6022
PubChem-compound
2.1.1.71
false
2.1.1.71
PE-NMe(14:1(9Z)/22:2(13Z,16Z)) + S-Adenosylmethionine → PE-NMe2(14:1(9Z)/22:2(13Z,16Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
C2H8NO4P
O-Phosphoethanolamine
141.01909
PHOSPHORYL-ETHANOLAMINE
BioCyc
Reaction50231
false
PE(14:1(9Z)/22:2(13Z,16Z)) + S-Adenosylmethionine → PE-NMe(14:1(9Z)/22:2(13Z,16Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
Reaction50230
false
PS(14:1(9Z)/22:2(13Z,16Z)) → Carbon dioxide + PE(14:1(9Z)/22:2(13Z,16Z))
LEFT_TO_RIGHT
C02737
KEGG Compound
24766597
ChemSpider
1014
PubChem-compound
1015
PubChem-compound
PE-NMe(14:1(9Z)/22:2(13Z,16Z))
SMILES
[H][C@@](COC(=O)CCCCCCC\C=C/CCCC)(COP(O)(=O)OCCN)OC(=O)CCCCCCCCCCC\C=C/C\C=C/CCCCC
Cytidine triphosphate
L-1-PHOSPHATIDYL-ETHANOLAMINE
BioCyc
HMDB0000095
HMDB
CHEBI:15958
ChEBI
2.1.1.71
false
2.1.1.71
PE-NMe2(14:1(9Z)/22:2(13Z,16Z)) + S-Adenosylmethionine → PC(14:1(9Z)/22:2(13Z,16Z)) + S-Adenosylhomocysteine
LEFT_TO_RIGHT
Pyrophosphate
HMDB0000097
HMDB
HMDB0001185
HMDB
1.0
6131
PubChem-compound
13207
ChemSpider
1.0
HMDB0000538
HMDB
ATP
BioCyc
C01241
KEGG Compound
1.0
559142
ChemSpider
SMILES
CCCCC\C=C/C\C=C/CCCCCCCCCCCC(=O)O[C@]([H])(COC(=O)CCCCCCC\C=C/CCCC)COP([O-])(=O)OCC[N+](C)(C)C
CDP-ETHANOLAMINE
BioCyc
HMDB0007059
HMDB
ADP
BioCyc
110296
ChemSpider
1.0
Choline kinase alpha
ReactionCatalysis40038
ACTIVATION
Choline-phosphate cytidylyltransferase A
ReactionCatalysis40039
ACTIVATION
Choline/ethanolaminephosphotransferase 1
C15H23N6O5S
S-Adenosylmethionine
399.14505
700
PubChem-compound
1.0
1.0
1.0
5742
ChemSpider
6323481
PubChem-compound
C00570
KEGG Compound
1038
PubChem-compound
2.7.7.14
false
2.7.7.14
Cytidine triphosphate + O-Phosphoethanolamine → CDP-ethanolamine + Pyrophosphate
LEFT_TO_RIGHT
274
ChemSpider
ReactionCatalysis40041
ACTIVATION
ReactionCatalysis40042
ACTIVATION
ReactionCatalysis40043
ACTIVATION
ReactionCatalysis40040
ACTIVATION
CPD-405
BioCyc
CHEBI:18303
ChEBI
ADENOSYL-HOMO-CYS
BioCyc
O-Phosphoethanolamine
485-80-3
CAS
C42H78NO8P
PE-NMe(14:1(9Z)/22:2(13Z,16Z))
755.5465
C00588
KEGG Compound
C00346
KEGG Compound
CHEBI:16000
ChEBI
SMP0014267
SMPDB
1010
ChemSpider
PE-NMe2(14:1(9Z)/22:2(13Z,16Z))
C43H80NO8P
PE-NMe2(14:1(9Z)/22:2(13Z,16Z))
769.56213
HMDB0001413
HMDB
PPI
BioCyc
Reaction50229
false
CDP-Choline + DG(14:1(9Z)/22:2(13Z,16Z)/0:0) → Cytidine monophosphate + Hydrogen Ion + PC(14:1(9Z)/22:2(13Z,16Z))
LEFT_TO_RIGHT
Reaction50228
false
CDP-ethanolamine + DG(14:1(9Z)/22:2(13Z,16Z)/0:0) → Cytidine monophosphate + PE(14:1(9Z)/22:2(13Z,16Z))
