Phosphatidyl-N-methylethanolamine N-methyltransferase
Phosphatidylethanolamine N-methyltransferase
31983
ChemSpider
ReactionCatalysis7386
ACTIVATION
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
C00157
KEGG Compound
PHOSPHATIDYLCHOLINE
BioCyc
C14H20N6O5S
S-Adenosylhomocysteine
384.12158
C00080
KEGG Compound
L-1-PHOSPHATIDYL-ETHANOLAMINE
BioCyc
SMILES
[H]C(COC(=O)CCCCCCC\C=C/CCCC)(COP(O)(=O)OCCNC)OC(=O)CCCCCCCCCCCCCCCCCCC
HMDB0112960
HMDB
CHEBI:15958
ChEBI
PW002912
PathWhiz
HMDB0001185
HMDB
1.0
P05375
UniProt
P05374
UniProt
CHEBI:15378
ChEBI
SMILES
[H+]
CHEBI:15414
ChEBI
Phosphatidyl-N-methylethanolamine N-methyltransferase
C41H80NO8P
PE-NMe2(14:1(9Z)/20:0)
745.56213
C39H76NO8P
PE(14:1(9Z)/20:0)
717.5309
S-Adenosylmethionine
Phosphatidylethanolamine N-methyltransferase
HMDB0000939
HMDB
C01241
KEGG Compound
2.1.1.17,2.1.1.71
false
2.1.1.17,2.1.1.71
PE-NMe(14:1(9Z)/20:0) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe2(14:1(9Z)/20:0) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
PC(14:1(9Z)/14:1(9Z))
C36H68NO8P
PC(14:1(9Z)/14:1(9Z))
673.46826
1.0
HMDB0008866
HMDB
HMDB0113861
HMDB
1.0
1.0
C00019
KEGG Compound
C15H23N6O5S
S-Adenosylmethionine
399.14505
4932
TAXONOMY
24778648
PubChem-compound
PE(14:1(9Z)/20:0)
S-ADENOSYLMETHIONINE
BioCyc
1038
PubChem-compound
24766576
ChemSpider
SMILES
N[C@@H](CCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N)C(O)=O
PE-NMe2(14:1(9Z)/20:0)
CHEBI:52332
ChEBI
C40H78NO8P
PE-NMe(14:1(9Z)/20:0)
731.5465
2.1.1.17
false
2.1.1.17
PE(14:1(9Z)/20:0) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe(14:1(9Z)/20:0) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
25246222
PubChem-compound
Reaction189644
false
PE-NMe2(14:1(9Z)/20:0) + S-Adenosylmethionine → Hydrogen Ion + PC(14:1(9Z)/14:1(9Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
1.0
HMDB0007900
HMDB
PE-NMe(14:1(9Z)/20:0)
SMP0002642
SMPDB
52924145
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
SMILES
[H]C(COC(=O)CCCCCCC\C=C/CCCC)(COP(O)(=O)OCCN(C)C)OC(=O)CCCCCCCCCCCCCCCCCCC
SMILES
[H][C@@](COC(=O)CCCCCCC\C=C/CCCC)(COP(O)(=O)OCCN)OC(=O)CCCCCCCCCCCCCCCCCCC
1010
ChemSpider
CPD-160
BioCyc
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/20:0)
24762165
PubChem-compound
SMILES
CCCC\C=C/CCCCCCCC(=O)OC[C@]([H])(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/CCCC
Saccharomyces cerevisiae
24768371
ChemSpider
1.0
1.0