4- tetrahydroisoquinoline.

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