LEFT_TO_RIGHT
63-37-6
CAS
52922294
PubChem-compound
CHEBI:16732
ChEBI
ReactionCatalysis40019
ACTIVATION
Hydrogen Ion
ReactionCatalysis40015
ACTIVATION
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
C00114
KEGG Compound
PHOSPHATIDYLCHOLINE
BioCyc
1071-23-4
CAS
Adenosine triphosphate
C14H20N6O5S
S-Adenosylhomocysteine
384.12158
Ethanolamine
1.0
124-38-9
CAS
ReactionCatalysis40022
ACTIVATION
CDP-CHOLINE
BioCyc
C00008
KEGG Compound
CHEBI:15414
ChEBI
ReactionCatalysis40025
ACTIVATION
CTP
BioCyc
CHEBI:18361
ChEBI
C00002
KEGG Compound
C39H70O5
DG(14:1(9Z)/22:2(13Z,16Z)/0:0)
618.52234
HMDB0000224
HMDB
13835336
ChemSpider
SMILES
[H][C@](N)(COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCC\C=C/CCCC)OC(=O)CCCCCCCCCCC\C=C/C\C=C/CCCCC)C(O)=O
DG(14:1(9Z)/22:2(13Z,16Z)/0:0)
SMILES
C[N+](C)(C)CCOP([O-])(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(N)=NC1=O
C00019
KEGG Compound
CHEBI:17361
ChEBI
C00011
KEGG Compound
SMILES
O=C=O
S-ADENOSYLMETHIONINE
BioCyc
C00013
KEGG Compound
1.0
CHEBI:52332
ChEBI
HMDB0001564
HMDB
O7P2
Pyrophosphate
173.91193
HMDB0001565
HMDB
1.0
SMILES
C[N+](C)(C)CCOP(O)(O)=O
SMILES
NCCOP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(N)=NC1=O
5957
PubChem-compound
Phosphatidylserine decarboxylase proenzyme
C9H16N3O14P3
Cytidine triphosphate
482.9845
HMDB0008876
HMDB
P35790
UniProt
53477994
PubChem-compound
H
Hydrogen Ion
1.007825
388301
ChemSpider
S-Adenosylhomocysteine
CPD-563
BioCyc
56-65-5
CAS
C00021
KEGG Compound
Cytidine monophosphate
Adenosine diphosphate
HMDB0112315
HMDB
Ethanolamine-phosphate cytidylyltransferase
C10H15N5O10P2
Adenosine diphosphate
427.02942
1.0
1.0
Choline
PHOSPHORYL-CHOLINE
BioCyc
C5H14NO
Choline
104.10754
C9H14N3O8P
Cytidine monophosphate
323.05185
52924154
PubChem-compound
DIACYLGLYCEROL
BioCyc
1.0
P49585
UniProt
C00157
KEGG Compound
24768381
ChemSpider
SMILES
NC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
Q9Y6K0
UniProt
HMDB0000250
HMDB
SMILES
[O-]P([O-])(=O)OP([O-])([O-])=O
14000-31-8
CAS
HMDB0001341
HMDB
Phosphatidylethanolamine N-methyltransferase
2.7.1.82
false
2.7.1.82
Adenosine triphosphate + Ethanolamine → Adenosine diphosphate + Hydrogen Ion + O-Phosphoethanolamine
LEFT_TO_RIGHT
2.7.7.15
false
2.7.7.15
Cytidine triphosphate + Phosphorylcholine → CDP-Choline + Pyrophosphate
LEFT_TO_RIGHT
C00165
KEGG Compound
PE(14:1(9Z)/22:2(13Z,16Z))
Reaction49897
false
Adenosine triphosphate + Choline → Adenosine diphosphate + Phosphorylcholine
