Phosphatidyl-N-methylethanolamine N-methyltransferase
Phosphatidylethanolamine N-methyltransferase
31983
ChemSpider
SMILES
[H]C(COC(=O)CCCCCCCCCCCCCCCCC)(COP(O)(=O)OCCNC)OC(=O)CCCCCCCCCCCCCCCCC
ReactionCatalysis7386
ACTIVATION
ReactionCatalysis7385
ACTIVATION
PW002960
PathWhiz
ReactionCatalysis7384
ACTIVATION
Hydrogen Ion
85004
ChemSpider
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
CHEBI:39934
ChEBI
C00350
KEGG Compound
C00157
KEGG Compound
PHOSPHATIDYLCHOLINE
BioCyc
C14H20N6O5S
S-Adenosylhomocysteine
384.12158
C00080
KEGG Compound
394271
ChemSpider
SMILES
[H]C(COC(=O)CCCCCCCCCCCCCCCCC)(COP(O)(=O)OCCN(C)C)OC(=O)CCCCCCCCCCCCCCCCC
L-1-PHOSPHATIDYL-ETHANOLAMINE
BioCyc
Phosphatidylcholine Biosynthesis PC(18:0/18:0)
CHEBI:15958
ChEBI
94190
PubChem-compound
2.1.1.17,2.1.1.71
false
2.1.1.17,2.1.1.71
PE-NMe(18:0/18:0) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe2(18:0/18:0) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
1.0
2.1.1.17
false
2.1.1.17
PE(18:0/18:0) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe(18:0/18:0) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
HMDB0001185
HMDB
1.0
Reaction7556
false
PE-NMe2(18:0/18:0) + S-Adenosylmethionine → Hydrogen Ion + PC(18:0/18:0) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
1.0
P05375
UniProt
P05374
UniProt
CHEBI:15378
ChEBI
SMILES
[H+]
1.0
CHEBI:15414
ChEBI
1.0
447078
PubChem-compound
Phosphatidyl-N-methylethanolamine N-methyltransferase
S-Adenosylmethionine
Phosphatidylethanolamine N-methyltransferase
HMDB0000939
HMDB
C01241
KEGG Compound
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCCCCCC)(COP(O)(=O)OCCN)OC(=O)CCCCCCCCCCCCCCCCC
HMDB0112975
HMDB
CHEBI:83718
ChEBI
PC(18:0/18:0)
C44H88NO8P
PC(18:0/18:0)
789.62476
C00019
KEGG Compound
C15H23N6O5S
S-Adenosylmethionine
399.14505
4932
TAXONOMY
S-ADENOSYLMETHIONINE
BioCyc
C42H84NO8P
PE-NMe(18:0/18:0)
761.59344
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
1.0
816-94-4
CAS
C43H86NO8P
PE-NMe2(18:0/18:0)
775.60913
HMDB0113876
HMDB
HMDB0008991
HMDB
PE-NMe2(18:0/18:0)
HMDB0008036
HMDB
CPD-405
BioCyc
H
Hydrogen Ion
1.007825
388301
ChemSpider
S-Adenosylhomocysteine
ADENOSYL-HOMO-CYS
BioCyc
C04308
KEGG Compound
HMDB0059597
HMDB
1069-79-0
CAS
485-80-3
CAS
C00021
KEGG Compound
CHEBI:16680
ChEBI
PE-NMe(18:0/18:0)
1010
ChemSpider
CPD-160
BioCyc
24762165
PubChem-compound
SMP0002690
SMPDB
Saccharomyces cerevisiae
PE(18:0/18:0)
1.0
C41H82NO8P
PE(18:0/18:0)
747.5778
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCCCC