Compound/PW C003150/Stoichiometry/1.0
type: Stoichiometry
physical entity: DG(16:0/16:1(9Z)/0:0)
stoichiometric coefficient: 1.0

Reference/ChemSpider 937
type: UnificationXref
id: 937
db: ChemSpider

Reference/PubChem-compound 439162
type: UnificationXref
id: 439162
db: PubChem-compound

Transport5937
type: Transport
participant stoichiometry: Compound/PW C003904 Endoplasmic Reticulum Membrane/Stoichiometry/1.0
participant stoichiometry: Compound/PW C003904 Mitochondrial Outer Membrane/Stoichiometry/1.0
right: LPA(16:0/0:0)
spontaneous: false
left: LPA(16:0/0:0)
name: LPA(16:0/0:0) (→) Transport: Caenorhabditis elegans, Cell, Mitochondrial Outer Membrane to Caenorhabditis elegans, Cell, Endoplasmic Reticulum Membrane
conversion direction: LEFT_TO_RIGHT

Reference/PathWhiz PW086762
type: UnificationXref
id: PW086762
db: PathWhiz

NADH
type: SmallMolecule
entity reference: NADH

Reaction141885
type: BiochemicalReaction
participant stoichiometry: Compound/PW C003150/Stoichiometry/1.0
participant stoichiometry: Compound/PW C055586/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001104/Stoichiometry/1.0
right: DG(16:0/16:1(9Z)/0:0)
right: Phosphate
spontaneous: false
left: Water
left: PA(16:0/16:1(9Z))
name: PA(16:0/16:1(9Z)) + Water → DG(16:0/16:1(9Z)/0:0) + Phosphate
conversion direction: LEFT_TO_RIGHT

Reference/ChEBI CHEBI 75354
type: UnificationXref
id: CHEBI:75354
db: ChEBI

Reference/PubChem-compound 439153
type: UnificationXref
id: 439153
db: PubChem-compound

ChemicalStructure/PW C001420
type: ChemicalStructure
structure format: SMILES
structure data: O

Compound/PW C040034/Stoichiometry/1.0
type: Stoichiometry
physical entity: Hydrogen Ion
stoichiometric coefficient: 1.0

Compound/PW C055586/Stoichiometry/1.0
type: Stoichiometry
physical entity: PA(16:0/16:1(9Z))
stoichiometric coefficient: 1.0

De Novo Triacylglycerol Biosynthesis TG(16:0/16:1(9Z)/18:1(11Z))
type: Pathway
pathway order: PathwaySubPathway/78964
pathway order: PathwayTransport/1630254
pathway order: PathwayEnzymeReaction/1630259
pathway order: PathwayEnzymeReaction/1630258
pathway order: PathwayEnzymeReaction/1630257
pathway order: PathwayEnzymeReaction/1630256
pathway order: PathwayEnzymeReaction/1630255
pathway component: Reaction139156
pathway component: Reaction141885
pathway component: ReactionCatalysis128237
pathway component: ReactionCatalysis128236
pathway component: ReactionCatalysis128202
pathway component: ReactionCatalysis128235
pathway component: Reaction141890
pathway component: ReactionCatalysis128234
pathway component: Glycolysis
pathway component: Reaction138125
pathway component: Reaction139269
pathway component: Transport5937
xref: Reference/PathWhiz PW086762
xref: Reference/SMPDB SMP0085743
organism: Caenorhabditis elegans

NAD
type: SmallMolecule
entity reference: NAD

Compound/PW C003904/Stoichiometry/1.0
type: Stoichiometry
physical entity: LPA(16:0/0:0)
stoichiometric coefficient: 1.0

Reference/KEGG Compound C00681
type: UnificationXref
id: C00681
db: KEGG Compound

Dihydroxyacetone phosphate
type: SmallMolecule
entity reference: Dihydroxyacetone phosphate

Reference/PubChem-compound 6816
type: UnificationXref
id: 6816
db: PubChem-compound

PA(16:0/16:1(9Z))
type: SmallMolecule
entity reference: PA(16:0/16:1(9Z))

Dihydroxyacetone phosphate
type: SmallMoleculeReference
xref: Reference/BioCyc DIHYDROXY-ACETONE-PHOSPHATE
xref: Reference/PubChem-compound 668
xref: Reference/ChEBI CHEBI 16108
xref: Reference/KEGG Compound C00111
xref: Reference/CAS 57-04-5
xref: Reference/ChemSpider 648
xref: Reference/HMDB HMDB0001473
chemical formula: C3H7O6P
molecular weight: 169.99803
structure: ChemicalStructure/PW C001134

