Any feedback?
Please rate this page
(all_enzymes.php)
(0/150)

BRENDA support

2.1.1.267: flavonoid 3',5'-methyltransferase

This is an abbreviated version!
For detailed information about flavonoid 3',5'-methyltransferase, go to the full flat file.

Word Map on EC 2.1.1.267

Reaction

S-adenosyl-L-methionine
+
a 3'-hydroxyflavonoid
=
S-adenosyl-L-homocysteine
+
a 3'-methoxyflavonoid

Synonyms

3'-OMT, A3'5'OMT, anthocyanin methyltransferase, anthocyanin O-methyltransferase, AnthOMT, AOMT, AOMT1, AOMT2, AOMT3, CdFOMT1, CdFOMT3, CdFOMT4, CdFOMT5, CdFOMT6, CrCOMT2, CrOMT2, EC 2.1.1.149, flavonoid 3',5'-O-dimethyltransferase, flavonoid O-methyltransferase, flavonoid-O-methyltransferase, FOMT1, FOMT3, FOMT4, FOMT5, FOMT6, methyltransferase, flavonoid, Mg2+-independent O-methyltransferase, More, NmAMT6, OMT2, OMT3, PsAOMT, PtAOMT, ROMT-15, ROMT-17, S-adenosylmethionine: anthocyanin 3'5'-methyltransferase, SlOMT3, ThAOMT, TMT5, type II OMT

ECTree

     2 Transferases
         2.1 Transferring one-carbon groups
             2.1.1 Methyltransferases
                2.1.1.267 flavonoid 3',5'-methyltransferase

Natural Substrates Products

Natural Substrates Products on EC 2.1.1.267 - flavonoid 3',5'-methyltransferase

Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
NATURAL SUBSTRATE
NATURAL PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
COMMENTARY
(Substrate) hide
LITERATURE
(Substrate)
COMMENTARY
(Product) hide
LITERATURE
(Product)
REVERSIBILITY
r=reversible
ir=irreversible
?=not specified
4 S-adenosyl-L-methionine + quercetin
4 S-adenosyl-L-homocysteine + 3,3',5,7-tetramethoxyquercetin
show the reaction diagram
whole-cell biocatalysis using CdFOMT5 expressed in Escherichia coli cells is performed using quercetin as a substrate, and 3,3',5,7-tetramethylated quercetin is obtained as the final product
-
-
?
S-adenosyl-L-methionine + 3'-methoxydelphinidin 3-O-glucoside
S-adenosyl-L-homocysteine + 3',5'-dimethoxydelphinidin 3-O-glucoside
show the reaction diagram
very low activity, with delphinidin 3-O-glucoside as substrate, NmAMT6 almost exclusively yields petunidin 3-O-glucoside rather than malvidin 3-O-glucoside. This specificity is consistent with the anthocyanin composition of Nemophila petals
-
-
?
S-adenosyl-L-methionine + a 3'-hydroxyflavonoid
S-adenosyl-L-homocysteine + a 3'-methoxyflavonoid
show the reaction diagram
S-adenosyl-L-methionine + cyanidin 3-O-beta-D-glucoside
S-adenosyl-L-homocysteine + peonidin 3-O-beta-D-glucoside + H+
show the reaction diagram
-
-
-
?
S-adenosyl-L-methionine + delphinidin 3-O-glucoside
S-adenosyl-L-homocysteine + 3'-methoxydelphinidin 3-O-glucoside
show the reaction diagram
S-adenosyl-L-methionine + delphinidin 3-O-glucoside
S-adenosyl-L-homocysteine + petunidin 3-O-beta-D-glucoside
show the reaction diagram
-
-
-
?
S-adenosyl-L-methionine + myricetin
?
show the reaction diagram
involvement in biosynthesis of flavonol glycosides and anthocyanins
-
-
?
S-adenosyl-L-methionine + petunidin 3-O-beta-D-glucoside
S-adenosyl-L-homocysteine + malvidin 3-O-beta-D-glucoside
show the reaction diagram
-
-
-
?
additional information
?
-