KEGG   ORTHOLOGY: K13386
Entry
K13386                      KO                                     
Symbol
E2.1.1.116
Name
3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase [EC:2.1.1.116]
Pathway
map00950  Isoquinoline alkaloid biosynthesis
map01100  Metabolic pathways
map01110  Biosynthesis of secondary metabolites
Module
M00943  Reticuline biosynthesis, dopamine + 4HPAA => (S)-reticuline
Reaction
R03832  S-adenosyl-L-methionine:3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase
R05212  S-adenosyl-L-methionine:3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase
Brite
KEGG Orthology (KO) [BR:ko00001]
 09100 Metabolism
  09110 Biosynthesis of other secondary metabolites
   00950 Isoquinoline alkaloid biosynthesis
    K13386  E2.1.1.116; 3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase
Enzymes [BR:ko01000]
 2. Transferases
  2.1  Transferring one-carbon groups
   2.1.1  Methyltransferases
    2.1.1.116  3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase
     K13386  E2.1.1.116; 3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase
Other DBs
GO: 0030784
Genes
MING: 122065299 122065307
PSOM: 113294323 113326743 113326977 113327792 113328438 113339850 113339870 113353561
MSIN: 131239723
AG: BAB08005
Reference
  Authors
Morishige T, Tsujita T, Yamada Y, Sato F
  Title
Molecular characterization of the S-adenosyl-L-methionine:3'-hydroxy-N-methylcoclaurine 4'-O-methyltransferase involved in isoquinoline alkaloid biosynthesis in Coptis japonica.
  Journal
J Biol Chem 275:23398-405 (2000)
DOI:10.1074/jbc.M002439200
  Sequence

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