Reference/ChEBI CHEBI 16136
type: UnificationXref
id: CHEBI:16136
db: ChEBI

cystathionine beta-lyase
type: Protein
entity reference: cystathionine beta-lyase

Reference/CAS 454-29-5
type: UnificationXref
id: 454-29-5
db: CAS

cystathionine beta-lyase subunit 2
type: Protein
entity reference: cystathionine beta-lyase subunit 2

cystathionine beta-synthase
type: Protein
entity reference: cystathionine beta-synthase

Reference/ChemSpider 17215925
type: UnificationXref
id: 17215925
db: ChemSpider

Reference/PubChem-compound 6022
type: UnificationXref
id: 6022
db: PubChem-compound

Acetic acid
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 15366
xref: Reference/BioCyc ACET
xref: Reference/CAS 64-19-7
xref: Reference/KEGG Compound C00033
xref: Reference/ChemSpider 171
xref: Reference/HMDB HMDB0000042
xref: Reference/PubChem-compound 176
chemical formula: C2H4O2
molecular weight: 60.02113
structure: ChemicalStructure/PW C000029

Hydrogen sulfide
type: SmallMolecule
entity reference: Hydrogen sulfide

homoserine O-trans-acetylase
type: Protein
entity reference: homoserine O-trans-acetylase

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

O-acetylhomoserine (thiol)-lyase
type: Protein
entity reference: O-acetylhomoserine (thiol)-lyase

Reaction2903
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040928/Stoichiometry/1.0
participant stoichiometry: Compound/PW C022608/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000164/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Ammonium
right: Pyruvic acid
spontaneous: true
left: Water
left: 2-iminopropanoate
left: Hydrogen Ion
name: 2-iminopropanoate + Hydrogen Ion + Water → Ammonium + Pyruvic acid
conversion direction: LEFT_TO_RIGHT

ChemicalStructure/PW C000448
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CS)C(O)=O

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

Reference/CAS 22138-53-0
type: UnificationXref
id: 22138-53-0
db: CAS

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

Reference/KEGG Compound C05330
type: UnificationXref
id: C05330
db: KEGG Compound

ChemicalStructure/PW C000570
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CCO)C(O)=O

Reference/PubChem-compound 18779926
type: UnificationXref
id: 18779926
db: PubChem-compound

Reference/CAS 64-19-7
type: UnificationXref
id: 64-19-7
db: CAS

Reference/ChemSpider 57
type: UnificationXref
id: 57
db: ChemSpider

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

Reference/UniProt P13663
type: UnificationXref
id: P13663
db: UniProt

Reference/ChEBI CHEBI 58020
type: UnificationXref
id: CHEBI:58020
db: ChEBI

Reaction6146
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040928/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040921/Stoichiometry/1.0
right: 2-iminopropanoate
spontaneous: true
left: 2-aminoprop-2-enoate
name: 2-aminoprop-2-enoate → 2-iminopropanoate
conversion direction: LEFT_TO_RIGHT

Acetylhomoserine
type: SmallMolecule
entity reference: Acetylhomoserine

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

Reference/HMDB HMDB0000099
type: UnificationXref
id: HMDB0000099
db: HMDB

Reference/ChEBI CHEBI 17115
type: UnificationXref
id: CHEBI:17115
db: ChEBI

Reference/UniProt P06106
type: UnificationXref
id: P06106
db: UniProt

Reference/ChemSpider 809
type: UnificationXref
id: 809
db: ChemSpider

Reference/KEGG Compound C00441
type: UnificationXref
id: C00441
db: KEGG Compound

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

Reference/ChEBI CHEBI 17230
type: UnificationXref
id: CHEBI:17230
db: ChEBI

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

SubPathwayInteraction111231
type: Interaction
name: SubPathwayReaction
name: SubPathway111231Reaction

Ammonium
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0041827
xref: Reference/CAS 14798-03-9
xref: Reference/PubChem-compound 16741146
xref: Reference/KEGG Compound C01342
xref: Reference/ChEBI CHEBI 28938
xref: Reference/ChemSpider 218
chemical formula: H4N
molecular weight: 18.034374
structure: ChemicalStructure/PW C022608

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

ReactionCatalysis6229
type: Catalysis
controller: cystathionine gamma-lyase
controlled: 4.4.1.1
control type: ACTIVATION

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

Pyruvic acid
type: SmallMolecule
entity reference: Pyruvic acid

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

Pyruvic acid
type: SmallMoleculeReference
xref: Reference/PubChem-compound 1060
xref: Reference/HMDB HMDB0000243
xref: Reference/CAS 127-17-3
xref: Reference/BioCyc PYRUVATE
xref: Reference/KEGG Compound C00022
xref: Reference/ChEBI CHEBI 32816
xref: Reference/ChemSpider 1031
chemical formula: C3H4O3
molecular weight: 88.016045
structure: ChemicalStructure/PW C000164

