Reference/ChEBI CHEBI 16015
type: UnificationXref
id: CHEBI:16015
db: ChEBI

Reference/KEGG Compound C00437
type: UnificationXref
id: C00437
db: KEGG Compound

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

Reference/PubChem-compound 6262
type: UnificationXref
id: 6262
db: PubChem-compound

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

Argininosuccinate lyase, chloroplastic
type: Protein
entity reference: Argininosuccinate lyase, chloroplastic

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

Ornithine carbamoyltransferase, chloroplastic
type: Protein
entity reference: Ornithine carbamoyltransferase, chloroplastic

Carbamoyl-phosphate synthase large chain, chloroplastic
type: Protein
entity reference: Carbamoyl-phosphate synthase large chain, chloroplastic

Carbamoyl-phosphate synthase small chain, chloroplastic
type: Protein
entity reference: Carbamoyl-phosphate synthase small chain, chloroplastic

Argininosuccinate synthase, chloroplastic
type: Protein
entity reference: Argininosuccinate synthase, chloroplastic

Arginase 2, mitochondrial
type: Protein
entity reference: Arginase 2, mitochondrial

Arginine biosynthesis bifunctional protein ArgJ, chloroplastic
type: Protein
entity reference: Arginine biosynthesis bifunctional protein ArgJ, chloroplastic

Acetylornithine deacetylase
type: Protein
entity reference: Acetylornithine deacetylase

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

Reference/CAS 110-17-8
type: UnificationXref
id: 110-17-8
db: CAS

Reference/ChemSpider 50
type: UnificationXref
id: 50
db: ChemSpider

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

Reference/HMDB HMDB0003364
type: UnificationXref
id: HMDB0003364
db: HMDB

Reference/ChemSpider 388369
type: UnificationXref
id: 388369
db: ChemSpider

Reference/KEGG Compound C00327
type: UnificationXref
id: C00327
db: KEGG Compound

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

NAD
type: SmallMolecule
entity reference: NAD

Compound/PW C000036/Stoichiometry/1.0
type: Stoichiometry
physical entity: Argininosuccinic acid
stoichiometric coefficient: 1.0

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

Citrulline
type: SmallMolecule
entity reference: Citrulline

Reference/ChEBI CHEBI 17594
type: UnificationXref
id: CHEBI:17594
db: ChEBI

Reference/ChEBI CHEBI 17232
type: UnificationXref
id: CHEBI:17232
db: ChEBI

Acetylglutamate kinase, chloroplastic
type: Protein
entity reference: Acetylglutamate kinase, chloroplastic

Probable N-acetyl-gamma-glutamyl-phosphate reductase, chloroplastic
type: Protein
entity reference: Probable N-acetyl-gamma-glutamyl-phosphate reductase, chloroplastic

Compound/PW C000095/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Glutamic acid
stoichiometric coefficient: 1.0

Alanine--glyoxylate aminotransferase 2 homolog 1, mitochondrial
type: Protein
entity reference: Alanine--glyoxylate aminotransferase 2 homolog 1, mitochondrial

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

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

Reference/UniProt Q9C5C4
type: UnificationXref
id: Q9C5C4
db: UniProt

Reference/ChEBI CHEBI 17203
type: UnificationXref
id: CHEBI:17203
db: ChEBI

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

Reference/ChemSpider 5746
type: UnificationXref
id: 5746
db: ChemSpider

Reference/BioCyc HCO3
type: UnificationXref
id: HCO3
db: BioCyc

Reference/ChemSpider 5745
type: UnificationXref
id: 5745
db: ChemSpider

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

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

Reference/ChemSpider 1143
type: UnificationXref
id: 1143
db: ChemSpider

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

Reference/PubChem-compound 192878
type: UnificationXref
id: 192878
db: PubChem-compound

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

Reference/UniProt Q9SCL7
type: UnificationXref
id: Q9SCL7
db: UniProt

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

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

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

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

Reference/PubChem-compound 16950
type: UnificationXref
id: 16950
db: PubChem-compound

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

ChemicalStructure/PW C001099
type: ChemicalStructure
structure format: SMILES

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

Reference/HMDB HMDB0001096
type: UnificationXref
id: HMDB0001096
db: HMDB

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

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

Hydrogen Ion
type: SmallMolecule
entity reference: Hydrogen Ion

L-Glutamine
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0000641
xref: Reference/ChEBI CHEBI 18050
xref: Reference/ChemSpider 5746
xref: Reference/BioCyc GLN
xref: Reference/KEGG Compound C00064
xref: Reference/PubChem-compound 5961
xref: Reference/CAS 56-85-9
chemical formula: C5H10N2O3
molecular weight: 146.06914
structure: ChemicalStructure/PW C000500

Carbamoyl phosphate
type: SmallMoleculeReference
xref: Reference/PubChem-compound 278
xref: Reference/BioCyc CARBAMOYL-P
xref: Reference/ChemSpider 272
xref: Reference/HMDB HMDB0001096
xref: Reference/CAS 590-55-6
xref: Reference/KEGG Compound C00169
xref: Reference/ChEBI CHEBI 17672
chemical formula: CH4NO5P
molecular weight: 140.98271
structure: ChemicalStructure/PW C000862

Reference/KEGG Compound C00472
type: UnificationXref
id: C00472
db: KEGG Compound

Adenosine triphosphate
type: SmallMolecule
entity reference: Adenosine triphosphate

Reference/PubChem-compound 193305
type: UnificationXref
id: 193305
db: PubChem-compound

Quinone
type: SmallMolecule
entity reference: Quinone

Compound/PW C000463/Stoichiometry/1.0
type: Stoichiometry
physical entity: Hydrogen carbonate
stoichiometric coefficient: 1.0

Reference/UniProt Q9SZX3
type: UnificationXref
id: Q9SZX3
db: UniProt

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

Reference/ChemSpider 1159
type: UnificationXref
id: 1159
db: ChemSpider

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

Protein/11074/Stoichiometry/2.0
type: Stoichiometry
physical entity: Acetylornithine deacetylase
stoichiometric coefficient: 2.0

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

Compound/PW C000500/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Glutamine
stoichiometric coefficient: 1.0

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

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

Reference/KEGG Compound C00122
type: UnificationXref
id: C00122
db: KEGG Compound

N-Acetylornithine
type: SmallMolecule
entity reference: N-Acetylornithine

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

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

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

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

N-Acetyl-L-glutamic acid
type: SmallMolecule
entity reference: N-Acetyl-L-glutamic acid

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

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

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

Reference/UniProt P92983
type: UnificationXref
id: P92983
db: UniProt

Reference/CAS 6205-08-9
type: UnificationXref
id: 6205-08-9
db: CAS

Reference/CAS 496-92-4
type: UnificationXref
id: 496-92-4
db: CAS

Compound/PW C001034/Stoichiometry/2.0
type: Stoichiometry
physical entity: Adenosine diphosphate
stoichiometric coefficient: 2.0

Compound/PW C000106/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Proline
stoichiometric coefficient: 1.0

Citrulline
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00327
xref: Reference/CAS 372-75-8
xref: Reference/ChEBI CHEBI 16349
xref: Reference/PubChem-compound 6992098
xref: Reference/BioCyc L-CITRULLINE
xref: Reference/HMDB HMDB0000904
xref: Reference/ChemSpider 9367
chemical formula: C6H13N3O3
molecular weight: 175.09569
structure: ChemicalStructure/PW C000723

Reference/CAS 372-75-8
type: UnificationXref
id: 372-75-8
db: CAS

Reference/KEGG Compound C03406
type: UnificationXref
id: C03406
db: KEGG 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

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

Reference/UniProt Q93Z70
type: UnificationXref
id: Q93Z70
db: UniProt

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

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

Reference/HMDB HMDB0000904
type: UnificationXref
id: HMDB0000904
db: HMDB

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

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

Unknown
type: ProteinReference

Reference/HMDB HMDB0006456
type: UnificationXref
id: HMDB0006456
db: HMDB

Compound/PW C001856/Stoichiometry/1.0
type: Stoichiometry
physical entity: N-Acetylornithine
stoichiometric coefficient: 1.0

Reference/UniProt O50039
type: UnificationXref
id: O50039
db: UniProt

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

Protein/11061/Stoichiometry/2.0
type: Stoichiometry
physical entity: Acetylglutamate kinase, chloroplastic
stoichiometric coefficient: 2.0

Compound/PW C002771/Stoichiometry/1.0
type: Stoichiometry
physical entity: N-Acetyl-L-glutamate 5-semialdehyde
stoichiometric coefficient: 1.0

Protein/11067/Stoichiometry/4.0
type: Stoichiometry
physical entity: Argininosuccinate synthase, chloroplastic
stoichiometric coefficient: 4.0

L-Glutamine
type: SmallMolecule
entity reference: L-Glutamine

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

Carbamoyl phosphate
type: SmallMolecule
entity reference: Carbamoyl phosphate

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

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

Reference/KEGG Compound C00148
type: UnificationXref
id: C00148
db: KEGG Compound

Reference/KEGG Compound C00026
type: UnificationXref
id: C00026
db: KEGG Compound

Reference/KEGG Compound C00025
type: UnificationXref
id: C00025
db: KEGG Compound

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

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

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

Reference/PubChem-compound 769
type: UnificationXref
id: 769
db: PubChem-compound

Hydroquinone
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0002434
xref: Reference/ChemSpider 764
xref: Reference/PubChem-compound 785
xref: Reference/CAS 123-31-9
xref: Reference/BioCyc 236-TRICHLOROHYDROQUINONE
xref: Reference/ChEBI CHEBI 17594
xref: Reference/KEGG Compound C00530
chemical formula: C6H6O2
molecular weight: 110.03678
structure: ChemicalStructure/PW C001632

Compound/PW C000888/Stoichiometry/1.0
type: Stoichiometry
physical entity: N-Acetyl-L-glutamic acid
stoichiometric coefficient: 1.0

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

Reference/UniProt Q6NKX1
type: UnificationXref
id: Q6NKX1
db: UniProt

Reference/ChemSpider 9367
type: UnificationXref
id: 9367
db: ChemSpider

Compound/PW C000862/Stoichiometry/1.0
type: Stoichiometry
physical entity: Carbamoyl phosphate
stoichiometric coefficient: 1.0

Reference/CAS 328-50-7
type: UnificationXref
id: 328-50-7
db: CAS

Reference/HMDB HMDB0000134
type: UnificationXref
id: HMDB0000134
db: HMDB

ChemicalStructure/PW C001144
type: ChemicalStructure
structure format: SMILES

Reference/HMDB HMDB0002434
type: UnificationXref
id: HMDB0002434
db: HMDB

Water
type: SmallMolecule
entity reference: Water

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

Reference/KEGG Compound C01250
type: UnificationXref
id: C01250
db: KEGG Compound

Compound/PW C000200/Stoichiometry/1.0
type: Stoichiometry
physical entity: Urea
stoichiometric coefficient: 1.0

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

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

L-Glutamic γ-semialdehyde
type: SmallMolecule
entity reference: L-Glutamic γ-semialdehyde

Reference/ChemSpider 128566
type: UnificationXref
id: 128566
db: ChemSpider

N-Acetyl-L-glutamyl 5-phosphate
type: SmallMolecule
entity reference: N-Acetyl-L-glutamyl 5-phosphate

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

Reference/KEGG Compound C00169
type: UnificationXref
id: C00169
db: KEGG Compound

Reference/KEGG Compound C00288
type: UnificationXref
id: C00288
db: KEGG Compound

Reference/CAS 56-85-9
type: UnificationXref
id: 56-85-9
db: CAS

ChemicalStructure/PW C001034
type: ChemicalStructure
structure format: SMILES

Reference/ChemSpider 764
type: UnificationXref
id: 764
db: ChemSpider

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

Urea
type: SmallMolecule
entity reference: Urea

Reference/HMDB HMDB0000148
type: UnificationXref
id: HMDB0000148
db: HMDB

Urea
type: SmallMoleculeReference
xref: Reference/BioCyc UREA
xref: Reference/CAS 57-13-6
xref: Reference/KEGG Compound C00086
xref: Reference/HMDB HMDB0000294
xref: Reference/ChemSpider 1143
xref: Reference/PubChem-compound 1176
xref: Reference/ChEBI CHEBI 16199
chemical formula: CH4N2O
molecular weight: 60.032364
structure: ChemicalStructure/PW C000200

Compound/PW C001632/Stoichiometry/1.0
type: Stoichiometry
physical entity: Hydroquinone
stoichiometric coefficient: 1.0

Reference/ChemSpider 10197150
type: UnificationXref
id: 10197150
db: ChemSpider

N-Acetyl-L-glutamic acid
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00624
xref: Reference/ChEBI CHEBI 12575
xref: Reference/HMDB HMDB0001138
xref: Reference/BioCyc ACETYL-GLU
xref: Reference/CAS 1188-37-0
xref: Reference/PubChem-compound 185
xref: Reference/ChemSpider 180
chemical formula: C7H11NO5
molecular weight: 189.06372
structure: ChemicalStructure/PW C000888

Reference/PubChem-compound 785
type: UnificationXref
id: 785
db: PubChem-compound

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

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

N-Acetylornithine
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 16543
xref: Reference/ChemSpider 388369
xref: Reference/KEGG Compound C00437
xref: Reference/CAS 6205-08-9
xref: Reference/HMDB HMDB0003357
xref: Reference/PubChem-compound 439232
xref: Reference/BioCyc N-ALPHA-ACETYLORNITHINE
chemical formula: C7H14N2O3
molecular weight: 174.10045
structure: ChemicalStructure/PW C001856

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

Reference/ChEBI CHEBI 18012
type: UnificationXref
id: CHEBI:18012
db: ChEBI

Reference/ChEBI CHEBI 16199
type: UnificationXref
id: CHEBI:16199
db: ChEBI

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

ChemicalStructure/PW C000396
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CCCNC(N)=N)C(O)=O

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

ChemicalStructure/PW C000032
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C000036
type: ChemicalStructure
structure format: SMILES

Reference/KEGG Compound C00062
type: UnificationXref
id: C00062
db: KEGG Compound

Quinone
type: SmallMoleculeReference
xref: Reference/ChemSpider 4489
xref: Reference/CAS 106-51-4
xref: Reference/KEGG Compound C00472
xref: Reference/ChEBI CHEBI 16509
xref: Reference/BioCyc CPD-8130
xref: Reference/PubChem-compound 4650
xref: Reference/HMDB HMDB0003364
chemical formula: C6H4O2
molecular weight: 108.021126
structure: ChemicalStructure/PW C001860

ChemicalStructure/PW C001003
type: ChemicalStructure
structure format: SMILES
structure data: OC(=O)C1CCC=N1

Reference/CAS 56-86-0
type: UnificationXref
id: 56-86-0
db: CAS

Reference/CAS 590-55-6
type: UnificationXref
id: 590-55-6
db: CAS

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

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

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

Compound/PW C002749/Stoichiometry/1.0
type: Stoichiometry
physical entity: N-Acetyl-L-glutamyl 5-phosphate
stoichiometric coefficient: 1.0

Reference/KEGG Compound C00064
type: UnificationXref
id: C00064
db: KEGG Compound

Hydroquinone
type: SmallMolecule
entity reference: Hydroquinone

Reference/CAS 2387-71-5
type: UnificationXref
id: 2387-71-5
db: CAS

Reference/HMDB HMDB0002104
type: UnificationXref
id: HMDB0002104
db: HMDB

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

Reference/HMDB HMDB0001138
type: UnificationXref
id: HMDB0001138
db: HMDB

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

Reference/HMDB HMDB0000162
type: UnificationXref
id: HMDB0000162
db: HMDB

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

L-Proline
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 17203
xref: Reference/ChemSpider 128566
xref: Reference/BioCyc PRO
xref: Reference/CAS 147-85-3
xref: Reference/KEGG Compound C00148
xref: Reference/HMDB HMDB0000162
xref: Reference/PubChem-compound 145742
chemical formula: C5H9NO2
molecular weight: 115.06333
structure: ChemicalStructure/PW C000106

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

Compound/PW C001003/Stoichiometry/1.0
type: Stoichiometry
physical entity: 1-Pyrroline-5-carboxylic acid
stoichiometric coefficient: 1.0

