KEGG   ENZYME: 2.1.1.128Help
Entry
EC 2.1.1.128                Enzyme                                 

Name (RS)-norcoclaurine 6-O-methyltransferase
Class Transferases;
Transferring one-carbon groups;
Methyltransferases
BRITE hierarchy
Sysname S-adenosyl-L-methionine:(RS)-norcoclaurine 6-O-methyltransferase
Reaction(IUBMB) S-adenosyl-L-methionine + (RS)-norcoclaurine =
S-adenosyl-L-homocysteine + (RS)-coclaurine [RN:R05162]
Reaction(KEGG) R05162 > R05123;
(other) R04715 R05214 R08793
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Substrate S-adenosyl-L-methionine [CPD:C00019];
(R,S)-norcoclaurine [CPD:C06346]
Product S-adenosyl-L-homocysteine [CPD:C00021];
(R,S)-coclaurine [CPD:C06348]
Comment The enzyme will also catalyse the 6-O-methylation of
(RS)-norlaudanosoline to form 6-O-methyl-norlaudanosoline, but this
alkaloid has not been found to occur in plants.
Pathway ec00950  Isoquinoline alkaloid biosynthesis
ec01100  Metabolic pathways
ec01110  Biosynthesis of secondary metabolites
Orthology K13383  (RS)-norcoclaurine 6-O-methyltransferase
Reference
  Authors
  Title


  Journal
1
Rueffer, M., Nagakura, N., Zenk, M.H.
Partial purification and properties of
S-adenosyl-L-methionine:(R),(S)-norlaudanosoline-6-O-methyltransfera
se from Argemone platyceras cell cultures.
Planta Med. 49 (1983) 131-137.
Reference
  Authors
  Title


  Journal
  Organism
2  [PMID:7925429]
Sato F, Tsujita T, Katagiri Y, Yoshida S, Yamada Y.
Purification and characterization of S-adenosyl-L-methionine:
norcoclaurine 6-O-methyltransferase from cultured Coptis japonica
cells.
Eur. J. Biochem. 225 (1994) 125-31.
Coptis japonica
Reference
  Authors
  Title

  Journal
3
Stadler, R., Zenk, M.H.
A revision of the generally accepted pathway for the biosynthesis of
the benzyltetrahydroisoquinoline reticuline.
Liebigs Ann. Chem. (1990) 555-562.
Other DBs ExplorEnz - The Enzyme Database: 2.1.1.128
IUBMB Enzyme Nomenclature: 2.1.1.128
ExPASy - ENZYME nomenclature database: 2.1.1.128
BRENDA, the Enzyme Database: 2.1.1.128
CAS: 89700-33-4

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