ReactionCatalysis6228
type: Catalysis
controller: cystathionine beta-synthase
controlled: 4.2.1.22
control type: ACTIVATION

Reference/PubChem-compound 58
type: UnificationXref
id: 58
db: PubChem-compound

ReactionCatalysis6227
type: Catalysis
controller: cystathionine beta-lyase
controlled: 4.4.1.8
control type: ACTIVATION

ReactionCatalysis6226
type: Catalysis
controller: O-acetylhomoserine (thiol)-lyase
controlled: 2.5.1.49,2.5.1.47
control type: ACTIVATION

Reference/PubChem-compound 49791978
type: UnificationXref
id: 49791978
db: PubChem-compound

ReactionCatalysis6225
type: Catalysis
controller: homoserine O-trans-acetylase
controlled: 2.3.1.31
control type: ACTIVATION

Reference/CAS 53-59-8
type: UnificationXref
id: 53-59-8
db: CAS

ReactionCatalysis6231
type: Catalysis
controller: aspartic beta semi-aldehyde dehydrogenase
controlled: 1.2.1.11
control type: ACTIVATION

ChemicalStructure/PW C040921
type: ChemicalStructure
structure format: SMILES
structure data: NC(=C)C([O-])=O

ReactionCatalysis6230
type: Catalysis
controller: Homoserine dehydrogenase
controlled: 1.1.1.3
control type: ACTIVATION

Compound/PW C001034/Stoichiometry/1.0
type: Stoichiometry
physical entity: Adenosine diphosphate
stoichiometric coefficient: 1.0

Reference/ChemSpider 5745
type: UnificationXref
id: 5745
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

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

ChemicalStructure/PW C040928
type: ChemicalStructure
structure format: SMILES
structure data: CC(=N)C([O-])=O

Reference/ChEBI CHEBI 17561
type: UnificationXref
id: CHEBI:17561
db: ChEBI

Reference/ChEBI CHEBI 16474
type: UnificationXref
id: CHEBI:16474
db: ChEBI

Reference/UniProt P43623
type: UnificationXref
id: P43623
db: UniProt

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

Compound/PW C000067/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Cystathionine
stoichiometric coefficient: 1.0

ReactionCatalysis6233
type: Catalysis
controller: cystathionine gamma-lyase
controlled: Reaction6305
control type: ACTIVATION

Reference/ChemSpider 391
type: UnificationXref
id: 391
db: ChemSpider

ReactionCatalysis6232
type: Catalysis
controller: aspartokinase
controlled: 2.7.2.4
control type: ACTIVATION

Reference/ChemSpider 5736
type: UnificationXref
id: 5736
db: ChemSpider

Compound/PW C000448/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Cysteine
stoichiometric coefficient: 1.0

Reference/KEGG Compound C00109
type: UnificationXref
id: C00109
db: KEGG Compound

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

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

NADPH
type: SmallMolecule
entity reference: NADPH

Reference/PubChem-compound 5862
type: UnificationXref
id: 5862
db: PubChem-compound

Reference/UniProt P10869
type: UnificationXref
id: P10869
db: UniProt

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

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

Acetic acid
type: SmallMolecule
entity reference: Acetic acid

Saccharomyces cerevisiae
type: BioSource
xref: Reference/TAXONOMY 4932

ChemicalStructure/PW C001099
type: ChemicalStructure
structure format: SMILES

Reference/CAS 600-18-0
type: UnificationXref
id: 600-18-0
db: CAS

NADP
type: SmallMolecule
entity reference: NADP

NADPH
type: SmallMoleculeReference
xref: Reference/CAS 53-57-6
xref: Reference/HMDB HMDB0000221
xref: Reference/PubChem-compound 22833512
xref: Reference/BioCyc NADPH
xref: Reference/ChemSpider 17215925
xref: Reference/KEGG Compound C00005
xref: Reference/ChEBI CHEBI 16474
chemical formula: C21H30N7O17P3
molecular weight: 745.0911
structure: ChemicalStructure/PW C000146

NADP
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00006
xref: Reference/CAS 53-59-8
xref: Reference/BioCyc NAD(P)
xref: Reference/HMDB HMDB0000217
xref: Reference/ChEBI CHEBI 18009
xref: Reference/PubChem-compound 5886
xref: Reference/ChemSpider 5675
chemical formula: C21H28N7O17P3
molecular weight: 743.07544
structure: ChemicalStructure/PW C000143

Reference/HMDB HMDB0003276
type: UnificationXref
id: HMDB0003276
db: HMDB

Compound/PW C000146/Stoichiometry/1.0
type: Stoichiometry
physical entity: NADPH
stoichiometric coefficient: 1.0

