AMP-binding protein
type: Protein
entity reference: AMP-binding protein

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

Acetyl-CoA
type: SmallMoleculeReference
xref: Reference/BioCyc ACETYL-COA
xref: Reference/PubChem-compound 444493
xref: Reference/HMDB HMDB0001206
xref: Reference/ChemSpider 392413
xref: Reference/CAS 72-89-9
xref: Reference/ChEBI CHEBI 15351
xref: Reference/KEGG Compound C00024
chemical formula: C23H38N7O17P3S
molecular weight: 809.1258
structure: ChemicalStructure/PW C000940

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

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

ChemicalStructure/PW C000721
type: ChemicalStructure
structure format: SMILES

Compound/Generic161/Stoichiometry/1.0
type: Stoichiometry
physical entity: an oxidized electron-transfer flavoprotein
stoichiometric coefficient: 1.0

4.2.1.17
type: BiochemicalReaction
participant stoichiometry: Compound/PW C008081/Stoichiometry/1.0
participant stoichiometry: Compound/PW C002796/Stoichiometry/1.0
right: (2E)-Octadecenoyl-CoA
spontaneous: false
EC number: 4.2.1.17
left: 3-hydroxyoctadecanoyl-CoA
name: 3-hydroxyoctadecanoyl-CoA → (2E)-Octadecenoyl-CoA
conversion direction: LEFT_TO_RIGHT

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

Reduced electron-transfer flavoprotein
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 5086

ChemicalStructure/PW C001144
type: ChemicalStructure
structure format: SMILES

Reaction550667
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000661/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000032/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000414/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000871/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001099/Stoichiometry/1.0
right: Stearoyl-CoA
right: Adenosine monophosphate
spontaneous: false
left: Coenzyme A
left: Stearic acid
left: Adenosine triphosphate
name: Adenosine triphosphate + Coenzyme A + Stearic acid → Adenosine monophosphate + Stearoyl-CoA
conversion direction: LEFT_TO_RIGHT

NADH
type: SmallMolecule
entity reference: NADH

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

Reaction550668
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001099/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001031/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000940/Stoichiometry/1.0
participant stoichiometry: Compound/PW C002775/Stoichiometry/1.0
right: Palmitoyl-CoA
right: Acetyl-CoA
spontaneous: false
left: Coenzyme A
left: 3-oxooctadecanoyl-CoA
name: 3-oxooctadecanoyl-CoA + Coenzyme A → Acetyl-CoA + Palmitoyl-CoA
conversion direction: LEFT_TO_RIGHT

Reaction550665
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C008081/Stoichiometry/1.0
participant stoichiometry: Compound/PW C002796/Stoichiometry/1.0
right: 3-hydroxyoctadecanoyl-CoA
right: Water
spontaneous: false
left: (2E)-Octadecenoyl-CoA
name: (2E)-Octadecenoyl-CoA → 3-hydroxyoctadecanoyl-CoA + Water
conversion direction: LEFT_TO_RIGHT

Water
type: SmallMolecule
entity reference: Water

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

Reaction550666
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000721/Stoichiometry/1.0
participant stoichiometry: Compound/PW C008081/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001144/Stoichiometry/1.0
participant stoichiometry: Compound/PW C002775/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: NADH
right: Hydrogen Ion
right: 3-oxooctadecanoyl-CoA
spontaneous: false
left: 3-hydroxyoctadecanoyl-CoA
left: NAD
name: 3-hydroxyoctadecanoyl-CoA + NAD → 3-oxooctadecanoyl-CoA + Hydrogen Ion + NADH
conversion direction: LEFT_TO_RIGHT

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

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

Reference/KEGG Compound C16216
type: UnificationXref
id: C16216
db: KEGG Compound

Reference/BioCyc STEARIC ACID
type: UnificationXref
id: STEARIC_ACID
db: BioCyc

Reference/KEGG Compound C16217
type: UnificationXref
id: C16217
db: KEGG Compound

Reference/KEGG Compound C16218
type: UnificationXref
id: C16218
db: KEGG Compound

Adenosine monophosphate
type: SmallMoleculeReference
xref: Reference/CAS 61-19-8
xref: Reference/ChemSpider 5858
xref: Reference/HMDB HMDB0000045
xref: Reference/BioCyc AMP
xref: Reference/ChEBI CHEBI 16027
xref: Reference/PubChem-compound 6083
xref: Reference/KEGG Compound C00020
chemical formula: C10H14N5O7P
molecular weight: 347.06308
structure: ChemicalStructure/PW C000032

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

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

Reference/PubChem-compound 53481517
type: UnificationXref
id: 53481517
db: PubChem-compound

Reference/ChEBI CHEBI 16027
type: UnificationXref
id: CHEBI:16027
db: ChEBI

Fatty Acid Oxidation (Steareate)
type: Pathway
pathway order: PathwayEnzymeReaction/5441502
pathway order: PathwayEnzymeReaction/5441501
pathway order: PathwayEnzymeReaction/5441503
pathway order: PathwaySubPathway/366029
pathway order: PathwayEnzymeReaction/5441498
pathway order: PathwayEnzymeReaction/5441497
pathway order: PathwayEnzymeReaction/5441500
pathway order: PathwayEnzymeReaction/5441499
pathway component: ReactionCatalysis543586
pathway component: ReactionCatalysis543582
pathway component: ReactionCatalysis543583
pathway component: ReactionCatalysis543584
pathway component: ReactionCatalysis543585
pathway component: 4.2.1.17
pathway component: Reaction550667
pathway component: Reaction550668
pathway component: Reaction550665
pathway component: Reaction550666
pathway component: Reaction3801
pathway component: ReactionCatalysis543581
pathway component: Fatty Acid Oxidation (Palmitate)
xref: Reference/SMPDB SMP0376390
xref: Reference/PathWhiz PW382324
organism: Alistipes indistinctus YIT 12060

Reference/PathWhiz PW001023
type: UnificationXref
id: PW001023
db: PathWhiz

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

Reference/PubChem-compound 5281
type: UnificationXref
id: 5281
db: PubChem-compound

NAD
type: SmallMolecule
entity reference: NAD

Reference/KEGG Compound C01530
type: UnificationXref
id: C01530
db: KEGG Compound

Reference/HMDB HMDB0000538
type: UnificationXref
id: HMDB0000538
db: HMDB

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

Reference/CAS 72-89-9
type: UnificationXref
id: 72-89-9
db: CAS

Reference/ChemSpider 388366
type: UnificationXref
id: 388366
db: ChemSpider

Compound/PW C002796/Stoichiometry/1.0
type: Stoichiometry
physical entity: (2E)-Octadecenoyl-CoA
stoichiometric coefficient: 1.0

Reference/ChEBI CHEBI 50583
type: UnificationXref
id: CHEBI:50583
db: ChEBI

Compound/PW C000661/Stoichiometry/1.0
type: Stoichiometry
physical entity: Stearic acid
stoichiometric coefficient: 1.0

Coenzyme A
type: SmallMolecule
entity reference: Coenzyme A

Reference/HMDB HMDB0006529
type: UnificationXref
id: HMDB0006529
db: HMDB

Compound/PW C000414/Stoichiometry/1.0
type: Stoichiometry
physical entity: Adenosine triphosphate
stoichiometric coefficient: 1.0

Reference/HMDB HMDB0001114
type: UnificationXref
id: HMDB0001114
db: HMDB

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

ChemicalStructure/PW C001031
type: ChemicalStructure
structure format: SMILES

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

4.2.1.17
type: BiochemicalReaction
participant stoichiometry: Compound/PW C008081/Stoichiometry/1.0
participant stoichiometry: Compound/PW C002796/Stoichiometry/1.0
right: (2E)-Octadecenoyl-CoA
spontaneous: false
EC number: 4.2.1.17
left: 3-hydroxyoctadecanoyl-CoA
name: 3-hydroxyoctadecanoyl-CoA → (2E)-Octadecenoyl-CoA
conversion direction: LEFT_TO_RIGHT

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

Cytoplasm
type: CellularLocationVocabulary
xref: Reference/GENE ONTOLOGY GO 0005737

Compound/PW C008081/Stoichiometry/1.0
type: Stoichiometry
physical entity: 3-hydroxyoctadecanoyl-CoA
stoichiometric coefficient: 1.0

FadJ component of anaerobic fatty acid oxidation complex
type: Complex
component stoichiometry: Protein/29064/Stoichiometry/2.0
component: Unknown

Unknown
type: ProteinReference

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

Reference/ChEBI CHEBI 15541
type: UnificationXref
id: CHEBI:15541
db: ChEBI

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

Reference/ChEBI CHEBI 15422
type: UnificationXref
id: CHEBI:15422
db: ChEBI

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

Compound/PW C000940/Stoichiometry/1.0
type: Stoichiometry
physical entity: Acetyl-CoA
stoichiometric coefficient: 1.0

Reference/ChemSpider 5742
type: UnificationXref
id: 5742
db: ChemSpider

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

ChemicalStructure/PW C000940
type: ChemicalStructure
structure format: SMILES

Palmitoyl-CoA
type: SmallMolecule
cellular location: Cytoplasm
entity reference: Palmitoyl-CoA
name: SubPathwayInput

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

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

Reference/HMDB HMDB0000827
type: UnificationXref
id: HMDB0000827
db: HMDB

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

Reference/CAS 61-19-8
type: UnificationXref
id: 61-19-8
db: CAS

ChemicalStructure/PW C000032
type: ChemicalStructure
structure format: SMILES

(2E)-Octadecenoyl-CoA
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0006529
xref: Reference/PubChem-compound 53477850
xref: Reference/KEGG Compound C16218
chemical formula: C39H68N7O17P3S
molecular weight: 1031.3605
structure: ChemicalStructure/PW C002796

Adenosine monophosphate
type: SmallMolecule
entity reference: Adenosine monophosphate

Reference/HMDB HMDB0006498
type: UnificationXref
id: HMDB0006498
db: HMDB

Compound/Generic70/Stoichiometry/1.0
type: Stoichiometry
physical entity: Reduced electron-transfer flavoprotein
stoichiometric coefficient: 1.0

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

Reference/ChemSpider 5858
type: UnificationXref
id: 5858
db: ChemSpider

Adenosine triphosphate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 15422
xref: Reference/PubChem-compound 5957
xref: Reference/HMDB HMDB0000538
xref: Reference/CAS 56-65-5
xref: Reference/ChemSpider 5742
xref: Reference/BioCyc ATP
xref: Reference/KEGG Compound C00002
chemical formula: C10H16N5O13P3
molecular weight: 506.99576
structure: ChemicalStructure/PW C000414

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

Acetyl-CoA
type: SmallMolecule
entity reference: Acetyl-CoA

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

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

ChemicalStructure/PW C001099
type: ChemicalStructure
structure format: SMILES

Reference/HMDB HMDB0000045
type: UnificationXref
id: HMDB0000045
db: HMDB

Stearic acid
type: SmallMolecule
entity reference: Stearic acid

Stearic acid
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 28842
xref: Reference/PubChem-compound 5281
xref: Reference/ChemSpider 5091
xref: Reference/KEGG Compound C01530
xref: Reference/BioCyc STEARIC ACID
xref: Reference/HMDB HMDB0000827
xref: Reference/CAS 57-11-4
chemical formula: C18H36O2
molecular weight: 284.27155
structure: ChemicalStructure/PW C000661

Fatty Acid Oxidation (Palmitate)
type: Pathway
pathway order: SubPathwayInteractionSteps/SubPathway366029
pathway component: SubPathwayInteraction366029
xref: Reference/PathWhiz PW001023
xref: Reference/SMPDB SMP0001039
name: SubPathway

Reference/PubChem-compound 22833663
type: UnificationXref
id: 22833663
db: PubChem-compound

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

Compound/PW C000032/Stoichiometry/1.0
type: Stoichiometry
physical entity: Adenosine monophosphate
stoichiometric coefficient: 1.0

