Glycerol-3-phosphate O-acyltransferase 2
type: Protein
entity reference: Glycerol-3-phosphate O-acyltransferase 2

Glycerol-3-phosphate O-acyltransferase 1
type: Protein
entity reference: Glycerol-3-phosphate O-acyltransferase 1

Reaction187406
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: REVERSIBLE

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

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

Reference/BioCyc L-1-PHOSPHATIDYL-GLYCEROL-P
type: UnificationXref
id: L-1-PHOSPHATIDYL-GLYCEROL-P
db: BioCyc

Reference/UniProt Q05776
type: UnificationXref
id: Q05776
db: UniProt

Capric acid
type: SmallMoleculeReference
xref: Reference/PubChem-compound 2969
xref: Reference/BioCyc 3-OXODODECANOATE
xref: Reference/ChEBI CHEBI 30813
xref: Reference/HMDB HMDB0000511
xref: Reference/ChemSpider 2863
xref: Reference/KEGG Compound C01571
xref: Reference/CAS 334-48-5
chemical formula: C10H20O2
molecular weight: 172.14633
structure: ChemicalStructure/PW C000391

NADH
type: SmallMolecule
entity reference: NADH

PA(10:0/16:1(9Z))
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00416
xref: Reference/BioCyc L-PHOSPHATIDATE
xref: Reference/ChEBI CHEBI 16337
chemical formula: C29H55O8P
molecular weight: 562.36346
structure: ChemicalStructure/PW C055535

Reference/UniProt Q06508
type: UnificationXref
id: Q06508
db: UniProt

Cytidine triphosphate
type: SmallMolecule
entity reference: Cytidine triphosphate

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

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

Reference/HMDB HMDB0000095
type: UnificationXref
id: HMDB0000095
db: HMDB

Pyrophosphate
type: SmallMolecule
entity reference: Pyrophosphate

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

Reference/PubChem-compound 6131
type: UnificationXref
id: 6131
db: PubChem-compound

Compound/PW C000064/Stoichiometry/1.0
type: Stoichiometry
physical entity: Cytidine monophosphate
stoichiometric coefficient: 1.0

NAD
type: SmallMolecule
entity reference: NAD

Compound/PW C055535/Stoichiometry/1.0
type: Stoichiometry
physical entity: PA(10:0/16:1(9Z))
stoichiometric coefficient: 1.0

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

Reference/UniProt Q06510
type: UnificationXref
id: Q06510
db: UniProt

ChemicalStructure/PW C105082
type: ChemicalStructure
structure format: SMILES

MLCL(0:0/16:1(9Z)/18:1(11Z)/28:1(9Z))
type: SmallMoleculeReference
chemical formula: C71H134O16P2
molecular weight: 1304.9147
structure: ChemicalStructure/PW C107173

Compound/PW C047890/Stoichiometry/1.0
type: Stoichiometry
physical entity: CL(10:0/16:1(9Z)/18:1(11Z)/28:1(9Z))
stoichiometric coefficient: 1.0

PC(10:0/10:0)
type: SmallMoleculeReference
chemical formula: C28H56NO8P
molecular weight: 565.3743
structure: ChemicalStructure/PW C055665

Dihydroxyacetone phosphate
type: SmallMolecule
entity reference: Dihydroxyacetone phosphate

Reference/BioCyc 3-OXODODECANOATE
type: UnificationXref
id: 3-OXODODECANOATE
db: BioCyc

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

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/HMDB HMDB0006404
type: UnificationXref
id: HMDB0006404
db: HMDB

2.3.1.23
type: BiochemicalReaction
participant stoichiometry: Compound/PW C002798/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001099/Stoichiometry/1.0
participant stoichiometry: Compound/PW C055535/Stoichiometry/1.0
participant stoichiometry: Compound/PW C055362/Stoichiometry/1.0
right: PA(10:0/16:1(9Z))
right: Coenzyme A
spontaneous: false
EC number: 2.3.1.23
left: LysoPA(10:0/0:0)
left: Palmitoleyl-CoA
name: LysoPA(10:0/0:0) + Palmitoleyl-CoA → Coenzyme A + PA(10:0/16:1(9Z))
conversion direction: LEFT_TO_RIGHT

2.7.8.5
type: BiochemicalReaction
participant stoichiometry: Compound/PW C042689/Stoichiometry/1.0
participant stoichiometry: Compound/PW C105051/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000064/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000081/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Cytidine monophosphate
right: PGP(10:0/16:1(9Z))
right: Hydrogen Ion
spontaneous: false
EC number: 2.7.8.5
left: CDP-DG(10:0/16:1(9Z))
left: Glycerol 3-phosphate
name: CDP-DG(10:0/16:1(9Z)) + Glycerol 3-phosphate → Cytidine monophosphate + Hydrogen Ion + PGP(10:0/16:1(9Z))
conversion direction: LEFT_TO_RIGHT

Reference/ChemSpider 559142
type: UnificationXref
id: 559142
db: ChemSpider

3.1.3.27
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C105051/Stoichiometry/1.0
participant stoichiometry: Compound/PW C105082/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001104/Stoichiometry/1.0
right: PG(10:0/16:1(9Z))
right: Phosphate
spontaneous: false
EC number: 3.1.3.27
left: PGP(10:0/16:1(9Z))
left: Water
name: PGP(10:0/16:1(9Z)) + Water → PG(10:0/16:1(9Z)) + Phosphate
conversion direction: LEFT_TO_RIGHT

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

CDP-DG(18:1(11Z)/28:1(9Z))
type: SmallMolecule
entity reference: CDP-DG(18:1(11Z)/28:1(9Z))

Compound/PW C055362/Stoichiometry/1.0
type: Stoichiometry
physical entity: LysoPA(10:0/0:0)
stoichiometric coefficient: 1.0

Reference/UniProt P41911
type: UnificationXref
id: P41911
db: UniProt

CDP-DG(18:1(11Z)/28:1(9Z))
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 17962
xref: Reference/BioCyc CDPDIACYLGLYCEROL
xref: Reference/KEGG Compound C00269
chemical formula: C58H105N3O15P2
molecular weight: 1145.7021
structure: ChemicalStructure/PW C045630

Lysophosphatidylcholine acyltransferase
type: ProteinReference
xref: Reference/UniProt Q06510

Compound/PW C105051/Stoichiometry/1.0
type: Stoichiometry
physical entity: PGP(10:0/16:1(9Z))
stoichiometric coefficient: 1.0

PA(10:0/16:1(9Z))
type: SmallMolecule
cellular location: Mitochondrial Outer Membrane
entity reference: PA(10:0/16:1(9Z))

Reference/UniProt Q12043
type: UnificationXref
id: Q12043
db: UniProt

Compound/PW C055535 Mitochondrial Outer Membrane/Stoichiometry/1.0
type: Stoichiometry
physical entity: PA(10:0/16:1(9Z))
stoichiometric coefficient: 1.0

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

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

Capric acid
type: SmallMolecule
entity reference: Capric acid

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: H3O4P
molecular weight: 97.9769
structure: ChemicalStructure/PW C001104

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

Reference/KEGG Compound C00344
type: UnificationXref
id: C00344
db: KEGG Compound

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

Saccharomyces cerevisiae
type: BioSource
xref: Reference/TAXONOMY 4932

ChemicalStructure/PW C001099
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C002742
type: ChemicalStructure
structure format: SMILES

2.7.8.41
type: BiochemicalReaction
participant stoichiometry: Compound/PW C047890/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045630/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000064/Stoichiometry/1.0
participant stoichiometry: Compound/PW C105082/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Cytidine monophosphate
right: Hydrogen Ion
right: CL(10:0/16:1(9Z)/18:1(11Z)/28:1(9Z))
spontaneous: false
EC number: 2.7.8.41
left: PG(10:0/16:1(9Z))
left: CDP-DG(18:1(11Z)/28:1(9Z))
name: CDP-DG(18:1(11Z)/28:1(9Z)) + PG(10:0/16:1(9Z)) → CL(10:0/16:1(9Z)/18:1(11Z)/28:1(9Z)) + Cytidine monophosphate + Hydrogen Ion
conversion direction: LEFT_TO_RIGHT

2.3.1.23
type: BiochemicalReaction
participant stoichiometry: Compound/PW C047890/Stoichiometry/1.0
participant stoichiometry: Compound/PW C108327/Stoichiometry/1.0
participant stoichiometry: Compound/PW C107173/Stoichiometry/1.0
participant stoichiometry: Compound/PW C055665/Stoichiometry/1.0
right: LysoPC(10:0/0:0)
right: CL(10:0/16:1(9Z)/18:1(11Z)/28:1(9Z))
spontaneous: false
EC number: 2.3.1.23
left: MLCL(0:0/16:1(9Z)/18:1(11Z)/28:1(9Z))
left: PC(10:0/10:0)
name: MLCL(0:0/16:1(9Z)/18:1(11Z)/28:1(9Z)) + PC(10:0/10:0) → CL(10:0/16:1(9Z)/18:1(11Z)/28:1(9Z)) + LysoPC(10:0/0:0)
conversion direction: LEFT_TO_RIGHT

3.5.1.-
type: BiochemicalReaction
participant stoichiometry: Compound/PW C047890/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000391/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C107173/Stoichiometry/1.0
right: MLCL(0:0/16:1(9Z)/18:1(11Z)/28:1(9Z))
right: Capric acid
spontaneous: false
EC number: 3.5.1.-
left: Water
left: CL(10:0/16:1(9Z)/18:1(11Z)/28:1(9Z))
name: CL(10:0/16:1(9Z)/18:1(11Z)/28:1(9Z)) + Water → Capric acid + MLCL(0:0/16:1(9Z)/18:1(11Z)/28:1(9Z))
conversion direction: LEFT_TO_RIGHT

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

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

Reference/CAS 63-37-6
type: UnificationXref
id: 63-37-6
db: CAS

Compound/PW C045630/Stoichiometry/1.0
type: Stoichiometry
physical entity: CDP-DG(18:1(11Z)/28:1(9Z))
stoichiometric coefficient: 1.0

Reference/ChEBI CHEBI 16975
type: UnificationXref
id: CHEBI:16975
db: ChEBI

Hydrogen Ion
type: SmallMolecule
entity reference: Hydrogen Ion

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

ChemicalStructure/PW C055362
type: ChemicalStructure
structure format: SMILES
structure data: CCCCCCCCCC(=O)OCC(O)COP(O)(O)=O

Cardiolipin synthase (CMP-forming)
type: Protein
entity reference: Cardiolipin synthase (CMP-forming)

Phosphatidate cytidylyltransferase
type: Complex
component: Phosphatidate cytidylyltransferase
component: Phosphatidate cytidylyltransferase, mitochondrial

PG(10:0/16:1(9Z))
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 17517
xref: Reference/BioCyc L-1-PHOSPHATIDYL-GLYCEROL
xref: Reference/KEGG Compound C00344
chemical formula: C32H61O10P
molecular weight: 636.4002
structure: ChemicalStructure/PW C105082

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

ERMES COMPLEX
type: Complex
component: Maintenance of mitochondrial morphology protein 1
component: Mitochondrial distribution and morphology protein 12
component: Mitochondrial distribution and morphology protein 10
component: Mitochondrial distribution and morphology protein 34

Ups1/Mdm35p heterodimer
type: Complex
component: Protein UPS1, mitochondrial
component: Mitochondrial distribution and morphology protein 35

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

PA(10:0/16:1(9Z))
type: SmallMolecule
entity reference: PA(10:0/16:1(9Z))

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

ChemicalStructure/PW C002798
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C107173
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C001104
type: ChemicalStructure
structure format: SMILES
structure data: OP(O)(O)=O

Compound/PW C108327/Stoichiometry/1.0
type: Stoichiometry
physical entity: LysoPC(10:0/0:0)
stoichiometric coefficient: 1.0

Compound/PW C000057/Stoichiometry/1.0
type: Stoichiometry
physical entity: Cytidine triphosphate
stoichiometric coefficient: 1.0

Reference/UniProt P53083
type: UnificationXref
id: P53083
db: UniProt

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

Protein UPS1, mitochondrial
type: Protein
entity reference: Protein UPS1, mitochondrial

Mitochondrial distribution and morphology protein 35
type: Protein
entity reference: Mitochondrial distribution and morphology protein 35

Phosphatidate cytidylyltransferase
type: Protein
entity reference: Phosphatidate cytidylyltransferase

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

Phosphatidate cytidylyltransferase, mitochondrial
type: Protein
entity reference: Phosphatidate cytidylyltransferase, mitochondrial

CDP-DG(10:0/16:1(9Z))
type: SmallMolecule
entity reference: CDP-DG(10:0/16:1(9Z))

Maintenance of mitochondrial morphology protein 1
type: Protein
entity reference: Maintenance of mitochondrial morphology protein 1

Mitochondrial distribution and morphology protein 12
type: Protein
entity reference: Mitochondrial distribution and morphology protein 12

Reference/PathWhiz PW005543
type: UnificationXref
id: PW005543
db: PathWhiz

Mitochondrial distribution and morphology protein 10
type: Protein
entity reference: Mitochondrial distribution and morphology protein 10

Mitochondrial distribution and morphology protein 34
type: Protein
entity reference: Mitochondrial distribution and morphology protein 34

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

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

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

Reference/PubChem-compound 440615
type: UnificationXref
id: 440615
db: PubChem-compound

Reference/ChEBI CHEBI 18361
type: UnificationXref
id: CHEBI:18361
db: ChEBI

Reference/KEGG Compound C01571
type: UnificationXref
id: C01571
db: KEGG Compound

Compound/PW C055535 Endoplasmic Reticulum Membrane/Stoichiometry/1.0
type: Stoichiometry
physical entity: PA(10:0/16:1(9Z))
stoichiometric coefficient: 1.0

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

Reference/UniProt P18409
type: UnificationXref
id: P18409
db: UniProt

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

2.3.1.15
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000081/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001099/Stoichiometry/1.0
participant stoichiometry: Compound/PW C002742/Stoichiometry/1.0
participant stoichiometry: Compound/PW C055362/Stoichiometry/1.0
right: Coenzyme A
right: LysoPA(10:0/0:0)
spontaneous: false
EC number: 2.3.1.15
left: Decanoyl-CoA
left: Glycerol 3-phosphate
name: Decanoyl-CoA + Glycerol 3-phosphate → Coenzyme A + LysoPA(10:0/0:0)
conversion direction: LEFT_TO_RIGHT

PC(10:0/10:0)
type: SmallMolecule
entity reference: PC(10:0/10:0)

Mitochondrial Inner Membrane
type: CellularLocationVocabulary
xref: Reference/GENE ONTOLOGY GO 0005743

Glycerol-3-phosphate O-acyltransferase 2
type: ProteinReference
xref: Reference/UniProt P36148

ReactionCatalysis6422
type: Catalysis
controller: Phosphatidylglycerophosphatase GEP4, mitochondrial
controlled: 3.1.3.27
control type: ACTIVATION

Glycerol-3-phosphate O-acyltransferase 1
type: ProteinReference
xref: Reference/UniProt P32784

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

CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase
type: Protein
entity reference: CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase

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

Phosphatidylglycerophosphatase GEP4, mitochondrial
type: Protein
entity reference: Phosphatidylglycerophosphatase GEP4, mitochondrial

Acyl-CoA:lyso-phospholipid acyltransferase
type: ProteinReference
xref: Reference/UniProt Q08548

Probable 1-acyl-sn-glycerol-3-phosphate acyltransferase
type: ProteinReference
xref: Reference/UniProt P33333

Lipase 4
type: ProteinReference
xref: Reference/UniProt P36165

CDP-DG(10:0/16:1(9Z))
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 17962
xref: Reference/BioCyc CDPDIACYLGLYCEROL
xref: Reference/KEGG Compound C00269
chemical formula: C38H67N3O15P2
molecular weight: 867.4047
structure: ChemicalStructure/PW C042689

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: C21H27N7O14P2
molecular weight: 663.10913
structure: ChemicalStructure/PW C000721

PA(10:0/16:1(9Z))
type: SmallMolecule
cellular location: Mitochondrial Inner Membrane
entity reference: PA(10:0/16:1(9Z))

Reference/ChEBI CHEBI 17361
type: UnificationXref
id: CHEBI:17361
db: ChEBI

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

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

Reference/KEGG Compound C00013
type: UnificationXref
id: C00013
db: KEGG Compound

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

Reference/KEGG Compound C05274
type: UnificationXref
id: C05274
db: KEGG Compound

Pyrophosphate
type: SmallMoleculeReference
xref: Reference/PubChem-compound 644102
xref: Reference/BioCyc PPI
xref: Reference/ChemSpider 559142
xref: Reference/ChEBI CHEBI 18361
xref: Reference/HMDB HMDB0000250
xref: Reference/CAS 14000-31-8
xref: Reference/KEGG Compound C00013
chemical formula: H4O7P2
molecular weight: 177.94322
structure: ChemicalStructure/PW C000170

PGP(10:0/16:1(9Z))
type: SmallMolecule
entity reference: PGP(10:0/16:1(9Z))

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

Cardiolipin-specific deacylase 1, mitochondrial
type: ProteinReference
xref: Reference/UniProt P53264

Glycerol-3-phosphate dehydrogenase
type: Complex
component: Glycerol-3-phosphate dehydrogenase
component: Glycerol-3-phosphate dehydrogenase GPD2

LysoPC(10:0/0:0)
type: SmallMolecule
entity reference: LysoPC(10:0/0:0)

Reference/GENE ONTOLOGY GO 0005743
type: UnificationXref
id: GO:0005743
db: GENE ONTOLOGY

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

Cytidine triphosphate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 17677
xref: Reference/CAS 65-47-4
xref: Reference/PubChem-compound 6176
xref: Reference/KEGG Compound C00063
xref: Reference/ChemSpider 5941
xref: Reference/HMDB HMDB0000082
xref: Reference/BioCyc CTP
chemical formula: C9H16N3O14P3
molecular weight: 482.9845
structure: ChemicalStructure/PW C000057

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

Lysophosphatidic acid:oleoyl-CoA acyltransferase 1
type: ProteinReference
xref: Reference/UniProt Q06508

Lipase 5
type: ProteinReference
xref: Reference/UniProt Q12043

Reference/CAS 334-48-5
type: UnificationXref
id: 334-48-5
db: CAS

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/UniProt P38812
type: UnificationXref
id: P38812
db: UniProt

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

Glycerol-3-phosphate dehydrogenase
type: Protein
entity reference: Glycerol-3-phosphate dehydrogenase

Glycerol-3-phosphate dehydrogenase GPD2
type: Protein
entity reference: Glycerol-3-phosphate dehydrogenase GPD2

Reference/BioCyc L-1-PHOSPHATIDYL-GLYCEROL
type: UnificationXref
id: L-1-PHOSPHATIDYL-GLYCEROL
db: BioCyc

Transport10458
type: Transport
participant stoichiometry: Compound/PW C055535 Mitochondrial Outer Membrane/Stoichiometry/1.0
participant stoichiometry: Compound/PW C055535 Endoplasmic Reticulum Membrane/Stoichiometry/1.0
right: PA(10:0/16:1(9Z))
spontaneous: false
left: PA(10:0/16:1(9Z))
name: PA(10:0/16:1(9Z)) (→) Transport: Saccharomyces cerevisiae, Cell, Endoplasmic Reticulum Membrane to Saccharomyces cerevisiae, Cell, Mitochondrial Outer Membrane
conversion direction: LEFT_TO_RIGHT

Transport10459
type: Transport
participant stoichiometry: Compound/PW C055535 Mitochondrial Outer Membrane/Stoichiometry/1.0
participant stoichiometry: Compound/PW C055535 Mitochondrial Inner Membrane/Stoichiometry/1.0
right: PA(10:0/16:1(9Z))
spontaneous: false
left: PA(10:0/16:1(9Z))
name: PA(10:0/16:1(9Z)) (→) Transport: Saccharomyces cerevisiae, Cell, Mitochondrial Outer Membrane to Saccharomyces cerevisiae, Cell, Mitochondrial Inner Membrane
conversion direction: LEFT_TO_RIGHT

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

Reference/ChemSpider 389510
type: UnificationXref
id: 389510
db: ChemSpider

Reference/KEGG Compound C00269
type: UnificationXref
id: C00269
db: KEGG Compound

PGP(10:0/16:1(9Z))
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 37393
xref: Reference/BioCyc L-1-PHOSPHATIDYL-GLYCEROL-P
xref: Reference/KEGG Compound C03892
chemical formula: C32H62O13P2
molecular weight: 716.3666
structure: ChemicalStructure/PW C105051

Reference/KEGG Compound C03892
type: UnificationXref
id: C03892
db: KEGG Compound

Cytidine monophosphate
type: SmallMolecule
entity reference: Cytidine monophosphate

ChemicalStructure/PW C047890
type: ChemicalStructure
structure format: SMILES

Cardiolipin Biosynthesis CL(10:0/16:1(9Z)/18:1(11Z)/28:1(9Z))
type: Pathway
pathway order: PathwayEnzymeReaction/2235248
pathway order: PathwayEnzymeReaction/2235249
pathway order: PathwayEnzymeReaction/2235253
pathway order: PathwayEnzymeReaction/2235254
pathway order: PathwayEnzymeReaction/2235255
pathway order: PathwayEnzymeReaction/2235256
pathway order: PathwayEnzymeReaction/2235250
pathway order: PathwayEnzymeReaction/2235251
pathway order: PathwayEnzymeReaction/2235252
pathway order: PathwayTransport/2235257
pathway order: PathwayTransport/2235258
pathway component: ReactionCatalysis177070
pathway component: ReactionCatalysis177071
pathway component: Reaction187406
pathway component: Transport10458
pathway component: Transport10459
pathway component: TransportCatalysis1609
pathway component: TransportCatalysis1608
pathway component: 2.3.1.15
pathway component: 2.7.8.41
pathway component: 2.3.1.23
pathway component: 2.7.8.5
pathway component: 3.5.1.-
pathway component: 3.1.3.27
pathway component: ReactionCatalysis177066
pathway component: ReactionCatalysis6422
pathway component: ReactionCatalysis177067
pathway component: ReactionCatalysis177078
pathway component: ReactionCatalysis177068
pathway component: 2.7.7.41
pathway component: ReactionCatalysis177075
pathway component: ReactionCatalysis177065
xref: Reference/PathWhiz PW005543
xref: Reference/SMPDB SMP0004745
organism: Saccharomyces cerevisiae

Reference/CAS 1264-57-9
type: UnificationXref
id: 1264-57-9
db: CAS

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

ReactionCatalysis177066
type: Catalysis
controller: Glycerol-3-phosphate O-acyltransferase
controlled: 2.3.1.15
control type: ACTIVATION

ReactionCatalysis177067
type: Catalysis
controller: Lysophosphatidate acyltransferase
controlled: 2.3.1.23
control type: ACTIVATION