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

Ammonium
type: SmallMolecule
entity reference: Ammonium

Hydrogen Ion
type: SmallMolecule
entity reference: Hydrogen Ion

2-aminoprop-2-enoate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 58020
chemical formula: C3H4NO2
molecular weight: 86.02475
structure: ChemicalStructure/PW C040921

Reference/CAS 672-15-1
type: UnificationXref
id: 672-15-1
db: CAS

Reference/ChemSpider 218
type: UnificationXref
id: 218
db: ChemSpider

Adenosine triphosphate
type: SmallMolecule
entity reference: Adenosine triphosphate

2-iminopropanoate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 77456
chemical formula: C3H4NO2
molecular weight: 86.02475
structure: ChemicalStructure/PW C040928

Reference/HMDB HMDB0000574
type: UnificationXref
id: HMDB0000574
db: HMDB

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

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

Acetylhomoserine
type: SmallMoleculeReference
xref: Reference/CAS 7540-67-2
xref: Reference/PubChem-compound 528
xref: Reference/HMDB HMDB0029423
xref: Reference/ChEBI CHEBI 7671
xref: Reference/ChemSpider 513
chemical formula: C6H11NO4
molecular weight: 161.0688
structure: ChemicalStructure/PW C010666

Reference/HMDB HMDB0000217
type: UnificationXref
id: HMDB0000217
db: HMDB

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

Reference/KEGG Compound C00008
type: UnificationXref
id: C00008
db: KEGG Compound

Reference/KEGG Compound C00006
type: UnificationXref
id: C00006
db: KEGG Compound

Reference/ChEBI CHEBI 18009
type: UnificationXref
id: CHEBI:18009
db: ChEBI

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

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

Reference/KEGG Compound C00005
type: UnificationXref
id: C00005
db: KEGG Compound

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

Reference/BioCyc 2-OXOBUTANOATE
type: UnificationXref
id: 2-OXOBUTANOATE
db: BioCyc

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

Reference/ChemSpider 1031
type: UnificationXref
id: 1031
db: ChemSpider

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

ChemicalStructure/PW C000143
type: ChemicalStructure
structure format: SMILES

Compound/PW C040928/Stoichiometry/1.0
type: Stoichiometry
physical entity: 2-iminopropanoate
stoichiometric coefficient: 1.0

Reference/HMDB HMDB0000221
type: UnificationXref
id: HMDB0000221
db: HMDB

Compound/PW C010666/Stoichiometry/1.0
type: Stoichiometry
physical entity: Acetylhomoserine
stoichiometric coefficient: 1.0

ChemicalStructure/PW C000146
type: ChemicalStructure
structure format: SMILES

Reference/KEGG Compound C03082
type: UnificationXref
id: C03082
db: KEGG Compound

2.3.1.31
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000570/Stoichiometry/1.0
participant stoichiometry: Compound/PW C010666/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001099/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000940/Stoichiometry/1.0
right: Coenzyme A
right: Acetylhomoserine
spontaneous: false
EC number: 2.3.1.31
left: L-Homoserine
left: Acetyl-CoA
name: Acetyl-CoA + L-Homoserine → Acetylhomoserine + Coenzyme A
conversion direction: LEFT_TO_RIGHT

cystathionine beta-lyase
type: ProteinReference
xref: Reference/UniProt P43623

O-acetylhomoserine (thiol)-lyase
type: ProteinReference
xref: Reference/UniProt P06106

2.5.1.49,2.5.1.47
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000029/Stoichiometry/1.0
participant stoichiometry: Compound/PW C010666/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001827/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000590/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Homocysteine
right: Hydrogen Ion
right: Acetic acid
spontaneous: false
EC number: 2.5.1.49,2.5.1.47
left: Hydrogen sulfide
left: Acetylhomoserine
name: Acetylhomoserine + Hydrogen sulfide → Acetic acid + Homocysteine + Hydrogen Ion
conversion direction: LEFT_TO_RIGHT

Reference/CAS 7783-06-4
type: UnificationXref
id: 7783-06-4
db: CAS

4.4.1.8
type: BiochemicalReaction
participant stoichiometry: Compound/PW C022608/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000067/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000590/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000164/Stoichiometry/1.0
right: Water
right: L-Cystathionine
spontaneous: false
EC number: 4.4.1.8
left: Homocysteine
left: Ammonium
left: Pyruvic acid
name: Ammonium + Homocysteine + Pyruvic acid → L-Cystathionine + Water
conversion direction: LEFT_TO_RIGHT

cystathionine beta-synthase
type: ProteinReference
xref: Reference/UniProt P32582

cystathionine beta-lyase subunit 2
type: ProteinReference
xref: Reference/UniProt P53101

4.2.1.22
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000067/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000590/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000120/Stoichiometry/1.0
right: Water
right: L-Cystathionine
spontaneous: false
EC number: 4.2.1.22
left: Homocysteine
left: L-Serine
name: Homocysteine + L-Serine → L-Cystathionine + Water
conversion direction: LEFT_TO_RIGHT

Reference/HMDB HMDB0029423
type: UnificationXref
id: HMDB0029423
db: HMDB

homoserine O-trans-acetylase
type: ProteinReference
xref: Reference/UniProt P08465

Compound/PW C000120/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Serine
stoichiometric coefficient: 1.0

cystathionine gamma-lyase
type: ProteinReference
xref: Reference/UniProt P31373

Reference/CAS 53-57-6
type: UnificationXref
id: 53-57-6
db: CAS

Compound/PW C000123/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Aspartic acid
stoichiometric coefficient: 1.0

aspartic beta semi-aldehyde dehydrogenase
type: ProteinReference
xref: Reference/UniProt P13663

Homoserine dehydrogenase
type: ProteinReference
xref: Reference/UniProt P31116

Reference/PubChem-compound 44367445
type: UnificationXref
id: 44367445
db: PubChem-compound

Cysteine Metabolism
type: Pathway
pathway order: PathwayEnzymeReaction/24910
pathway order: PathwayEnzymeReaction/24921
pathway order: PathwayEnzymeReaction/24911
pathway order: PathwayEnzymeReaction/24912
pathway order: PathwayEnzymeReaction/24913
pathway order: PathwaySubPathway/111231
pathway order: PathwayEnzymeReaction/24914
pathway order: PathwayEnzymeReaction/24915
pathway order: PathwayEnzymeReaction/24916
pathway order: PathwayEnzymeReaction/24917
pathway order: PathwayEnzymeReaction/24920
pathway order: PathwayEnzymeReaction/24918
pathway order: PathwayEnzymeReaction/24919
pathway component: ReactionCatalysis6231
pathway component: ReactionCatalysis6230
pathway component: Reaction2903
pathway component: 2.7.2.4
pathway component: Reaction6305
pathway component: ReactionCatalysis6229
pathway component: 2.3.1.31
pathway component: 2.5.1.49,2.5.1.47
pathway component: 4.4.1.8
pathway component: ReactionCatalysis6233
pathway component: 4.2.1.22
pathway component: ReactionCatalysis6232
pathway component: ReactionCatalysis6228
pathway component: 4.4.1.1
pathway component: Reaction6146
pathway component: ReactionCatalysis6227
pathway component: Reaction6301
pathway component: ReactionCatalysis6226
pathway component: 1.1.1.3
pathway component: Endocytosis
pathway component: ReactionCatalysis6225
pathway component: 1.2.1.11
xref: Reference/SMPDB SMP0002309
xref: Reference/PathWhiz PW002383
organism: Saccharomyces cerevisiae

Reference/ChEBI CHEBI 17482
type: UnificationXref
id: CHEBI:17482
db: ChEBI

Reference/PathWhiz PW002383
type: UnificationXref
id: PW002383
db: PathWhiz

Compound/PW C000590/Stoichiometry/1.0
type: Stoichiometry
physical entity: Homocysteine
stoichiometric coefficient: 1.0

Reference/KEGG Compound C01342
type: UnificationXref
id: C01342
db: KEGG Compound

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

Reference/ChEBI CHEBI 28938
type: UnificationXref
id: CHEBI:28938
db: ChEBI

Reference/PubChem-compound 5951
type: UnificationXref
id: 5951
db: PubChem-compound

Compound/PW C000570/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Homoserine
stoichiometric coefficient: 1.0

Reference/BioCyc NAD(P)
type: UnificationXref
id: NAD(P)
db: BioCyc

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

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

ChemicalStructure/PW C000590
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CCS)C(O)=O

aspartokinase
type: ProteinReference
xref: Reference/UniProt P10869

Reference/ChemSpider 12126
type: UnificationXref
id: 12126
db: ChemSpider

Hydrogen sulfide
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 16136
xref: Reference/BioCyc HS
xref: Reference/KEGG Compound C00283
xref: Reference/PubChem-compound 18779926
xref: Reference/CAS 7783-06-4
xref: Reference/ChemSpider 391
xref: Reference/HMDB HMDB0003276
chemical formula: H2S
molecular weight: 33.98772
structure: ChemicalStructure/PW C001827

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 C000003/Stoichiometry/1.0
type: Stoichiometry
physical entity: 2-Ketobutyric acid
stoichiometric coefficient: 1.0

Reference/KEGG Compound C00022
type: UnificationXref
id: C00022
db: KEGG Compound

Reference/KEGG Compound C00263
type: UnificationXref
id: C00263
db: KEGG Compound

