Phosphatidyl-N-methylethanolamine N-methyltransferase
Phosphatidylethanolamine N-methyltransferase
31983
ChemSpider
1.0
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
C42H80NO8P
PE-NMe(18:1(9Z)/18:1(11Z))
757.56213
C00157
KEGG Compound
PHOSPHATIDYLCHOLINE
BioCyc
C14H20N6O5S
S-Adenosylhomocysteine
384.12158
6437081
PubChem-compound
SMILES
[H][C@@](COC(=O)CCCCCCC\C=C/CCCCCCCC)(COP(O)(=O)OCCN)OC(=O)CCCCCCCCC\C=C/CCCCCC
C00080
KEGG Compound
PE(18:1(9Z)/18:1(11Z))
HMDB0112967
HMDB
L-1-PHOSPHATIDYL-ETHANOLAMINE
BioCyc
Reaction189700
false
PE-NMe2(18:1(9Z)/18:1(11Z)) + S-Adenosylmethionine → Hydrogen Ion + PC(18:1(9Z)/18:1(9Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
CHEBI:15958
ChEBI
HMDB0001185
HMDB
1.0
P05375
UniProt
P05374
UniProt
4941669
ChemSpider
CHEBI:15378
ChEBI
SMILES
[H+]
CHEBI:15414
ChEBI
PE-NMe(18:1(9Z)/18:1(11Z))
Phosphatidyl-N-methylethanolamine N-methyltransferase
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(18:1(9Z)/18:1(11Z)) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe2(18:1(9Z)/18:1(11Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
C43H82NO8P
PE-NMe2(18:1(9Z)/18:1(11Z))
771.5778
SMILES
CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/CCCCCCCC
HMDB0113868
HMDB
PE-NMe2(18:1(9Z)/18:1(11Z))
SMP0002672
SMPDB
2.1.1.17
false
2.1.1.17
PE(18:1(9Z)/18:1(11Z)) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe(18:1(9Z)/18:1(11Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
1.0
C00019
KEGG Compound
PW002942
PathWhiz
C15H23N6O5S
S-Adenosylmethionine
399.14505
4932
TAXONOMY
S-ADENOSYLMETHIONINE
BioCyc
1038
PubChem-compound
SMILES
[H]C(COC(=O)CCCCCCC\C=C/CCCCCCCC)(COP(O)(=O)OCCN(C)C)OC(=O)CCCCCCCCC\C=C/CCCCCC
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/CCCCCCCC)(COP(O)(=O)OCCNC)OC(=O)CCCCCCCCC\C=C/CCCCCC
CHEBI:52332
ChEBI
25246222
PubChem-compound
1.0
1.0
C41H78NO8P
PE(18:1(9Z)/18:1(11Z))
743.5465
68737-67-7
CAS
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/18:1(11Z))
HMDB0000593
HMDB
CPD-405
BioCyc
H
Hydrogen Ion
1.007825
388301
ChemSpider
S-Adenosylhomocysteine
ADENOSYL-HOMO-CYS
BioCyc
C04308
KEGG Compound
24768528
ChemSpider
HMDB0059597
HMDB
485-80-3
CAS
C00021
KEGG Compound
CHEBI:16680
ChEBI
53479650
PubChem-compound
1010
ChemSpider
CPD-160
BioCyc
24762165
PubChem-compound
Saccharomyces cerevisiae
1.0
PC(18:1(9Z)/18:1(9Z))
1.0
HMDB0009058
HMDB
C44H84NO8P
PC(18:1(9Z)/18:1(9Z))
785.59344