Hydrogen Ion
type: SmallMolecule
entity reference: Hydrogen Ion

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

Reference/ChemSpider 392413
type: UnificationXref
id: 392413
db: ChemSpider

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

Reference/ChEBI CHEBI 5086
type: UnificationXref
id: CHEBI:5086
db: ChEBI

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

Adenosine triphosphate
type: SmallMolecule
entity reference: Adenosine triphosphate

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

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

ChemicalStructure/PW C002796
type: ChemicalStructure
structure format: SMILES

Reference/ChEBI CHEBI 28842
type: UnificationXref
id: CHEBI:28842
db: ChEBI

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

(2E)-Octadecenoyl-CoA
type: SmallMolecule
entity reference: (2E)-Octadecenoyl-CoA

Reference/ChemSpider 17216373
type: UnificationXref
id: 17216373
db: ChemSpider

3-oxooctadecanoyl-CoA
type: SmallMoleculeReference
xref: Reference/ChemSpider 17216373
xref: Reference/HMDB HMDB0006498
xref: Reference/KEGG Compound C16216
xref: Reference/CAS 86370-20-9
xref: Reference/PubChem-compound 22833663
chemical formula: C39H68N7O18P3S
molecular weight: 1047.3555
structure: ChemicalStructure/PW C002775

Reference/ChemSpider 5091
type: UnificationXref
id: 5091
db: ChemSpider

Reference/SMPDB SMP0376390
type: UnificationXref
id: SMP0376390
db: SMPDB

Stearoyl-CoA
type: SmallMoleculeReference
xref: Reference/CAS 362-66-3
xref: Reference/ChEBI CHEBI 15541
xref: Reference/HMDB HMDB0001114
xref: Reference/KEGG Compound C00412
xref: Reference/BioCyc STEAROYL-COA
xref: Reference/ChemSpider 388366
xref: Reference/PubChem-compound 439229
chemical formula: C39H70N7O17P3S
molecular weight: 1033.3762
structure: ChemicalStructure/PW C000871

Reduced electron-transfer flavoprotein
type: SmallMolecule
entity reference: Reduced electron-transfer flavoprotein

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

Protein/29064/Stoichiometry/2.0
type: Stoichiometry
physical entity: Unknown
stoichiometric coefficient: 2.0

Reference/CAS 57-11-4
type: UnificationXref
id: 57-11-4
db: CAS

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

Reference/PubChem-compound 53477850
type: UnificationXref
id: 53477850
db: PubChem-compound

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

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

3-hydroxyoctadecanoyl-CoA
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 50583
xref: Reference/CAS 42578-91-6
xref: Reference/PubChem-compound 53481517
xref: Reference/HMDB HMDB0012715
xref: Reference/KEGG Compound C16217
chemical formula: C39H70N7O18P3S
molecular weight: 1049.3711
structure: ChemicalStructure/PW C008081

Unknown
type: Protein
entity reference: Unknown

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

ChemicalStructure/PW C000414
type: ChemicalStructure
structure format: SMILES

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

Reference/KEGG Compound C00002
type: UnificationXref
id: C00002
db: KEGG Compound

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

ChemicalStructure/PW C000661
type: ChemicalStructure
structure format: SMILES
structure data: CCCCCCCCCCCCCCCCCC(O)=O

Reference/HMDB HMDB0012715
type: UnificationXref
id: HMDB0012715
db: HMDB

Reference/CAS 86370-20-9
type: UnificationXref
id: 86370-20-9
db: CAS

an oxidized electron-transfer flavoprotein
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 5086

Compound/PW C002775/Stoichiometry/1.0
type: Stoichiometry
physical entity: 3-oxooctadecanoyl-CoA
stoichiometric coefficient: 1.0

Reference/PubChem-compound 439229
type: UnificationXref
id: 439229
db: PubChem-compound

ReactionCatalysis543586
type: Catalysis
controller: Unknown
controlled: 4.2.1.17
control type: ACTIVATION

Reference/CAS 362-66-3
type: UnificationXref
id: 362-66-3
db: CAS

3-hydroxyoctadecanoyl-CoA
type: SmallMolecule
entity reference: 3-hydroxyoctadecanoyl-CoA

ReactionCatalysis543582
type: Catalysis
controller: Unknown
controlled: Reaction550666
control type: ACTIVATION