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

Reference/CAS 56-88-2
type: UnificationXref
id: 56-88-2
db: CAS

Reference/ChemSpider 5653
type: UnificationXref
id: 5653
db: ChemSpider

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

Compound/PW C007794/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Aspartate-semialdehyde
stoichiometric coefficient: 1.0

Reference/HMDB HMDB0000243
type: UnificationXref
id: HMDB0000243
db: HMDB

ChemicalStructure/PW C000120
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CO)C(O)=O

Adenosine diphosphate
type: SmallMolecule
entity reference: Adenosine diphosphate

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

Adenosine diphosphate
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00008
xref: Reference/PubChem-compound 6022
xref: Reference/ChemSpider 5800
xref: Reference/CAS 58-64-0
xref: Reference/BioCyc ADP
xref: Reference/ChEBI CHEBI 16761
xref: Reference/HMDB HMDB0001341
chemical formula: C10H15N5O10P2
molecular weight: 427.02942
structure: ChemicalStructure/PW C001034

L-Cystathionine
type: SmallMolecule
entity reference: L-Cystathionine

Reference/HMDB HMDB0000005
type: UnificationXref
id: HMDB0000005
db: HMDB

ChemicalStructure/PW C000003
type: ChemicalStructure
structure format: SMILES
structure data: CCC(=O)C(O)=O

ChemicalStructure/PW C000123
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CC(O)=O)C(O)=O

ChemicalStructure/PW C007794
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CC=O)C(O)=O

ChemicalStructure/PW C007795
type: ChemicalStructure
structure format: SMILES
structure data: NC(CC(=O)OP(O)(O)=O)C(O)=O

L-Cystathionine
type: SmallMoleculeReference
xref: Reference/KEGG Compound C02291
xref: Reference/BioCyc L-CYSTATHIONINE
xref: Reference/PubChem-compound 25243997
xref: Reference/ChEBI CHEBI 17482
xref: Reference/ChemSpider 388392
xref: Reference/CAS 56-88-2
xref: Reference/HMDB HMDB0000099
chemical formula: C7H14N2O4S
molecular weight: 222.06743
structure: ChemicalStructure/PW C000067

Compound/PW C000143/Stoichiometry/1.0
type: Stoichiometry
physical entity: NADP
stoichiometric coefficient: 1.0

Reference/SMPDB SMP0002309
type: UnificationXref
id: SMP0002309
db: SMPDB

Reference/KEGG Compound C00033
type: UnificationXref
id: C00033
db: KEGG Compound

Reference/CAS 52-90-4
type: UnificationXref
id: 52-90-4
db: CAS

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

L-Homoserine
type: SmallMolecule
entity reference: L-Homoserine

Reference/ChEBI CHEBI 30831
type: UnificationXref
id: CHEBI:30831
db: ChEBI

2.7.2.4
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000123/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000414/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C007795/Stoichiometry/1.0
right: Adenosine diphosphate
right: L-Aspartyl-4-phosphate
spontaneous: false
EC number: 2.7.2.4
left: L-Aspartic acid
left: Adenosine triphosphate
name: Adenosine triphosphate + L-Aspartic acid → Adenosine diphosphate + L-Aspartyl-4-phosphate
conversion direction: LEFT_TO_RIGHT

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

Reaction6305
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040921/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000448/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001827/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Hydrogen sulfide
right: Hydrogen Ion
right: 2-aminoprop-2-enoate
spontaneous: false
left: L-Cysteine
name: L-Cysteine → 2-aminoprop-2-enoate + Hydrogen Ion + Hydrogen sulfide
conversion direction: LEFT_TO_RIGHT

Water
type: SmallMolecule
entity reference: Water

Reference/KEGG Compound C00283
type: UnificationXref
id: C00283
db: KEGG Compound

Reference/PubChem-compound 528
type: UnificationXref
id: 528
db: PubChem-compound

Reference/UniProt P32582
type: UnificationXref
id: P32582
db: UniProt

Reference/UniProt P31373
type: UnificationXref
id: P31373
db: UniProt

4.4.1.1
type: BiochemicalReaction
participant stoichiometry: Compound/PW C022608/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000448/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000003/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000067/Stoichiometry/1.0
right: Ammonium
right: 2-Ketobutyric acid
right: L-Cysteine
spontaneous: false
EC number: 4.4.1.1
left: Water
left: L-Cystathionine
name: L-Cystathionine + Water → 2-Ketobutyric acid + Ammonium + L-Cysteine
conversion direction: LEFT_TO_RIGHT

