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
C41H78NO8P
PE-NMe2(16:1(9Z)/18:1(11Z))
743.5465
C00350
KEGG Compound
HMDB0112957
HMDB
C00157
KEGG Compound
PHOSPHATIDYLCHOLINE
BioCyc
C14H20N6O5S
S-Adenosylhomocysteine
384.12158
24766671
ChemSpider
C00080
KEGG Compound
HMDB0113858
HMDB
Reaction189622
false
PE-NMe2(16:1(9Z)/18:1(11Z)) + S-Adenosylmethionine → Hydrogen Ion + PC(16:1(9Z)/16:1(9Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
C39H74NO8P
PE(16:1(9Z)/18:1(11Z))
715.5152
L-1-PHOSPHATIDYL-ETHANOLAMINE
BioCyc
2.1.1.17,2.1.1.71
false
2.1.1.17,2.1.1.71
PE-NMe(16:1(9Z)/18:1(11Z)) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe2(16:1(9Z)/18:1(11Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
PC(16:1(9Z)/16:1(9Z))
CHEBI:15958
ChEBI
HMDB0001185
HMDB
1.0
SMILES
CCCCCC\C=C/CCCCCCCC(=O)OC[C@]([H])(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/CCCCCC
P05375
UniProt
P05374
UniProt
CHEBI:15378
ChEBI
SMILES
[H+]
CHEBI:15414
ChEBI
Phosphatidyl-N-methylethanolamine N-methyltransferase
PE-NMe2(16:1(9Z)/18:1(11Z))
S-Adenosylmethionine
Phosphatidylethanolamine N-methyltransferase
53479596
PubChem-compound
HMDB0000939
HMDB
C01241
KEGG Compound
2.1.1.17
false
2.1.1.17
PE(16:1(9Z)/18:1(11Z)) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe(16:1(9Z)/18:1(11Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
C40H76NO8P
PE-NMe(16:1(9Z)/18:1(11Z))
729.5309
PE-NMe(16:1(9Z)/18:1(11Z))
1.0
CHEBI:83717
ChEBI
SMP0002632
SMPDB
PW002902
PathWhiz
24778764
PubChem-compound
C00019
KEGG Compound
C15H23N6O5S
S-Adenosylmethionine
399.14505
4932
TAXONOMY
S-ADENOSYLMETHIONINE
BioCyc
1.0
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)CCCCCCC\C=C/CCCCCC)(COP(O)(=O)OCCN(C)C)OC(=O)CCCCCCCCC\C=C/CCCCCC
CHEBI:52332
ChEBI
SMILES
[H][C@@](COC(=O)CCCCCCC\C=C/CCCCCC)(COP(O)(=O)OCCN)OC(=O)CCCCCCCCC\C=C/CCCCCC
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/18:1(11Z))
HMDB0008959
HMDB
25246222
PubChem-compound
PE(16:1(9Z)/18:1(11Z))
1.0
1.0
C40H76NO8P
PC(16:1(9Z)/16:1(9Z))
729.5309
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
24768445
ChemSpider
1010
ChemSpider
CPD-160
BioCyc
24762165
PubChem-compound
Saccharomyces cerevisiae
1.0
SMILES
[H]C(COC(=O)CCCCCCC\C=C/CCCCCC)(COP(O)(=O)OCCNC)OC(=O)CCCCCCCCC\C=C/CCCCCC
1.0
HMDB0008002
HMDB