Reference/ChEBI CHEBI 28493
type: UnificationXref
id: CHEBI:28493
db: ChEBI

ReactionCatalysis177068
type: Catalysis
controller: Phosphatidate cytidylyltransferase
controlled: 2.7.7.41
control type: ACTIVATION

Reference/ChEBI CHEBI 28494
type: UnificationXref
id: CHEBI:28494
db: ChEBI

Cytidine monophosphate
type: SmallMoleculeReference
xref: Reference/BioCyc CMP
xref: Reference/ChemSpider 5901
xref: Reference/PubChem-compound 6131
xref: Reference/ChEBI CHEBI 17361
xref: Reference/KEGG Compound C00055
xref: Reference/HMDB HMDB0000095
xref: Reference/CAS 63-37-6
chemical formula: C9H14N3O8P
molecular weight: 323.05185
structure: ChemicalStructure/PW C000064

ReactionCatalysis177065
type: Catalysis
controller: Glycerol-3-phosphate dehydrogenase
controlled: Reaction187406
control type: ACTIVATION

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

ReactionCatalysis177070
type: Catalysis
controller: CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase
controlled: 2.7.8.5
control type: ACTIVATION

ReactionCatalysis177071
type: Catalysis
controller: Cardiolipin synthase (CMP-forming)
controlled: 2.7.8.41
control type: ACTIVATION

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

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

Reference/UniProt P36148
type: UnificationXref
id: P36148
db: UniProt

Compound/PW C107173/Stoichiometry/1.0
type: Stoichiometry
physical entity: MLCL(0:0/16:1(9Z)/18:1(11Z)/28:1(9Z))
stoichiometric coefficient: 1.0

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

Compound/PW C055535 Mitochondrial Inner Membrane/Stoichiometry/1.0
type: Stoichiometry
physical entity: PA(10:0/16:1(9Z))
stoichiometric coefficient: 1.0

ChemicalStructure/PW C000721
type: ChemicalStructure
structure format: SMILES

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

TransportCatalysis1609
type: Catalysis
controller: Ups1/Mdm35p heterodimer
controlled: Transport10459
control type: ACTIVATION

TransportCatalysis1608
type: Catalysis
controller: ERMES COMPLEX
controlled: Transport10458
control type: ACTIVATION

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

ChemicalStructure/PW C001144
type: ChemicalStructure
structure format: SMILES

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

Water
type: SmallMolecule
entity reference: Water

CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase
type: ProteinReference
xref: Reference/UniProt P25578

Phosphatidate cytidylyltransferase, mitochondrial
type: ProteinReference
xref: Reference/UniProt P53230

ChemicalStructure/PW C000057
type: ChemicalStructure
structure format: SMILES

Phosphatidylglycerophosphatase GEP4, mitochondrial
type: ProteinReference
xref: Reference/UniProt P38812

Protein UPS1, mitochondrial
type: ProteinReference
xref: Reference/UniProt Q05776

ReactionCatalysis177078
type: Catalysis
controller: Cardiolipin-specific deacylase 1, mitochondrial
controlled: 3.5.1.-
control type: ACTIVATION

Mitochondrial distribution and morphology protein 34
type: ProteinReference
xref: Reference/UniProt P53083

Phosphatidate cytidylyltransferase
type: ProteinReference
xref: Reference/UniProt P38221

LysoPC(10:0/0:0)
type: SmallMoleculeReference
xref: Reference/KEGG Compound C04230
xref: Reference/BioCyc PHOSPHATIDYLCHOLINE
chemical formula: C18H38NO7P
molecular weight: 411.2386
structure: ChemicalStructure/PW C108327

Mitochondrial distribution and morphology protein 35
type: ProteinReference
xref: Reference/UniProt O60200

Maintenance of mitochondrial morphology protein 1
type: ProteinReference
xref: Reference/UniProt P41800

Reference/HMDB HMDB0000250
type: UnificationXref
id: HMDB0000250
db: HMDB

ChemicalStructure/PW C000170
type: ChemicalStructure
structure format: SMILES
structure data: OP(O)(=O)OP(O)(O)=O

ReactionCatalysis177075
type: Catalysis
controller: Lysophosphatidylcholine acyltransferase
controlled: 2.3.1.23
control type: ACTIVATION

Mitochondrial distribution and morphology protein 10
type: ProteinReference
xref: Reference/UniProt P18409

Reference/CAS 14000-31-8
type: UnificationXref
id: 14000-31-8
db: CAS

Mitochondrial distribution and morphology protein 12
type: ProteinReference
xref: Reference/UniProt Q92328

Reference/ChEBI CHEBI 17517
type: UnificationXref
id: CHEBI:17517
db: ChEBI

Reference/UniProt Q07560
type: UnificationXref
id: Q07560
db: UniProt

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

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

Decanoyl-CoA
type: SmallMolecule
entity reference: Decanoyl-CoA

Coenzyme A
type: SmallMolecule
entity reference: Coenzyme A

ChemicalStructure/PW C000064
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

Compound/PW C000170/Stoichiometry/1.0
type: Stoichiometry
physical entity: Pyrophosphate
stoichiometric coefficient: 1.0

Reference/KEGG Compound C05980
type: UnificationXref
id: C05980
db: KEGG Compound

Decanoyl-CoA
type: SmallMoleculeReference
xref: Reference/KEGG Compound C05274
xref: Reference/CAS 1264-57-9
xref: Reference/HMDB HMDB0006404
xref: Reference/PubChem-compound 440615
xref: Reference/ChEBI CHEBI 28493
xref: Reference/ChemSpider 389510
chemical formula: C31H54N7O17P3S
molecular weight: 921.251
structure: ChemicalStructure/PW C002742

CL(10:0/16:1(9Z)/18:1(11Z)/28:1(9Z))
type: SmallMoleculeReference
xref: Reference/KEGG Compound C05980
xref: Reference/ChEBI CHEBI 28494
xref: Reference/BioCyc CARDIOLIPIN
chemical formula: C81H152O17P2
molecular weight: 1459.0505
structure: ChemicalStructure/PW C047890

2.7.7.41
type: BiochemicalReaction
participant stoichiometry: Compound/PW C042689/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000170/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000057/Stoichiometry/1.0
participant stoichiometry: Compound/PW C055535/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: CDP-DG(10:0/16:1(9Z))
right: Pyrophosphate
spontaneous: false
EC number: 2.7.7.41
left: PA(10:0/16:1(9Z))
left: Cytidine triphosphate
left: Hydrogen Ion
name: Cytidine triphosphate + Hydrogen Ion + PA(10:0/16:1(9Z)) → CDP-DG(10:0/16:1(9Z)) + Pyrophosphate
conversion direction: LEFT_TO_RIGHT

Cardiolipin synthase (CMP-forming)
type: ProteinReference
xref: Reference/UniProt Q07560

CL(10:0/16:1(9Z)/18:1(11Z)/28:1(9Z))
type: SmallMolecule
entity reference: CL(10:0/16:1(9Z)/18:1(11Z)/28:1(9Z))

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

Reference/UniProt P53264
type: UnificationXref
id: P53264
db: UniProt

Reference/ChemSpider 5901
type: UnificationXref
id: 5901
db: ChemSpider

Reference/ChEBI CHEBI 17962
type: UnificationXref
id: CHEBI:17962
db: ChEBI

Reference/UniProt P33333
type: UnificationXref
id: P33333
db: UniProt

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

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

Reference/KEGG Compound C00055
type: UnificationXref
id: C00055
db: KEGG Compound

Compound/PW C055665/Stoichiometry/1.0
type: Stoichiometry
physical entity: PC(10:0/10:0)
stoichiometric coefficient: 1.0

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

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

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

Reference/KEGG Compound C00063
type: UnificationXref
id: C00063
db: KEGG Compound

Reference/ChEBI CHEBI 30813
type: UnificationXref
id: CHEBI:30813
db: ChEBI

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

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

Reference/SMPDB SMP0004745
type: UnificationXref
id: SMP0004745
db: SMPDB

Reference/UniProt P38221
type: UnificationXref
id: P38221
db: UniProt

ChemicalStructure/PW C000391
type: ChemicalStructure
structure format: SMILES
structure data: CCCCCCCCCC(O)=O

Reference/UniProt P36165
type: UnificationXref
id: P36165
db: UniProt

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

Reference/ChemSpider 2863
type: UnificationXref
id: 2863
db: ChemSpider

PA(10:0/16:1(9Z))
type: SmallMolecule
cellular location: Endoplasmic Reticulum Membrane
entity reference: PA(10:0/16:1(9Z))

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

Reference/CAS 65-47-4
type: UnificationXref
id: 65-47-4
db: CAS

PG(10:0/16:1(9Z))
type: SmallMolecule
entity reference: PG(10:0/16:1(9Z))

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

Compound/PW C002742/Stoichiometry/1.0
type: Stoichiometry
physical entity: Decanoyl-CoA
stoichiometric coefficient: 1.0

ChemicalStructure/PW C042689
type: ChemicalStructure
structure format: SMILES

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

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

Reference/ChEBI CHEBI 37393
type: UnificationXref
id: CHEBI:37393
db: ChEBI

Lysophosphatidylcholine acyltransferase
type: Protein
entity reference: Lysophosphatidylcholine acyltransferase