Reaction6301
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000029/Stoichiometry/1.0
participant stoichiometry: Compound/PW C010666/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000448/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000067/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: L-Cystathionine
right: Hydrogen Ion
right: Acetic acid
spontaneous: true
left: Acetylhomoserine
left: L-Cysteine
name: Acetylhomoserine + L-Cysteine → Acetic acid + Hydrogen Ion + L-Cystathionine
conversion direction: LEFT_TO_RIGHT

1.1.1.3
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000146/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000570/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000143/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C007794/Stoichiometry/1.0
right: L-Homoserine
right: NADP
spontaneous: false
EC number: 1.1.1.3
left: L-Aspartate-semialdehyde
left: Hydrogen Ion
left: NADPH
name: Hydrogen Ion + L-Aspartate-semialdehyde + NADPH → L-Homoserine + NADP
conversion direction: LEFT_TO_RIGHT

1.2.1.11
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000146/Stoichiometry/1.0
participant stoichiometry: Compound/PW C007795/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000143/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001104/Stoichiometry/1.0
participant stoichiometry: Compound/PW C007794/Stoichiometry/1.0
right: NADP
right: L-Aspartate-semialdehyde
right: Phosphate
spontaneous: false
EC number: 1.2.1.11
left: Hydrogen Ion
left: L-Aspartyl-4-phosphate
left: NADPH
name: Hydrogen Ion + L-Aspartyl-4-phosphate + NADPH → L-Aspartate-semialdehyde + NADP + Phosphate
conversion direction: LEFT_TO_RIGHT

Reference/HMDB HMDB0001341
type: UnificationXref
id: HMDB0001341
db: HMDB

Reference/ChEBI CHEBI 15699
type: UnificationXref
id: CHEBI:15699
db: ChEBI

Reference/HMDB HMDB0012249
type: UnificationXref
id: HMDB0012249
db: HMDB

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

Reference/ChemSpider 5675
type: UnificationXref
id: 5675
db: ChemSpider

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

ChemicalStructure/PW C001827
type: ChemicalStructure
structure format: SMILES
structure data: S

Reference/KEGG Compound C00049
type: UnificationXref
id: C00049
db: KEGG Compound

L-Cysteine
type: SmallMolecule
entity reference: L-Cysteine

Coenzyme A
type: SmallMolecule
entity reference: Coenzyme A

ChemicalStructure/PW C001034
type: ChemicalStructure
structure format: SMILES

Compound/PW C040921/Stoichiometry/1.0
type: Stoichiometry
physical entity: 2-aminoprop-2-enoate
stoichiometric coefficient: 1.0

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

Reference/CAS 14798-03-9
type: UnificationXref
id: 14798-03-9
db: CAS

ChemicalStructure/PW C000067
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CCSC[C@H](N)C(O)=O)C(O)=O

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

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

ChemicalStructure/PW C000029
type: ChemicalStructure
structure format: SMILES
structure data: CC(O)=O

Reference/PubChem-compound 12647
type: UnificationXref
id: 12647
db: PubChem-compound

ChemicalStructure/PW C000940
type: ChemicalStructure
structure format: SMILES

Reference/HMDB HMDB0012250
type: UnificationXref
id: HMDB0012250
db: HMDB

Compound/PW C000164/Stoichiometry/1.0
type: Stoichiometry
physical entity: Pyruvic acid
stoichiometric coefficient: 1.0

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

Reference/CAS 127-17-3
type: UnificationXref
id: 127-17-3
db: CAS

Reference/BioCyc L-BETA-ASPARTYL-P
type: UnificationXref
id: L-BETA-ASPARTYL-P
db: BioCyc

2-iminopropanoate
type: SmallMolecule
entity reference: 2-iminopropanoate

cystathionine beta-lyase
type: Complex
component: cystathionine beta-lyase
component: cystathionine beta-lyase subunit 2

Compound/PW C000029/Stoichiometry/1.0
type: Stoichiometry
physical entity: Acetic acid
stoichiometric coefficient: 1.0

ChemicalStructure/PW C022608
type: ChemicalStructure
structure format: SMILES
structure data: [NH4+]

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

Reference/ChEBI CHEBI 17053
type: UnificationXref
id: CHEBI:17053
db: ChEBI

Reference/KEGG Compound C00065
type: UnificationXref
id: C00065
db: KEGG Compound

2-aminoprop-2-enoate
type: SmallMolecule
entity reference: 2-aminoprop-2-enoate

Reference/ChEBI CHEBI 16761
type: UnificationXref
id: CHEBI:16761
db: ChEBI

Reference/HMDB HMDB0000719
type: UnificationXref
id: HMDB0000719
db: HMDB

ChemicalStructure/PW C000164
type: ChemicalStructure
structure format: SMILES
structure data: CC(=O)C(O)=O

Compound/PW C001827/Stoichiometry/1.0
type: Stoichiometry
physical entity: Hydrogen sulfide
stoichiometric coefficient: 1.0

Compound/PW C007795/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Aspartyl-4-phosphate
stoichiometric coefficient: 1.0

Reference/HMDB HMDB0000042
type: UnificationXref
id: HMDB0000042
db: HMDB

Endocytosis
type: Pathway
pathway order: SubPathwayInteractionSteps/SubPathway111231
pathway component: SubPathwayInteraction111231
name: SubPathway

Reference/ChEBI CHEBI 15366
type: UnificationXref
id: CHEBI:15366
db: ChEBI

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

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

Reference/ChemSpider 5800
type: UnificationXref
id: 5800
db: ChemSpider

Reference/ChemSpider 388392
type: UnificationXref
id: 388392
db: ChemSpider

Phosphate
type: SmallMolecule
entity reference: Phosphate

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

Reference/PubChem-compound 439235
type: UnificationXref
id: 439235
db: PubChem-compound

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

Reference/ChEBI CHEBI 77456
type: UnificationXref
id: CHEBI:77456
db: ChEBI

Reference/CAS 7540-67-2
type: UnificationXref
id: 7540-67-2
db: CAS

Reference/ChemSpider 171
type: UnificationXref
id: 171
db: ChemSpider

Reference/ChEBI CHEBI 32816
type: UnificationXref
id: CHEBI:32816
db: ChEBI

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

Reference/CAS 15106-57-7
type: UnificationXref
id: 15106-57-7
db: CAS

Homocysteine
type: SmallMoleculeReference
xref: Reference/KEGG Compound C05330
xref: Reference/CAS 454-29-5
xref: Reference/HMDB HMDB0000742
xref: Reference/ChEBI CHEBI 17230
xref: Reference/ChemSpider 757
xref: Reference/PubChem-compound 49791978
xref: Reference/BioCyc HOMO-CYS
chemical formula: C4H9NO2S
molecular weight: 135.0354
structure: ChemicalStructure/PW C000590

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/BioCyc PYRUVATE
type: UnificationXref
id: PYRUVATE
db: BioCyc

Reference/PubChem-compound 832
type: UnificationXref
id: 832
db: PubChem-compound

Reference/CAS 58-64-0
type: UnificationXref
id: 58-64-0
db: CAS

Reference/CAS 56-45-1
type: UnificationXref
id: 56-45-1
db: CAS

ChemicalStructure/PW C000414
type: ChemicalStructure
structure format: SMILES

Reference/PubChem-compound 5886
type: UnificationXref
id: 5886
db: PubChem-compound

2-Ketobutyric acid
type: SmallMolecule
entity reference: 2-Ketobutyric acid

Reference/ChEBI CHEBI 7671
type: UnificationXref
id: CHEBI:7671
db: ChEBI

Reference/BioCyc HOMO-CYS
type: UnificationXref
id: HOMO-CYS
db: BioCyc

Compound/PW C022608/Stoichiometry/1.0
type: Stoichiometry
physical entity: Ammonium
stoichiometric coefficient: 1.0

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

L-Aspartyl-4-phosphate
type: SmallMoleculeReference
xref: Reference/BioCyc L-BETA-ASPARTYL-P
xref: Reference/KEGG Compound C03082
xref: Reference/ChemSpider 809
xref: Reference/PubChem-compound 832
xref: Reference/CAS 22138-53-0
xref: Reference/HMDB HMDB0012250
chemical formula: C4H8NO7P
molecular weight: 213.00385
structure: ChemicalStructure/PW C007795

L-Aspartic acid
type: SmallMolecule
entity reference: L-Aspartic acid

Reference/HMDB HMDB0000742
type: UnificationXref
id: HMDB0000742
db: HMDB

L-Aspartate-semialdehyde
type: SmallMolecule
entity reference: L-Aspartate-semialdehyde

L-Serine
type: SmallMolecule
entity reference: L-Serine

L-Aspartyl-4-phosphate
type: SmallMolecule
entity reference: L-Aspartyl-4-phosphate

2-Ketobutyric acid
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 30831
xref: Reference/HMDB HMDB0000005
xref: Reference/CAS 600-18-0
xref: Reference/ChemSpider 57
xref: Reference/KEGG Compound C00109
xref: Reference/PubChem-compound 58
xref: Reference/BioCyc 2-OXOBUTANOATE
chemical formula: C4H6O3
molecular weight: 102.03169
structure: ChemicalStructure/PW C000003

L-Aspartic acid
type: SmallMoleculeReference
xref: Reference/PubChem-compound 44367445
xref: Reference/ChemSpider 5745
xref: Reference/ChEBI CHEBI 17053
xref: Reference/HMDB HMDB0000191
xref: Reference/CAS 56-84-8
xref: Reference/KEGG Compound C00049
xref: Reference/BioCyc L-ASPARTATE
chemical formula: C4H7NO4
molecular weight: 133.0375
structure: ChemicalStructure/PW C000123