Reference/ChEBI CHEBI 15846
type: UnificationXref
id: CHEBI:15846
db: ChEBI

Reference/HMDB HMDB0006521
type: UnificationXref
id: HMDB0006521
db: HMDB

Reference/HMDB HMDB0007853
type: UnificationXref
id: HMDB0007853
db: HMDB

Reference/BioCyc PALMITYL-COA
type: UnificationXref
id: PALMITYL-COA
db: BioCyc

cis-Vaccenoyl-CoA
type: SmallMoleculeReference
xref: Reference/CAS 13673-88-6
xref: Reference/ChEBI CHEBI 75354
xref: Reference/HMDB HMDB0006521
xref: Reference/PubChem-compound 53477847
chemical formula: C39H68N7O17P3S
molecular weight: 1031.3605
structure: ChemicalStructure/PW C002789

Reference/PubChem-compound 1038
type: UnificationXref
id: 1038
db: PubChem-compound

Reference/CAS 18198-76-0
type: UnificationXref
id: 18198-76-0
db: CAS

Reference/GENE ONTOLOGY GO 0005829
type: UnificationXref
id: GO:0005829
db: GENE ONTOLOGY

SubPathwayInteraction78964
type: Interaction
name: SubPathway78964Reaction
name: SubPathwayReaction
participant: Dihydroxyacetone phosphate

Reference/HMDB HMDB0006532
type: UnificationXref
id: HMDB0006532
db: HMDB

Reference/ChEBI CHEBI 16908
type: UnificationXref
id: CHEBI:16908
db: ChEBI

Palmitoleyl-CoA
type: SmallMoleculeReference
xref: Reference/PubChem-compound 53477852
xref: Reference/HMDB HMDB0006532
xref: Reference/ChEBI CHEBI 53152
xref: Reference/CAS 18198-76-0
chemical formula: C37H64N7O17P3S
molecular weight: 1003.3292
structure: ChemicalStructure/PW C002798

Phosphate
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00009
xref: Reference/PubChem-compound 1061
xref: Reference/CAS 14265-44-2
xref: Reference/HMDB HMDB0001429
xref: Reference/BioCyc CPD-8587
xref: Reference/ChEBI CHEBI 18367
xref: Reference/ChemSpider 1032
chemical formula: O4P
molecular weight: 94.95342
structure: ChemicalStructure/PW C001104

TG(16:0/16:1(9Z)/18:1(11Z))
type: SmallMolecule
entity reference: TG(16:0/16:1(9Z)/18:1(11Z))

Reference/ChemSpider 1010
type: UnificationXref
id: 1010
db: ChemSpider

LiPIN (Mammalian lipodystrophy associated) homolog
type: Protein
entity reference: LiPIN (Mammalian lipodystrophy associated) homolog

Compound/PW C002789/Stoichiometry/1.0
type: Stoichiometry
physical entity: cis-Vaccenoyl-CoA
stoichiometric coefficient: 1.0

O-acyltransferase
type: Protein
entity reference: O-acyltransferase

ChemicalStructure/PW C001099
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C003150
type: ChemicalStructure
structure format: SMILES

Compound/PW C003904 Mitochondrial Outer Membrane/Stoichiometry/1.0
type: Stoichiometry
physical entity: LPA(16:0/0:0)
stoichiometric coefficient: 1.0

Reference/BioCyc ACYL-SN-GLYCEROL-3P
type: UnificationXref
id: ACYL-SN-GLYCEROL-3P
db: BioCyc

Protein/14779/Stoichiometry/2.0
type: Stoichiometry
physical entity: Probable glycerol-3-phosphate dehydrogenase 2
stoichiometric coefficient: 2.0

Reference/ChemSpider 7822628
type: UnificationXref
id: 7822628
db: ChemSpider

Probable glycerol-3-phosphate dehydrogenase 2
type: Protein
entity reference: Probable glycerol-3-phosphate dehydrogenase 2

Hydrogen Ion
type: SmallMolecule
entity reference: Hydrogen Ion

Compound/PW C001031/Stoichiometry/1.0
type: Stoichiometry
physical entity: Palmityl-CoA
stoichiometric coefficient: 1.0