LEFT_TO_RIGHT
SMILES
[H]C(COC(=O)CCCCCCC\C=C/CCCC)(COP(O)(=O)OCCNC)OC(=O)CCCCCCCCCCC\C=C/C\C=C/CCCCC
HMDB0000939
HMDB
SMILES
NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
1.0
SMILES
[H]C(COC(=O)CCCCCCC\C=C/CCCC)(COP(O)(=O)OCCN(C)C)OC(=O)CCCCCCCCCCC\C=C/C\C=C/CCCCC
SMILES
C[N+](C)(C)CCO
SMILES
NC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O
1.0
HMDB0000149
HMDB
5901
ChemSpider
CHEBI:15422
ChEBI
Q9UG56
UniProt
305
PubChem-compound
Homo sapiens
CHEBI:18132
ChEBI
C00055
KEGG Compound
SMILES
NCCOP(O)(O)=O
1.0
1.0
C00063
KEGG Compound
ETHANOL-AMINE
BioCyc
C2H7NO
Ethanolamine
61.052765
C10H16N5O13P3
Adenosine triphosphate
506.99576
13628254
ChemSpider
C04308
KEGG Compound
1.0
CHEBI:16526
ChEBI
Phosphatidylserine decarboxylase proenzyme
Q9UBM1
UniProt
CHEBI:16761
ChEBI
C00189
KEGG Compound
107-73-3
CAS
65-47-4
CAS
Ethanolamine-phosphate cytidylyltransferase
1.0
Q99447
UniProt
3036-18-8
CAS
Choline/ethanolaminephosphotransferase 1
987-78-0
CAS
Choline kinase alpha
Choline-phosphate cytidylyltransferase A
9606
TAXONOMY
31983
ChemSpider
5800
ChemSpider
CO2
Carbon dioxide
43.98983
1.0
CMP
BioCyc
C00080
KEGG Compound
SMILES
NCCO
299
ChemSpider
HMDB0007921
HMDB
C11H20N4O11P2
CDP-ethanolamine
446.0604
C5H15NO4P
Phosphorylcholine
184.07387
HMDB0113011
HMDB
CHEBI:17677
ChEBI
6176
PubChem-compound
CHEBI:15378
ChEBI
SMILES
[H+]
L-1-PHOSPHATIDYL-SERINE
BioCyc
58-64-0
CAS
SMILES
NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
CHEBI:17553
ChEBI
S-Adenosylmethionine
123727
PubChem-compound
280
PubChem-compound
PW015138
PathWhiz
11583971
PubChem-compound
Phosphatidylethanolamine N-methyltransferase
644102
PubChem-compound
5941
ChemSpider
CHEBI:16436
ChEBI
C41H76NO8P
PE(14:1(9Z)/22:2(13Z,16Z))
741.5309
Phosphorylcholine
SMILES
N[C@@H](CCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N)C(O)=O
HMDB0113911
HMDB
25246222
PubChem-compound
CDP-ethanolamine
1.0
990
ChemSpider
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/22:2(13Z,16Z))
CHEBI:15354
ChEBI
HMDB0059597
HMDB
C00307
KEGG Compound
141-43-5
CAS
24765893
ChemSpider
Carbon dioxide
HMDB0001967
HMDB
CHEBI:16680
ChEBI
62-49-7
CAS
989
ChemSpider
PS(14:1(9Z)/22:2(13Z,16Z))
CPD-160
BioCyc
24762165
PubChem-compound
PC(14:1(9Z)/22:2(13Z,16Z))
SMILES
[H][C@](CO)(COC(=O)CCCCCCC\C=C/CCCC)OC(=O)CCCCCCCCCCC\C=C/C\C=C/CCCCC
C44H82NO8P
PC(14:1(9Z)/22:2(13Z,16Z))
783.5778
C42H76NO10P
PS(14:1(9Z)/22:2(13Z,16Z))
785.5207
HMDB0000082
HMDB
CDP-Choline
C14H26N4O11P2
CDP-Choline
488.10733