L-Serine
type: SmallMoleculeReference
xref: Reference/ChemSpider 5736
xref: Reference/ChEBI CHEBI 17115
xref: Reference/CAS 56-45-1
xref: Reference/KEGG Compound C00065
xref: Reference/PubChem-compound 5951
xref: Reference/HMDB HMDB0000187
xref: Reference/BioCyc SER
chemical formula: C3H7NO3
molecular weight: 105.042595
structure: ChemicalStructure/PW C000120

L-Aspartate-semialdehyde
type: SmallMoleculeReference
xref: Reference/PubChem-compound 439235
xref: Reference/HMDB HMDB0012249
xref: Reference/ChEBI CHEBI 18051
xref: Reference/KEGG Compound C00441
xref: Reference/ChemSpider 388372
xref: Reference/CAS 15106-57-7
xref: Reference/BioCyc L-ASPARTATE-SEMIALDEHYDE
chemical formula: C4H7NO3
molecular weight: 117.042595
structure: ChemicalStructure/PW C007794

Reference/HMDB HMDB0000187
type: UnificationXref
id: HMDB0000187
db: HMDB

Reference/UniProt P53101
type: UnificationXref
id: P53101
db: UniProt

L-Cysteine
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0000574
xref: Reference/CAS 52-90-4
xref: Reference/KEGG Compound C00097
xref: Reference/BioCyc CYS
xref: Reference/ChemSpider 5653
xref: Reference/PubChem-compound 5862
xref: Reference/ChEBI CHEBI 17561
chemical formula: C3H7NO2S
molecular weight: 121.01975
structure: ChemicalStructure/PW C000448

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

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

Reference/UniProt P31116
type: UnificationXref
id: P31116
db: UniProt

Reference/PubChem-compound 16741146
type: UnificationXref
id: 16741146
db: PubChem-compound

Reference/PubChem-compound 25243997
type: UnificationXref
id: 25243997
db: PubChem-compound

Reference/ChemSpider 388372
type: UnificationXref
id: 388372
db: ChemSpider

Reference/KEGG Compound C00097
type: UnificationXref
id: C00097
db: KEGG Compound

Reference/ChemSpider 757
type: UnificationXref
id: 757
db: ChemSpider

Reference/BioCyc L-ASPARTATE-SEMIALDEHYDE
type: UnificationXref
id: L-ASPARTATE-SEMIALDEHYDE
db: BioCyc

Reference/ChemSpider 513
type: UnificationXref
id: 513
db: ChemSpider

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

Reference/PubChem-compound 22833512
type: UnificationXref
id: 22833512
db: PubChem-compound

Reference/BioCyc HOMO-SER
type: UnificationXref
id: HOMO-SER
db: BioCyc

Homocysteine
type: SmallMolecule
entity reference: Homocysteine

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

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/ChEBI CHEBI 18051
type: UnificationXref
id: CHEBI:18051
db: ChEBI

Reference/HMDB HMDB0000191
type: UnificationXref
id: HMDB0000191
db: HMDB

ChemicalStructure/PW C010666
type: ChemicalStructure
structure format: SMILES
structure data: CC(=O)OCCC(N)C(O)=O

L-Homoserine
type: SmallMoleculeReference
xref: Reference/BioCyc HOMO-SER
xref: Reference/ChEBI CHEBI 15699
xref: Reference/CAS 672-15-1
xref: Reference/KEGG Compound C00263
xref: Reference/PubChem-compound 12647
xref: Reference/HMDB HMDB0000719
xref: Reference/ChemSpider 12126
chemical formula: C4H9NO3
molecular weight: 119.05824
structure: ChemicalStructure/PW C000570

Reference/PubChem-compound 1060
type: UnificationXref
id: 1060
db: PubChem-compound

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

Reference/UniProt P08465
type: UnificationXref
id: P08465
db: UniProt

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

Reference/HMDB HMDB0041827
type: UnificationXref
id: HMDB0041827
db: HMDB

cystathionine gamma-lyase
type: Protein
entity reference: cystathionine gamma-lyase

Homoserine dehydrogenase
type: Protein
entity reference: Homoserine dehydrogenase

Reference/CAS 56-84-8
type: UnificationXref
id: 56-84-8
db: CAS

aspartic beta semi-aldehyde dehydrogenase
type: Protein
entity reference: aspartic beta semi-aldehyde dehydrogenase

aspartokinase
type: Protein
entity reference: aspartokinase

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

Reference/PubChem-compound 176
type: UnificationXref
id: 176
db: PubChem-compound

Reference/KEGG Compound C02291
type: UnificationXref
id: C02291
db: KEGG Compound

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