Reference/ChEBI CHEBI 15525
type: UnificationXref
id: CHEBI:15525
db: ChEBI

Reference/KEGG Compound C00111
type: UnificationXref
id: C00111
db: KEGG Compound

Cytosol
type: CellularLocationVocabulary
xref: Reference/GENE ONTOLOGY GO 0005829

Reference/PathWhiz PW088465
type: UnificationXref
id: PW088465
db: PathWhiz

ChemicalStructure/PW C002789
type: ChemicalStructure
structure format: SMILES

LPA(16:0/0:0)
type: SmallMolecule
cellular location: Endoplasmic Reticulum Membrane
entity reference: LPA(16:0/0:0)

Reference/CAS 58-68-4
type: UnificationXref
id: 58-68-4
db: CAS

Probable glycerol-3-phosphate acyltransferase, mitochondrial
type: Protein
entity reference: Probable glycerol-3-phosphate acyltransferase, mitochondrial

Putative 1-acyl-sn-glycerol-3-phosphate acyltransferase acl-1
type: Protein
entity reference: Putative 1-acyl-sn-glycerol-3-phosphate acyltransferase acl-1

Reference/HMDB HMDB0001423
type: UnificationXref
id: HMDB0001423
db: HMDB

ChemicalStructure/PW C002798
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C001104
type: ChemicalStructure
structure format: SMILES
structure data: [O-]P([O-])([O-])=O

Reference/KEGG Compound C00009
type: UnificationXref
id: C00009
db: KEGG Compound

Reference/PubChem-compound 53477852
type: UnificationXref
id: 53477852
db: PubChem-compound

Glycolysis
type: Pathway
pathway order: SubPathwayInteractionSteps/SubPathway78964
pathway component: SubPathwayInteraction78964
xref: Reference/SMPDB SMP0087446
xref: Reference/PathWhiz PW088465
name: SubPathway

Reference/KEGG Compound C00001
type: UnificationXref
id: C00001
db: KEGG Compound

Reference/HMDB HMDB0001429
type: UnificationXref
id: HMDB0001429
db: HMDB

Reference/CAS 1763-10-6
type: UnificationXref
id: 1763-10-6
db: CAS

Reference/KEGG Compound C00004
type: UnificationXref
id: C00004
db: KEGG Compound

Reference/ChEBI CHEBI 18367
type: UnificationXref
id: CHEBI:18367
db: ChEBI

Reference/KEGG Compound C00003
type: UnificationXref
id: C00003
db: KEGG Compound

Reference/ChemSpider 1032
type: UnificationXref
id: 1032
db: ChemSpider

LPA(16:0/0:0)
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 15799
xref: Reference/HMDB HMDB0007853
xref: Reference/KEGG Compound C00681
xref: Reference/BioCyc ACYL-SN-GLYCEROL-3P
xref: Reference/ChemSpider 4925335
xref: Reference/PubChem-compound 6419701
chemical formula: C19H39O7P
molecular weight: 410.24335
structure: ChemicalStructure/PW C003904

Glycerol 3-phosphate
type: SmallMoleculeReference
xref: Reference/BioCyc GLYCEROL-3P
xref: Reference/HMDB HMDB0000126
xref: Reference/ChemSpider 388308
xref: Reference/CAS 17989-41-2
xref: Reference/KEGG Compound C00093
xref: Reference/ChEBI CHEBI 15978
xref: Reference/PubChem-compound 439162
chemical formula: C3H9O6P
molecular weight: 172.01367
structure: ChemicalStructure/PW C000081

Reference/SMPDB SMP0087446
type: UnificationXref
id: SMP0087446
db: SMPDB

Reference/CAS 57-04-5
type: UnificationXref
id: 57-04-5
db: CAS

Reference/HMDB HMDB0007099
type: UnificationXref
id: HMDB0007099
db: HMDB

Glycerol 3-phosphate
type: SmallMolecule
entity reference: Glycerol 3-phosphate

NAD
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 15846
xref: Reference/HMDB HMDB0000902
xref: Reference/CAS 53-84-9
xref: Reference/KEGG Compound C00003
xref: Reference/PubChem-compound 5893
xref: Reference/BioCyc NAD
xref: Reference/ChemSpider 5682
chemical formula: C21H28N7O14P2
molecular weight: 664.11694
structure: ChemicalStructure/PW C000721

