Phosphatidyl-N-methylethanolamine N-methyltransferase
Phosphatidylethanolamine N-methyltransferase
31983
ChemSpider
ReactionCatalysis7386
ACTIVATION
CHEBI:72999
ChEBI
ReactionCatalysis7385
ACTIVATION
ReactionCatalysis7384
ACTIVATION
Hydrogen Ion
1.0
CHEBI:73007
ChEBI
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
PE(16:0/18:1(9Z))
C00157
KEGG Compound
C14H20N6O5S
S-Adenosylhomocysteine
384.12158
C41H80NO8P
PE-NMe2(16:0/18:1(9Z))
745.56213
C40H78NO8P
PE-NMe(16:0/18:1(9Z))
731.5465
C00080
KEGG Compound
398235
ChemSpider
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCCCC)(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/CCCCCCCC
L-1-PHOSPHATIDYL-ETHANOLAMINE
BioCyc
HMDB0010569
HMDB
CHEBI:15958
ChEBI
4446615
ChemSpider
HMDB0001185
HMDB
1.0
PW002914
PathWhiz
P05375
UniProt
P05374
UniProt
CHEBI:15378
ChEBI
SMILES
[H+]
CHEBI:15414
ChEBI
Phosphatidyl-N-methylethanolamine N-methyltransferase
S-Adenosylmethionine
Phosphatidylethanolamine N-methyltransferase
9547033
PubChem-compound
HMDB0000939
HMDB
C01241
KEGG Compound
2.1.1.17,2.1.1.71
false
2.1.1.17,2.1.1.71
PE-NMe(16:0/18:1(9Z)) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe2(16:0/18:1(9Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
PC(16:0/16:0)
2.1.1.17
false
2.1.1.17
PE(16:0/18:1(9Z)) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe(16:0/18:1(9Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
C40H80NO8P
PC(16:0/16:0)
733.56213
1.0
7825983
ChemSpider
C00019
KEGG Compound
C15H23N6O5S
S-Adenosylmethionine
399.14505
4932
TAXONOMY
452110
PubChem-compound
5283496
PubChem-compound
S-ADENOSYLMETHIONINE
BioCyc
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
CHEBI:52332
ChEBI
25246222
PubChem-compound
PE-NMe(16:0/18:1(9Z))
1.0
SMILES
[H]C(COC(=O)CCCCCCCCCCCCCCC)(COP(O)(=O)OCCN(C)C)OC(=O)CCCCCCC\C=C/CCCCCCCC
PE-NMe2(16:0/18:1(9Z))
C39H76NO8P
PE(16:0/18:1(9Z))
717.5309
SMILES
[H]C(COC(=O)CCCCCCCCCCCCCCC)(COP(O)(=O)OCCNC)OC(=O)CCCCCCC\C=C/CCCCCCCC
Reaction189647
false
PE-NMe2(16:0/18:1(9Z)) + S-Adenosylmethionine → Hydrogen Ion + PC(16:0/16:0) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
SMP0002644
SMPDB
63-89-8
CAS
CPD-405
BioCyc
H
Hydrogen Ion
1.007825
388301
ChemSpider
S-Adenosylhomocysteine
ADENOSYL-HOMO-CYS
BioCyc
C04308
KEGG Compound
9547018
PubChem-compound
HMDB0059597
HMDB
7825968
ChemSpider
485-80-3
CAS
HMDB0010568
HMDB
C00021
KEGG Compound
CHEBI:16680
ChEBI
1010
ChemSpider
PHOSPHATIDYLCHOLINE
BioCyc
CPD-160
BioCyc
1.0
HMDB0008927
HMDB
24762165
PubChem-compound
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCC
Saccharomyces cerevisiae
Phosphatidylcholine Biosynthesis PC(16:0/18:1(9Z))
1.0
HMDB0000564
HMDB
1.0