Reference/PubChem-compound 444493
type: UnificationXref
id: 444493
db: PubChem-compound

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

ReactionCatalysis543583
type: Catalysis
controller: AMP-binding protein
controlled: Reaction550667
control type: ACTIVATION

Reference/PubChem-compound 6083
type: UnificationXref
id: 6083
db: PubChem-compound

ReactionCatalysis543584
type: Catalysis
controller: Unknown
controlled: Reaction550668
control type: ACTIVATION

ReactionCatalysis543585
type: Catalysis
controller: FadJ component of anaerobic fatty acid oxidation complex
controlled: 4.2.1.17
control type: ACTIVATION

Reference/SMPDB SMP0001039
type: UnificationXref
id: SMP0001039
db: SMPDB

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

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

Reference/KEGG Compound C00412
type: UnificationXref
id: C00412
db: KEGG Compound

3-oxooctadecanoyl-CoA
type: SmallMolecule
entity reference: 3-oxooctadecanoyl-CoA

ChemicalStructure/PW C002775
type: ChemicalStructure
structure format: SMILES

an oxidized electron-transfer flavoprotein
type: SmallMolecule
entity reference: an oxidized electron-transfer flavoprotein

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

Stearoyl-CoA
type: SmallMolecule
entity reference: Stearoyl-CoA

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

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

ChemicalStructure/PW C000871
type: ChemicalStructure
structure format: SMILES

Reference/PubChem-compound 5957
type: UnificationXref
id: 5957
db: PubChem-compound

Reference/HMDB HMDB0001206
type: UnificationXref
id: HMDB0001206
db: HMDB

ReactionCatalysis543581
type: Catalysis
controller: Unknown
controlled: Reaction550665
control type: ACTIVATION

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

Reference/TAXONOMY 742725
type: UnificationXref
id: 742725
db: TAXONOMY

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

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

Compound/PW C000871/Stoichiometry/1.0
type: Stoichiometry
physical entity: Stearoyl-CoA
stoichiometric coefficient: 1.0

ChemicalStructure/PW C008081
type: ChemicalStructure
structure format: SMILES

SubPathwayInteraction366029
type: Interaction
name: SubPathwayReaction
name: SubPathway366029Reaction
participant: Palmitoyl-CoA

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

Reference/PathWhiz PW382324
type: UnificationXref
id: PW382324
db: PathWhiz

Reference/CAS 56-65-5
type: UnificationXref
id: 56-65-5
db: CAS

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

Reference/KEGG Compound C00020
type: UnificationXref
id: C00020
db: KEGG Compound

Reference/ChEBI CHEBI 15351
type: UnificationXref
id: CHEBI:15351
db: ChEBI

Reference/UniProt G5HAS1
type: UnificationXref
id: G5HAS1
db: UniProt

Reference/KEGG Compound C00024
type: UnificationXref
id: C00024
db: KEGG Compound

Palmitoyl-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/CAS 42578-91-6
type: UnificationXref
id: 42578-91-6
db: CAS

Alistipes indistinctus YIT 12060
type: BioSource
xref: Reference/TAXONOMY 742725

Reference/GENE ONTOLOGY GO 0005737
type: UnificationXref
id: GO:0005737
db: GENE ONTOLOGY

Palmitoyl-CoA
type: SmallMolecule
entity reference: Palmitoyl-CoA

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

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

Reaction3801
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000871/Stoichiometry/1.0
participant stoichiometry: Compound/Generic70/Stoichiometry/1.0
participant stoichiometry: Compound/Generic161/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C002796/Stoichiometry/1.0
right: (2E)-Octadecenoyl-CoA
right: Reduced electron-transfer flavoprotein
spontaneous: true
left: an oxidized electron-transfer flavoprotein
left: Stearoyl-CoA
left: Hydrogen Ion
name: Hydrogen Ion + Stearoyl-CoA + an oxidized electron-transfer flavoprotein → (2E)-Octadecenoyl-CoA + Reduced electron-transfer flavoprotein
conversion direction: LEFT_TO_RIGHT

AMP-binding protein
type: ProteinReference
xref: Reference/UniProt G5HAS1