Reference/UniProt Q93841
type: UnificationXref
id: Q93841
db: UniProt

Reference/KEGG Compound C00010
type: UnificationXref
id: C00010
db: KEGG Compound

LPA(16:0/0:0)
type: SmallMolecule
entity reference: LPA(16:0/0:0)

Reference/HMDB HMDB0000902
type: UnificationXref
id: HMDB0000902
db: HMDB

Reference/BioCyc L-PHOSPHATIDATE
type: UnificationXref
id: L-PHOSPHATIDATE
db: BioCyc

NADH
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0001487
xref: Reference/CAS 58-68-4
xref: Reference/PubChem-compound 439153
xref: Reference/BioCyc NADH
xref: Reference/ChemSpider 388299
xref: Reference/KEGG Compound C00004
xref: Reference/ChEBI CHEBI 16908
chemical formula: C21H29N7O14P2
molecular weight: 665.12476
structure: ChemicalStructure/PW C001144

Reference/ChEBI CHEBI 15978
type: UnificationXref
id: CHEBI:15978
db: ChEBI

Reference/GENE ONTOLOGY GO 0005741
type: UnificationXref
id: GO:0005741
db: GENE ONTOLOGY

Reference/PubChem-compound 6419701
type: UnificationXref
id: 6419701
db: PubChem-compound

Hydrogen Ion
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00080
xref: Reference/ChEBI CHEBI 15378
xref: Reference/HMDB HMDB0059597
xref: Reference/PubChem-compound 1038
xref: Reference/ChemSpider 1010
chemical formula: H
molecular weight: 1.007825
structure: ChemicalStructure/PW C040034

Reference/ChemSpider 388308
type: UnificationXref
id: 388308
db: ChemSpider

Reference/ChEBI CHEBI 84394
type: UnificationXref
id: CHEBI:84394
db: ChEBI

Reference/CAS 53-84-9
type: UnificationXref
id: 53-84-9
db: CAS

Palmityl-CoA
type: SmallMoleculeReference
xref: Reference/PubChem-compound 15667
xref: Reference/ChemSpider 14902
xref: Reference/HMDB HMDB0001338
xref: Reference/ChEBI CHEBI 15525
xref: Reference/KEGG Compound C00154
xref: Reference/CAS 1763-10-6
xref: Reference/BioCyc PALMITYL-COA
chemical formula: C37H66N7O17P3S
molecular weight: 1005.34485
structure: ChemicalStructure/PW C001031

Reference/HMDB HMDB0000126
type: UnificationXref
id: HMDB0000126
db: HMDB

Palmityl-CoA
type: SmallMolecule
entity reference: Palmityl-CoA

Reference/HMDB HMDB0001338
type: UnificationXref
id: HMDB0001338
db: HMDB

Reference/UniProt Q9XXT5
type: UnificationXref
id: Q9XXT5
db: UniProt

Reference/ChemSpider 4925335
type: UnificationXref
id: 4925335
db: ChemSpider

Reference/UniProt Q22949
type: UnificationXref
id: Q22949
db: UniProt

Compound/PW C002798/Stoichiometry/1.0
type: Stoichiometry
physical entity: Palmitoleyl-CoA
stoichiometric coefficient: 1.0

Mitochondrial Outer Membrane
type: CellularLocationVocabulary
xref: Reference/GENE ONTOLOGY GO 0005741

Reference/BioCyc DIACYLGLYCEROL
type: UnificationXref
id: DIACYLGLYCEROL
db: BioCyc

Compound/PW C000721/Stoichiometry/1.0
type: Stoichiometry
physical entity: NAD
stoichiometric coefficient: 1.0

Endoplasmic Reticulum Membrane
type: CellularLocationVocabulary
xref: Reference/GENE ONTOLOGY GO 0005789

Reference/KEGG Compound C00154
type: UnificationXref
id: C00154
db: KEGG Compound

ChemicalStructure/PW C000721
type: ChemicalStructure
structure format: SMILES

Reference/BioCyc CPD-8587
type: UnificationXref
id: CPD-8587
db: BioCyc

Reference/ChemSpider 5682
type: UnificationXref
id: 5682
db: ChemSpider

ChemicalStructure/PW C001144
type: ChemicalStructure
structure format: SMILES

Dihydroxyacetone phosphate
type: SmallMolecule
cellular location: Cytosol
entity reference: Dihydroxyacetone phosphate
name: SubPathwayOutput

