Triacylglycerols
BioCyc
DIACYLGLYCEROL
BioCyc
1.0
3082227
PubChem-compound
937
ChemSpider
SMILES
NC(=O)C1=C[N+](=CC=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O
CPD-8587
BioCyc
439162
PubChem-compound
17220835
ChemSpider
SubPathwayInteraction27506
SubPathwayReaction
SubPathway27506Reaction
LPA(20:3(8Z,11Z,14Z)/0:0)
5682
ChemSpider
SMILES
NC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](CO[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C(N)N=CN=C23)[C@@H](O)[C@H]1O
Glycerol-3-phosphate acyltransferase 1, mitochondrial
Dihydroxyacetone phosphate
SubPathwayOutput
Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic
NADH
CHEBI:1146900
ChEBI
Water
HMDB0006519
HMDB
P21695
UniProt
439153
PubChem-compound
SMILES
O
28879-98-3
CAS
1.0
PW036144
PathWhiz
52922020
PubChem-compound
De Novo Triacylglycerol Biosynthesis TG(20:3(8Z,11Z,14Z)/24:0/18:4(6Z,9Z,12Z,15Z))
1.0
SMILES
[H][C@@](COC(=O)CCCCCC\C=C/C\C=C/C\C=C/CCCCC)(COP(O)(O)=O)OC(=O)CCCCCCCCCCCCCCCCCCCCCCC
CO-A
BioCyc
NAD
1.0
C00165
KEGG Compound
SMP0035242
SMPDB
C00681
KEGG Compound
648
ChemSpider
Coenzyme A
C47H86O5
DG(20:3(8Z,11Z,14Z)/24:0/0:0)
730.6475
Dihydroxyacetone phosphate
Phosphatidate phosphatase LPIN1
C21H36N7O16P3S
Coenzyme A
767.11523
6816
PubChem-compound
C3H7O6P
Dihydroxyacetone phosphate
169.99803
Glycolysis
SubPathway
HMDB0006526
HMDB
DG(20:3(8Z,11Z,14Z)/24:0/0:0)
Reaction55814
false
Dihydroxyacetone phosphate + Hydrogen Ion + NADH → Glycerol 3-phosphate + NAD
LEFT_TO_RIGHT
CHEBI:15846
ChEBI
Diacylglycerol O-acyltransferase 1
52922033
PubChem-compound
HMDB0001473
HMDB
Reaction79433
false
LPA(20:3(8Z,11Z,14Z)/0:0) + Tetracosanoyl-CoA → Coenzyme A + PA(20:3(8Z,11Z,14Z)/24:0)
LEFT_TO_RIGHT
PA(20:3(8Z,11Z,14Z)/24:0)
Reaction79436
false
DG(20:3(8Z,11Z,14Z)/24:0/0:0) + Stearidonoyl-CoA → Coenzyme A + TG(20:3(8Z,11Z,14Z)/24:0/18:4(6Z,9Z,12Z,15Z))
LEFT_TO_RIGHT
6557
ChemSpider
668
PubChem-compound
Reaction79434
false
PA(20:3(8Z,11Z,14Z)/24:0) + Water → DG(20:3(8Z,11Z,14Z)/24:0/0:0) + Phosphate
LEFT_TO_RIGHT
Homo sapiens
C39H62N7O17P3S
Stearidonoyl-CoA
1025.3136
1038
PubChem-compound
388299
ChemSpider
7732-18-5
CAS
HMDB0001487
HMDB
GO:0005829
GENE ONTOLOGY
1.0
C45H82N7O17P3S
Tetracosanoyl-CoA
1117.4701
C47H87O8P
PA(20:3(8Z,11Z,14Z)/24:0)
810.61383
CHEBI:16908
ChEBI
1.0
DIHYDROXY-ACETONE-PHOSPHATE
BioCyc
1.0
1-Acyl-sn-glycerol-3-phosphate acyltransferase alpha
O4P
Phosphate
94.95342
HMDB0003947
HMDB
1.0
SMILES
CCCCC\C=C/C\C=C/C\C=C/CCCCCCC(=O)OCC(O)COP(O)(O)=O
1010
ChemSpider
SMILES
CC(C)(COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N)[C@@H](O)C(=O)NCCC(=O)NCCS
SMILES
[H][C@](CO)(COC(=O)CCCCCC\C=C/C\C=C/C\C=C/CCCCC)OC(=O)CCCCCCCCCCCCCCCCCCCCCCC
SMILES
OCC(=O)COP(O)(O)=O
