1.0
DIACYLGLYCEROL
BioCyc
1.0
C00154
KEGG Compound
Reaction56051
false
PA(18:0/16:0) + Water → DG(18:0/16:0/0:0) + Phosphate
LEFT_TO_RIGHT
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
3246945
PubChem-compound
CPD-8587
BioCyc
439162
PubChem-compound
Reaction56050
false
LPA(18:0/0:0) + Palmityl-CoA → Coenzyme A + PA(18:0/16:0)
LEFT_TO_RIGHT
DG(18:0/16:0/0:0)
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
P21695
UniProt
439153
PubChem-compound
SMILES
O
STEAROYL-COA
BioCyc
545567
PubChem-compound
1.0
474863
ChemSpider
CO-A
BioCyc
NAD
C00165
KEGG Compound
C00681
KEGG Compound
648
ChemSpider
SMP0018287
SMPDB
388366
ChemSpider
SMILES
[H][C@](CO)(COC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC
Coenzyme A
Dihydroxyacetone phosphate
Phosphatidate phosphatase LPIN1
HMDB0001114
HMDB
C21H36N7O16P3S
Coenzyme A
767.11523
SMILES
CCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)C(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
6816
PubChem-compound
C3H7O6P
Dihydroxyacetone phosphate
169.99803
1.0
Glycolysis
SubPathway
Reaction55814
false
Dihydroxyacetone phosphate + Hydrogen Ion + NADH → Glycerol 3-phosphate + NAD
LEFT_TO_RIGHT
CHEBI:15846
ChEBI
HMDB0007854
HMDB
Diacylglycerol O-acyltransferase 1
PALMITYL-COA
BioCyc
HMDB0001473
HMDB
CHEBI:15541
ChEBI
14902
ChemSpider
6557
ChemSpider
668
PubChem-compound
Homo sapiens
1038
PubChem-compound
388299
ChemSpider
7732-18-5
CAS
2190-24-1
CAS
HMDB0001487
HMDB
GO:0005829
GENE ONTOLOGY
1.0
TG(18:0/16:0/18:0)
CHEBI:16908
ChEBI
Reaction55875
false
Glycerol 3-phosphate + Stearoyl-CoA → Coenzyme A + LPA(18:0/0:0)
LEFT_TO_RIGHT
DIHYDROXY-ACETONE-PHOSPHATE
BioCyc
1.0
1-Acyl-sn-glycerol-3-phosphate acyltransferase alpha
O4P
Phosphate
94.95342
1.0
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
OCC(=O)COP(O)(O)=O
O75907
UniProt
ACYL-SN-GLYCEROL-3P
BioCyc
9606
TAXONOMY
962
PubChem-compound
PW019162
PathWhiz
ReactionCatalysis45943
ACTIVATION
CHEBI:16337
ChEBI
Hydrogen Ion
ReactionCatalysis45941
ACTIVATION
1.0
1.0
CHEBI:15525
ChEBI
ReactionCatalysis45942
ACTIVATION
PW000146
PathWhiz
C00111
KEGG Compound
Cytosol
2.0
CHEBI:74850
ChEBI
Phosphate
5893
PubChem-compound
1.0
58-68-4
CAS
C00080
KEGG Compound
Glycerol-3-phosphate acyltransferase 1, mitochondrial
SMP0000040
SMPDB
HMDB0001423
HMDB
SMILES
[O-]P([O-])([O-])=O
Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic
C39H70N7O17P3S
Stearoyl-CoA
1033.3762
HMDB0002111
HMDB
C55H106O6
TG(18:0/16:0/18:0)
862.79895
CHEBI:15377
ChEBI
C00009
KEGG Compound
CHEBI:15378
ChEBI
SMILES
[H+]
14265-44-2
CAS
CHEBI:16108
ChEBI
17989-41-2
CAS
Q14693
UniProt
C00001
KEGG Compound
HMDB0001429
HMDB
De Novo Triacylglycerol Biosynthesis TG(18:0/16:0/18:0)
1763-10-6
CAS
Diacylglycerol O-acyltransferase 1
C00004
KEGG Compound
CHEBI:18367
ChEBI
C00003
KEGG Compound
C21H43O7P
LPA(18:0/0:0)
438.27463
1032
ChemSpider
Q9HCL2
UniProt
Phosphatidate phosphatase LPIN1
C3H9O6P
Glycerol 3-phosphate
172.01367
1.0
GLYCEROL-3P
BioCyc
HMDB0114876
HMDB
Q99943
UniProt
C00093
KEGG Compound
57-04-5
CAS
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCCCCCC)(COP(O)(O)=O)OC(=O)CCCCCCCCCCCCCCC
Glycerol 3-phosphate
HMDB0044722
HMDB
439229
PubChem-compound
C37H73O8P
PA(18:0/16:0)
676.50433
C00416
KEGG Compound
362-66-3
CAS
C21H28N7O14P2
NAD
664.11694
LPA(18:0/0:0)
C00010
KEGG Compound
HMDB0000902
HMDB
C00412
KEGG Compound
1-Acyl-sn-glycerol-3-phosphate acyltransferase alpha
2497483
ChemSpider
L-PHOSPHATIDATE
BioCyc
Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic
7826122
ChemSpider
SMILES
CCCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC
C21H29N7O14P2
NADH
665.12476
Stearoyl-CoA
H2O
Water
18.010565
SMILES
CCCCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)C(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
CHEBI:15978
ChEBI
NADH
BioCyc
NAD
BioCyc
9547179
PubChem-compound
15667
PubChem-compound
H
Hydrogen Ion
1.007825
1061
PubChem-compound
1.0
1.0
HMDB0059597
HMDB
388308
ChemSpider
1.0
Reaction58542
false
DG(18:0/16:0/0:0) + Stearoyl-CoA → Coenzyme A + TG(18:0/16:0/18:0)
LEFT_TO_RIGHT
SMILES
CCCCCCCCCCCCCCCCCC(=O)OCC(O)COP(O)(O)=O
53-84-9
CAS
C37H72O5
DG(18:0/16:0/0:0)
596.53796
ReactionCatalysis45939
ACTIVATION
C37H66N7O17P3S
Palmityl-CoA
1005.34485
SubPathwayInteraction9837
SubPathwayReaction
SubPathway9837Reaction
HMDB0000126
HMDB
Palmityl-CoA
HMDB0001338
HMDB
ReactionCatalysis45940
ACTIVATION
85-61-0
CAS
HMDB0007156
HMDB
SMILES
OC[C@@H](O)COP(O)(O)=O
PA(18:0/16:0)