Reference/ChEBI CHEBI 1146900
type: UnificationXref
id: CHEBI:1146900
db: ChEBI

Water
type: SmallMolecule
entity reference: Water

Reference/UniProt Q9NCE1
type: UnificationXref
id: Q9NCE1
db: UniProt

Reference/BioCyc CO-A
type: UnificationXref
id: CO-A
db: BioCyc

Reference/KEGG Compound C00165
type: UnificationXref
id: C00165
db: KEGG Compound

Reference/ChemSpider 648
type: UnificationXref
id: 648
db: ChemSpider

Reference/UniProt P34517
type: UnificationXref
id: P34517
db: UniProt

Reaction139156
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001031/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000081/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001099/Stoichiometry/1.0
participant stoichiometry: Compound/PW C003904/Stoichiometry/1.0
right: Coenzyme A
right: LPA(16:0/0:0)
spontaneous: false
left: Palmityl-CoA
left: Glycerol 3-phosphate
name: Glycerol 3-phosphate + Palmityl-CoA → Coenzyme A + LPA(16:0/0:0)
conversion direction: LEFT_TO_RIGHT

Coenzyme A
type: SmallMolecule
entity reference: Coenzyme A

ChemicalStructure/PW C001031
type: ChemicalStructure
structure format: SMILES

Coenzyme A
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 1146900
xref: Reference/HMDB HMDB0001423
xref: Reference/PubChem-compound 6816
xref: Reference/BioCyc CO-A
xref: Reference/ChemSpider 6557
xref: Reference/CAS 85-61-0
xref: Reference/KEGG Compound C00010
chemical formula: C21H36N7O16P3S
molecular weight: 767.11523
structure: ChemicalStructure/PW C001099

ReactionCatalysis128237
type: Catalysis
controller: O-acyltransferase
controlled: Reaction141890
control type: ACTIVATION

ReactionCatalysis128236
type: Catalysis
controller: LiPIN (Mammalian lipodystrophy associated) homolog
controlled: Reaction141885
control type: ACTIVATION

Caenorhabditis elegans
type: BioSource
xref: Reference/TAXONOMY 6239

ReactionCatalysis128235
type: Catalysis
controller: Putative 1-acyl-sn-glycerol-3-phosphate acyltransferase acl-1
controlled: Reaction139269
control type: ACTIVATION

ReactionCatalysis128234
type: Catalysis
controller: Probable glycerol-3-phosphate acyltransferase, mitochondrial
controlled: Reaction139156
control type: ACTIVATION

Reference/PubChem-compound 9543678
type: UnificationXref
id: 9543678
db: PubChem-compound

DG(16:0/16:1(9Z)/0:0)
type: SmallMolecule
entity reference: DG(16:0/16:1(9Z)/0:0)

DG(16:0/16:1(9Z)/0:0)
type: SmallMoleculeReference
xref: Reference/ChemSpider 7822628
xref: Reference/BioCyc DIACYLGLYCEROL
xref: Reference/PubChem-compound 9543678
xref: Reference/ChEBI CHEBI 84394
xref: Reference/KEGG Compound C00165
xref: Reference/HMDB HMDB0007099
chemical formula: C35H66O5
molecular weight: 566.491
structure: ChemicalStructure/PW C003150

Reference/SMPDB SMP0085743
type: UnificationXref
id: SMP0085743
db: SMPDB

Probable glycerol-3-phosphate dehydrogenase 2
type: ProteinReference
xref: Reference/UniProt P34517

Reference/HMDB HMDB0001473
type: UnificationXref
id: HMDB0001473
db: HMDB

Reference/ChemSpider 14902
type: UnificationXref
id: 14902
db: ChemSpider

Reference/TAXONOMY 6239
type: UnificationXref
id: 6239
db: TAXONOMY

O-acyltransferase
type: ProteinReference
xref: Reference/UniProt Q9NCE1

Reference/ChemSpider 6557
type: UnificationXref
id: 6557
db: ChemSpider

LiPIN (Mammalian lipodystrophy associated) homolog
type: ProteinReference
xref: Reference/UniProt Q9XXT5

TG(16:0/16:1(9Z)/18:1(11Z))
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0044060
chemical formula: C53H98O6
molecular weight: 830.7363
structure: ChemicalStructure/PW C024735

Reference/PubChem-compound 668
type: UnificationXref
id: 668
db: PubChem-compound