O75907
UniProt
HMDB0115585
HMDB
ACYL-SN-GLYCEROL-3P
BioCyc
CHEBI:63545
ChEBI
C16529
KEGG Compound
9606
TAXONOMY
962
PubChem-compound
ReactionCatalysis45943
ACTIVATION
CHEBI:16975
ChEBI
CHEBI:16337
ChEBI
Hydrogen Ion
ReactionCatalysis45941
ACTIVATION
ReactionCatalysis45942
ACTIVATION
PW000146
PathWhiz
C00111
KEGG Compound
Cytosol
SMILES
CC\C=C/C\C=C/C\C=C/C\C=C/CCCCC(=O)SCCNC(=O)CCNC(=O)[C@@](O)([H])C(C)(C)COP(=O)(O)OP(=O)(O)OC[C@H]1O[C@H](C(O)[C@H]1OP(=O)(O)O)N1C=NC2=C1N=CN=C2N
2.0
Phosphate
5893
PubChem-compound
1.0
58-68-4
CAS
C00080
KEGG Compound
Glycerol-3-phosphate acyltransferase 1, mitochondrial
Tetracosanoyl-CoA
SMP0000040
SMPDB
C41H68N7O17P3S
Dihomo-γ-Linolenoyl-CoA
1055.3605
HMDB0001423
HMDB
C23H41O7P
LPA(20:3(8Z,11Z,14Z)/0:0)
460.259
SMILES
[O-]P([O-])([O-])=O
Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic
SMILES
[H][C@](O)(C(=O)NCCC(=O)NCCSC(=O)CCCCCCCCCCCCCCCCCCCCCCC)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@@H](O)C1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
HMDB0002111
HMDB
CHEBI:15377
ChEBI
C00009
KEGG Compound
CHEBI:15378
ChEBI
SMILES
[H+]
14265-44-2
CAS
1.0
CHEBI:16108
ChEBI
17989-41-2
CAS
Q14693
UniProt
CHEBI:27979
ChEBI
C00001
KEGG Compound
HMDB0001429
HMDB
Diacylglycerol O-acyltransferase 1
C00004
KEGG Compound
CHEBI:18367
ChEBI
C00003
KEGG Compound
1.0
1032
ChemSpider
Stearidonoyl-CoA
Q9HCL2
UniProt
HMDB0114759
HMDB
Phosphatidate phosphatase LPIN1
C3H9O6P
Glycerol 3-phosphate
172.01367
1.0
GLYCEROL-3P
BioCyc
Q99943
UniProt
C00093
KEGG Compound
HMDB0007499
HMDB
57-04-5
CAS
Glycerol 3-phosphate
SMILES
[H][C@](COC(=O)CCCCCC\C=C/C\C=C/C\C=C/CCCCC)(COC(=O)CCCC\C=C/C\C=C/C\C=C/C\C=C/CC)OC(=O)CCCCCCCCCCCCCCCCCCCCCCC
C00416
KEGG Compound
1.0
C21H28N7O14P2
NAD
664.11694
C16163
KEGG Compound
C00010
KEGG Compound
HMDB0000902
HMDB
1-Acyl-sn-glycerol-3-phosphate acyltransferase alpha
24305-30-4
CAS
L-PHOSPHATIDATE
BioCyc
Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic
C21H29N7O14P2
NADH
665.12476
SMILES
CCCCC\C=C/C\C=C/C\C=C/CCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
H2O
Water
18.010565
Reaction71354
false
Dihomo-γ-Linolenoyl-CoA + Glycerol 3-phosphate → Coenzyme A + LPA(20:3(8Z,11Z,14Z)/0:0)
LEFT_TO_RIGHT
Dihomo-γ-Linolenoyl-CoA
CHEBI:15978
ChEBI
NADH
BioCyc
NAD
BioCyc
H
Hydrogen Ion
1.007825
1061
PubChem-compound
HMDB0059597
HMDB
388308
ChemSpider
1.0
53478285
PubChem-compound
53-84-9
CAS
C00422
KEGG Compound
ReactionCatalysis45939
ACTIVATION
24766193
ChemSpider
1.0
CHEBI:52974
ChEBI
HMDB0000126
HMDB
ReactionCatalysis45940
ACTIVATION
85-61-0
CAS
TG(20:3(8Z,11Z,14Z)/24:0/18:4(6Z,9Z,12Z,15Z))
C65H112O6
TG(20:3(8Z,11Z,14Z)/24:0/18:4(6Z,9Z,12Z,15Z))
988.8459
SMILES
OC[C@@H](O)COP(O)(O)=O