Phosphatidyl-N-methylethanolamine N-methyltransferase
Phosphatidylethanolamine N-methyltransferase
31983
ChemSpider
52924113
PubChem-compound
ReactionCatalysis7386
ACTIVATION
ReactionCatalysis7385
ACTIVATION
4573168
ChemSpider
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
PE-NMe2(14:0/14:1(9Z))
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC
C00350
KEGG Compound
C00157
KEGG Compound
PHOSPHATIDYLCHOLINE
BioCyc
C14H20N6O5S
S-Adenosylhomocysteine
384.12158
5459377
PubChem-compound
C33H64NO8P
PE(14:0/14:1(9Z))
633.43695
PE-NMe(14:0/14:1(9Z))
C00080
KEGG Compound
C34H66NO8P
PE-NMe(14:0/14:1(9Z))
647.4526
L-1-PHOSPHATIDYL-ETHANOLAMINE
BioCyc
SMP0002544
SMPDB
CHEBI:15958
ChEBI
HMDB0001185
HMDB
1.0
P05375
UniProt
P05374
UniProt
CHEBI:15378
ChEBI
SMILES
[H+]
CHEBI:15414
ChEBI
PC(14:0/14:0)
1.0
Phosphatidyl-N-methylethanolamine N-methyltransferase
S-Adenosylmethionine
Phosphatidylethanolamine N-methyltransferase
HMDB0000939
HMDB
SMILES
[H]C(COC(=O)CCCCCCCCCCCCC)(COP(O)(=O)OCCN(C)C)OC(=O)CCCCCCC\C=C/CCCC
C01241
KEGG Compound
Phosphatidylcholine Biosynthesis PC(14:0/14:1(9Z))
Reaction189458
false
PE-NMe2(14:0/14:1(9Z)) + S-Adenosylmethionine → Hydrogen Ion + PC(14:0/14:0) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
HMDB0008822
HMDB
C00019
KEGG Compound
C15H23N6O5S
S-Adenosylmethionine
399.14505
4932
TAXONOMY
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
C36H72NO8P
PC(14:0/14:0)
677.4996
HMDB0112937
HMDB
CHEBI:52332
ChEBI
1.0
2.1.1.17
false
2.1.1.17
PE(14:0/14:1(9Z)) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe(14:0/14:1(9Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
25246222
PubChem-compound
1.0
2.1.1.17,2.1.1.71
false
2.1.1.17,2.1.1.71
PE-NMe(14:0/14:1(9Z)) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe2(14:0/14:1(9Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
HMDB0007866
HMDB
CHEBI:45240
ChEBI
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCC)(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/CCCC
SMILES
[H]C(COC(=O)CCCCCCCCCCCCC)(COP(O)(=O)OCCNC)OC(=O)CCCCCCC\C=C/CCCC
PE(14:0/14:1(9Z))
PW002814
PathWhiz
CPD-405
BioCyc
H
Hydrogen Ion
1.007825
388301
ChemSpider
S-Adenosylhomocysteine
ADENOSYL-HOMO-CYS
BioCyc
C04308
KEGG Compound
HMDB0059597
HMDB
24768328
ChemSpider
485-80-3
CAS
C00021
KEGG Compound
CHEBI:16680
ChEBI
1.0
C35H68NO8P
PE-NMe2(14:0/14:1(9Z))
661.46826
1010
ChemSpider
HMDB0113839
HMDB
CPD-160
BioCyc
24762165
PubChem-compound
Saccharomyces cerevisiae
1.0
1.0