Putative 1-acyl-sn-glycerol-3-phosphate acyltransferase acl-1
type: ProteinReference
xref: Reference/UniProt Q93841

Probable glycerol-3-phosphate acyltransferase, mitochondrial
type: ProteinReference
xref: Reference/UniProt Q22949

Reference/ChemSpider 388299
type: UnificationXref
id: 388299
db: ChemSpider

Reference/CAS 7732-18-5
type: UnificationXref
id: 7732-18-5
db: CAS

ChemicalStructure/PW C055586
type: ChemicalStructure
structure format: SMILES

Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic
type: Complex
component stoichiometry: Protein/14779/Stoichiometry/2.0
component: Probable glycerol-3-phosphate dehydrogenase 2

Reference/HMDB HMDB0001487
type: UnificationXref
id: HMDB0001487
db: HMDB

Compound/PW C001134/Stoichiometry/1.0
type: Stoichiometry
physical entity: Dihydroxyacetone phosphate
stoichiometric coefficient: 1.0

ReactionCatalysis128202
type: Catalysis
controller: Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic
controlled: Reaction138125
control type: ACTIVATION

Reference/GENE ONTOLOGY GO 0005789
type: UnificationXref
id: GO:0005789
db: GENE ONTOLOGY

Compound/PW C003904 Endoplasmic Reticulum Membrane/Stoichiometry/1.0
type: Stoichiometry
physical entity: LPA(16:0/0:0)
stoichiometric coefficient: 1.0

Reaction139269
type: BiochemicalReaction
participant stoichiometry: Compound/PW C002798/Stoichiometry/1.0
participant stoichiometry: Compound/PW C055586/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001099/Stoichiometry/1.0
participant stoichiometry: Compound/PW C003904/Stoichiometry/1.0
right: Coenzyme A
right: PA(16:0/16:1(9Z))
spontaneous: false
left: LPA(16:0/0:0)
left: Palmitoleyl-CoA
name: LPA(16:0/0:0) + Palmitoleyl-CoA → Coenzyme A + PA(16:0/16:1(9Z))
conversion direction: LEFT_TO_RIGHT

Reference/PubChem-compound 53477847
type: UnificationXref
id: 53477847
db: PubChem-compound

Reference/ChEBI CHEBI 15799
type: UnificationXref
id: CHEBI:15799
db: ChEBI

Reference/BioCyc DIHYDROXY-ACETONE-PHOSPHATE
type: UnificationXref
id: DIHYDROXY-ACETONE-PHOSPHATE
db: BioCyc

Compound/PW C001099/Stoichiometry/1.0
type: Stoichiometry
physical entity: Coenzyme A
stoichiometric coefficient: 1.0

Compound/PW C001144/Stoichiometry/1.0
type: Stoichiometry
physical entity: NADH
stoichiometric coefficient: 1.0

Reference/HMDB HMDB0044060
type: UnificationXref
id: HMDB0044060
db: HMDB

ChemicalStructure/PW C001134
type: ChemicalStructure
structure format: SMILES
structure data: OCC(=O)COP(O)(O)=O

Reference/PubChem-compound 962
type: UnificationXref
id: 962
db: PubChem-compound

Reference/ChEBI CHEBI 16337
type: UnificationXref
id: CHEBI:16337
db: ChEBI

ChemicalStructure/PW C024735
type: ChemicalStructure
structure format: SMILES

Palmitoleyl-CoA
type: SmallMolecule
entity reference: Palmitoleyl-CoA

Phosphate
type: SmallMolecule
entity reference: Phosphate

Reference/PubChem-compound 5893
type: UnificationXref
id: 5893
db: PubChem-compound

Compound/PW C001104/Stoichiometry/1.0
type: Stoichiometry
physical entity: Phosphate
stoichiometric coefficient: 1.0

PA(16:0/16:1(9Z))
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00416
xref: Reference/BioCyc L-PHOSPHATIDATE
xref: Reference/ChEBI CHEBI 16337
chemical formula: C35H67O8P
molecular weight: 646.45734
structure: ChemicalStructure/PW C055586

Reference/KEGG Compound C00080
type: UnificationXref
id: C00080
db: KEGG Compound