Reference/UniProt P32784
type: UnificationXref
id: P32784
db: UniProt

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

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

Compound/PW C000391/Stoichiometry/1.0
type: Stoichiometry
physical entity: Capric acid
stoichiometric coefficient: 1.0

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

MLCL(0:0/16:1(9Z)/18:1(11Z)/28:1(9Z))
type: SmallMolecule
entity reference: MLCL(0:0/16:1(9Z)/18:1(11Z)/28:1(9Z))

Compound/PW C105082/Stoichiometry/1.0
type: Stoichiometry
physical entity: PG(10:0/16:1(9Z))
stoichiometric coefficient: 1.0

Reference/UniProt P25578
type: UnificationXref
id: P25578
db: UniProt

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

Reference/ChEBI CHEBI 17677
type: UnificationXref
id: CHEBI:17677
db: ChEBI

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

Reference/UniProt Q92328
type: UnificationXref
id: Q92328
db: UniProt

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

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

Reference/PubChem-compound 6176
type: UnificationXref
id: 6176
db: PubChem-compound

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

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/UniProt O60200
type: UnificationXref
id: O60200
db: UniProt

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

Reference/PubChem-compound 644102
type: UnificationXref
id: 644102
db: PubChem-compound

Reference/TAXONOMY 4932
type: UnificationXref
id: 4932
db: TAXONOMY

Reference/ChemSpider 5941
type: UnificationXref
id: 5941
db: ChemSpider

LysoPA(10:0/0:0)
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 16975
xref: Reference/KEGG Compound C00681
xref: Reference/BioCyc ACYL-SN-GLYCEROL-3P
chemical formula: C13H27O7P
molecular weight: 326.14944
structure: ChemicalStructure/PW C055362

Reference/UniProt Q08548
type: UnificationXref
id: Q08548
db: UniProt

Reference/UniProt Q00055
type: UnificationXref
id: Q00055
db: UniProt

Compound/PW C042689/Stoichiometry/1.0
type: Stoichiometry
physical entity: CDP-DG(10:0/16:1(9Z))
stoichiometric coefficient: 1.0

ChemicalStructure/PW C055535
type: ChemicalStructure
structure format: SMILES

Reference/PubChem-compound 2969
type: UnificationXref
id: 2969
db: PubChem-compound

ChemicalStructure/PW C105051
type: ChemicalStructure
structure format: SMILES

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/HMDB HMDB0000511
type: UnificationXref
id: HMDB0000511
db: HMDB

Reference/UniProt P41800
type: UnificationXref
id: P41800
db: UniProt

Glycerol-3-phosphate dehydrogenase GPD2
type: ProteinReference
xref: Reference/UniProt P41911

ChemicalStructure/PW C108327
type: ChemicalStructure
structure format: SMILES
structure data: [H][C@@](O)(COC(=O)CCCCCCCCC)COP([O-])(=O)OCC[N+](C)(C)C

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

Glycerol-3-phosphate dehydrogenase
type: ProteinReference
xref: Reference/UniProt Q00055

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

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

Lysophosphatidic acid:oleoyl-CoA acyltransferase 1
type: Protein
entity reference: Lysophosphatidic acid:oleoyl-CoA acyltransferase 1

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

LysoPA(10:0/0:0)
type: SmallMolecule
entity reference: LysoPA(10:0/0:0)

Lysophosphatidate acyltransferase
type: Complex
component: Lysophosphatidic acid:oleoyl-CoA acyltransferase 1
component: Acyl-CoA:lyso-phospholipid acyltransferase
component: Lipase 4
component: Probable 1-acyl-sn-glycerol-3-phosphate acyltransferase
component: Lipase 5

Acyl-CoA:lyso-phospholipid acyltransferase
type: Protein
entity reference: Acyl-CoA:lyso-phospholipid acyltransferase

Lipase 4
type: Protein
entity reference: Lipase 4

Glycerol-3-phosphate O-acyltransferase
type: Complex
component: Glycerol-3-phosphate O-acyltransferase 2
component: Glycerol-3-phosphate O-acyltransferase 1

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

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

Lipase 5
type: Protein
entity reference: Lipase 5

Reference/KEGG Compound C04230
type: UnificationXref
id: C04230
db: KEGG Compound

ChemicalStructure/PW C055665
type: ChemicalStructure
structure format: SMILES
structure data: [H][C@@](COC(=O)CCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCC

Reference/HMDB HMDB0000082
type: UnificationXref
id: HMDB0000082
db: HMDB

ChemicalStructure/PW C045630
type: ChemicalStructure
structure format: SMILES

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

Cardiolipin-specific deacylase 1, mitochondrial
type: Protein
entity reference: Cardiolipin-specific deacylase 1, mitochondrial

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

Reference/UniProt P53230
type: UnificationXref
id: P53230
db: UniProt