Phosphatidyl-N-methylethanolamine N-methyltransferase
Phosphatidylethanolamine N-methyltransferase
31983
ChemSpider
1.0
ReactionCatalysis7386
ACTIVATION
CHEBI:72999
ChEBI
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
C00157
KEGG Compound
C14H20N6O5S
S-Adenosylhomocysteine
384.12158
C00080
KEGG Compound
398235
ChemSpider
L-1-PHOSPHATIDYL-ETHANOLAMINE
BioCyc
HMDB0008933
HMDB
SMILES
[H]C(COC(=O)CCCCCCCCCCCCCCC)(COP(O)(=O)OCCN(C)C)OC(=O)CCCCCCCCC\C=C/CCCCCCCC
CHEBI:15958
ChEBI
HMDB0001185
HMDB
PW002957
PathWhiz
1.0
P05375
UniProt
P05374
UniProt
CHEBI:15378
ChEBI
SMILES
[H+]
CHEBI:15414
ChEBI
Phosphatidyl-N-methylethanolamine N-methyltransferase
S-Adenosylmethionine
Phosphatidylethanolamine N-methyltransferase
HMDB0000939
HMDB
C01241
KEGG Compound
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCCCC)(COP(O)(=O)OCCN)OC(=O)CCCCCCCCC\C=C/CCCCCCCC
PC(16:0/16:0)
HMDB0112973
HMDB
C40H80NO8P
PC(16:0/16:0)
733.56213
C00019
KEGG Compound
C15H23N6O5S
S-Adenosylmethionine
399.14505
4932
TAXONOMY
2.1.1.17
false
2.1.1.17
PE(16:0/20:1(11Z)) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe(16:0/20:1(11Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
452110
PubChem-compound
2.1.1.17,2.1.1.71
false
2.1.1.17,2.1.1.71
PE-NMe(16:0/20:1(11Z)) + S-Adenosylmethionine → Hydrogen Ion + PE-NMe2(16:0/20:1(11Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
S-ADENOSYLMETHIONINE
BioCyc
Reaction189729
false
PE-NMe2(16:0/20:1(11Z)) + S-Adenosylmethionine → Hydrogen Ion + PC(16:0/16:0) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
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
PE-NMe2(16:0/20:1(11Z))
1.0
C42H82NO8P
PE-NMe(16:0/20:1(11Z))
759.5778
25246222
PubChem-compound
1.0
PE-NMe(16:0/20:1(11Z))
HMDB0113874
HMDB
C43H84NO8P
PE-NMe2(16:0/20:1(11Z))
773.59344
SMP0002687
SMPDB
63-89-8
CAS
CPD-405
BioCyc
H
Hydrogen Ion
1.007825
388301
ChemSpider
S-Adenosylhomocysteine
ADENOSYL-HOMO-CYS
BioCyc
C04308
KEGG Compound
HMDB0059597
HMDB
1.0
485-80-3
CAS
C00021
KEGG Compound
CHEBI:16680
ChEBI
SMILES
[H]C(COC(=O)CCCCCCCCCCCCCCC)(COP(O)(=O)OCCNC)OC(=O)CCCCCCCCC\C=C/CCCCCCCC
9547010
PubChem-compound
1010
ChemSpider
PHOSPHATIDYLCHOLINE
BioCyc
CPD-160
BioCyc
1.0
24762165
PubChem-compound
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCC
Phosphatidylcholine Biosynthesis PC(16:0/20:1(11Z))
Saccharomyces cerevisiae
C41H80NO8P
PE(16:0/20:1(11Z))
745.56213
HMDB0000564
HMDB
1.0
PE(16:0/20:1(11Z))
7825960
ChemSpider