Reference/HMDB HMDB0002111
type: UnificationXref
id: HMDB0002111
db: HMDB

Reference/ChEBI CHEBI 15377
type: UnificationXref
id: CHEBI:15377
db: ChEBI

Reference/ChEBI CHEBI 15378
type: UnificationXref
id: CHEBI:15378
db: ChEBI

ChemicalStructure/PW C040034
type: ChemicalStructure
structure format: SMILES
structure data: [H+]

Reference/CAS 14265-44-2
type: UnificationXref
id: 14265-44-2
db: CAS

Reference/ChEBI CHEBI 16108
type: UnificationXref
id: CHEBI:16108
db: ChEBI

Reference/CAS 17989-41-2
type: UnificationXref
id: 17989-41-2
db: CAS

cis-Vaccenoyl-CoA
type: SmallMolecule
entity reference: cis-Vaccenoyl-CoA

Compound/PW C001420/Stoichiometry/1.0
type: Stoichiometry
physical entity: Water
stoichiometric coefficient: 1.0

Reference/BioCyc GLYCEROL-3P
type: UnificationXref
id: GLYCEROL-3P
db: BioCyc

Reference/KEGG Compound C00093
type: UnificationXref
id: C00093
db: KEGG Compound

Reference/KEGG Compound C00416
type: UnificationXref
id: C00416
db: KEGG Compound

LPA(16:0/0:0)
type: SmallMolecule
cellular location: Mitochondrial Outer Membrane
entity reference: LPA(16:0/0:0)

Water
type: SmallMoleculeReference
xref: Reference/PubChem-compound 962
xref: Reference/ChEBI CHEBI 15377
xref: Reference/KEGG Compound C00001
xref: Reference/ChemSpider 937
xref: Reference/HMDB HMDB0002111
xref: Reference/CAS 7732-18-5
chemical formula: H2O
molecular weight: 18.010565
structure: ChemicalStructure/PW C001420

Reference/BioCyc NADH
type: UnificationXref
id: NADH
db: BioCyc

Reference/BioCyc NAD
type: UnificationXref
id: NAD
db: BioCyc

Reference/PubChem-compound 15667
type: UnificationXref
id: 15667
db: PubChem-compound

Reference/PubChem-compound 1061
type: UnificationXref
id: 1061
db: PubChem-compound

Compound/PW C024735/Stoichiometry/1.0
type: Stoichiometry
physical entity: TG(16:0/16:1(9Z)/18:1(11Z))
stoichiometric coefficient: 1.0

Reference/CAS 13673-88-6
type: UnificationXref
id: 13673-88-6
db: CAS

Reference/HMDB HMDB0059597
type: UnificationXref
id: HMDB0059597
db: HMDB

Compound/PW C000081/Stoichiometry/1.0
type: Stoichiometry
physical entity: Glycerol 3-phosphate
stoichiometric coefficient: 1.0

ChemicalStructure/PW C003904
type: ChemicalStructure
structure format: SMILES
structure data: CCCCCCCCCCCCCCCC(=O)OCC(O)COP(O)(O)=O

Reference/ChEBI CHEBI 53152
type: UnificationXref
id: CHEBI:53152
db: ChEBI

Reaction141890
type: BiochemicalReaction
participant stoichiometry: Compound/PW C003150/Stoichiometry/1.0
participant stoichiometry: Compound/PW C024735/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001099/Stoichiometry/1.0
participant stoichiometry: Compound/PW C002789/Stoichiometry/1.0
right: Coenzyme A
right: TG(16:0/16:1(9Z)/18:1(11Z))
spontaneous: false
left: DG(16:0/16:1(9Z)/0:0)
left: cis-Vaccenoyl-CoA
name: DG(16:0/16:1(9Z)/0:0) + cis-Vaccenoyl-CoA → Coenzyme A + TG(16:0/16:1(9Z)/18:1(11Z))
conversion direction: LEFT_TO_RIGHT

Reaction138125
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001134/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000721/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000081/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001144/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: NAD
right: Glycerol 3-phosphate
spontaneous: false
left: NADH
left: Dihydroxyacetone phosphate
left: Hydrogen Ion
name: Dihydroxyacetone phosphate + Hydrogen Ion + NADH → Glycerol 3-phosphate + NAD
conversion direction: LEFT_TO_RIGHT

Reference/CAS 85-61-0
type: UnificationXref
id: 85-61-0
db: CAS

ChemicalStructure/PW C000081
type: ChemicalStructure
structure format: SMILES
structure data: OC[C@@H](O)COP(O)(O)=O