Phosphatidyl-N-methylethanolamine N-methyltransferase
Phosphatidylethanolamine N-methyltransferase
31983
ChemSpider
HMDB0008891
HMDB
ReactionCatalysis7386
ACTIVATION
CHEBI:16337
ChEBI
PE(15:0/16:1(9Z))
ReactionCatalysis7385
ACTIVATION
ReactionCatalysis7384
ACTIVATION
Hydrogen Ion
SMILES
C[S+](CC[C@H](N)C(O)=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N
979-92-0
CAS
C00350
KEGG Compound
C37H72NO8P
PE-NMe(15:0/16:1(9Z))
689.4996
C00157
KEGG Compound
PHOSPHATIDYLCHOLINE
BioCyc
C14H20N6O5S
S-Adenosylhomocysteine
384.12158
C38H74NO8P
PE-NMe2(15:0/16:1(9Z))
703.5152
C00080
KEGG Compound
Reaction189544
false
PE-NMe2(15:0/16:1(9Z)) + S-Adenosylmethionine → Hydrogen Ion + PC(15:0/15:0) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
L-1-PHOSPHATIDYL-ETHANOLAMINE
BioCyc
C38H76NO8P
PC(15:0/15:0)
705.5309
CHEBI:15958
ChEBI
2.1.1.17,2.1.1.71
false
2.1.1.17,2.1.1.71
PE-NMe(15:0/16:1(9Z)) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe2(15:0/16:1(9Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
2.1.1.17
false
2.1.1.17
PE(15:0/16:1(9Z)) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe(15:0/16:1(9Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
HMDB0001185
HMDB
1.0
P05375
UniProt
P05374
UniProt
CHEBI:15378
ChEBI
SMILES
[H+]
CHEBI:15414
ChEBI
Phosphatidyl-N-methylethanolamine N-methyltransferase
PE-NMe2(15:0/16:1(9Z))
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCCC)(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/CCCCCC
S-Adenosylmethionine
PE-NMe(15:0/16:1(9Z))
1.0
Phosphatidylethanolamine N-methyltransferase
HMDB0000939
HMDB
24768394
ChemSpider
C01241
KEGG Compound
SMP0002590
SMPDB
HMDB0007934
HMDB
C00019
KEGG Compound
C15H23N6O5S
S-Adenosylmethionine
399.14505
4932
TAXONOMY
PW002860
PathWhiz
52924932
PubChem-compound
S-ADENOSYLMETHIONINE
BioCyc
SMILES
[H]C(COC(=O)CCCCCCCCCCCCCC)(COP(O)(=O)OCCN(C)C)OC(=O)CCCCCCC\C=C/CCCCCC
24766610
ChemSpider
1038
PubChem-compound
SMILES
N[C@@H](CCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N)C(O)=O
SMILES
[H]C(COC(=O)CCCCCCCCCCCCCC)(COP(O)(=O)OCCNC)OC(=O)CCCCCCC\C=C/CCCCCC
CHEBI:52332
ChEBI
25246222
PubChem-compound
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCC
HMDB0112945
HMDB
PC(15:0/15:0)
1.0
1.0
1.0
Phosphatidylcholine Biosynthesis PC(15:0/16:1(9Z))
24778654
PubChem-compound
CPD-405
BioCyc
H
Hydrogen Ion
1.007825
388301
ChemSpider
S-Adenosylhomocysteine
ADENOSYL-HOMO-CYS
BioCyc
C04308
KEGG Compound
HMDB0059597
HMDB
485-80-3
CAS
C00021
KEGG Compound
CHEBI:16680
ChEBI
C36H70NO8P
PE(15:0/16:1(9Z))
675.4839
1010
ChemSpider
CPD-160
BioCyc
24762165
PubChem-compound
Saccharomyces cerevisiae
HMDB0113846
HMDB
1.0
1.0