Reference/KEGG Compound C00077
type: UnificationXref
id: C00077
db: KEGG Compound

Reference/KEGG Compound C01165
type: UnificationXref
id: C01165
db: KEGG Compound

Phosphate
type: SmallMolecule
entity reference: Phosphate

Reference/PubChem-compound 145742
type: UnificationXref
id: 145742
db: PubChem-compound

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

N-Acetyl-L-glutamate 5-semialdehyde
type: SmallMoleculeReference
xref: Reference/PubChem-compound 192878
xref: Reference/ChemSpider 167387
xref: Reference/CAS 13074-21-0
xref: Reference/KEGG Compound C01250
xref: Reference/HMDB HMDB0006488
xref: Reference/ChEBI CHEBI 16319
chemical formula: C7H11NO4
molecular weight: 173.0688
structure: ChemicalStructure/PW C002771

ReactionCatalysis7109
type: Catalysis
controller: acetylornithine aminotransferase / N-succinyldiaminopimelate aminotransferase
controlled: 2.6.1.11
control type: ACTIVATION

Protein/11063/Stoichiometry/2.0
type: Stoichiometry
physical entity: Alanine--glyoxylate aminotransferase 2 homolog 1, mitochondrial
stoichiometric coefficient: 2.0

Oxoglutaric acid
type: SmallMolecule
entity reference: Oxoglutaric acid

Reference/CAS 15383-57-0
type: UnificationXref
id: 15383-57-0
db: CAS

ReactionCatalysis7108
type: Catalysis
controller: Probable N-acetyl-gamma-glutamyl-phosphate reductase, chloroplastic
controlled: 1.2.1.38
control type: ACTIVATION

ChemicalStructure/PW C000095
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CCC(O)=O)C(O)=O

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

ReactionCatalysis7107
type: Catalysis
controller: acetylglutamate kinase
controlled: 2.7.2.8
control type: ACTIVATION

Reference/HMDB HMDB0000052
type: UnificationXref
id: HMDB0000052
db: HMDB

Reference/HMDB HMDB0000294
type: UnificationXref
id: HMDB0000294
db: HMDB

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

ReactionCatalysis7111
type: Catalysis
controller: argininosuccinate synthase
controlled: Reaction7132
control type: ACTIVATION

ReactionCatalysis7110
type: Catalysis
controller: carbamoyl phosphate synthetase
controlled: 6.3.5.5
control type: ACTIVATION

Reference/UniProt Q9ZUR7
type: UnificationXref
id: Q9ZUR7
db: UniProt

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

Reference/UniProt Q8VZC3
type: UnificationXref
id: Q8VZC3
db: UniProt

Reference/KEGG Compound C00086
type: UnificationXref
id: C00086
db: KEGG Compound

Reference/KEGG Compound C04322
type: UnificationXref
id: C04322
db: KEGG Compound

Reference/UniProt P54904
type: UnificationXref
id: P54904
db: UniProt

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

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

ReactionCatalysis7112
type: Catalysis
controller: Argininosuccinate lyase, chloroplastic
controlled: 4.3.2.1
control type: ACTIVATION

Reference/BioCyc L-GLUTAMATE GAMMA-SEMIALDEHYDE
type: UnificationXref
id: L-GLUTAMATE_GAMMA-SEMIALDEHYDE
db: BioCyc

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

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

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

L-Glutamic γ-semialdehyde
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0002104
xref: Reference/PubChem-compound 193305
xref: Reference/CAS 496-92-4
xref: Reference/ChemSpider 167744
xref: Reference/KEGG Compound C01165
xref: Reference/BioCyc L-GLUTAMATE GAMMA-SEMIALDEHYDE
xref: Reference/ChEBI CHEBI 17232
chemical formula: C5H9NO3
molecular weight: 131.05824
structure: ChemicalStructure/PW C001415

N-Acetyl-L-glutamyl 5-phosphate
type: SmallMoleculeReference
xref: Reference/KEGG Compound C04133
xref: Reference/BioCyc N-ACETYL-GLUTAMYL-P
xref: Reference/ChEBI CHEBI 16878
xref: Reference/CAS 15383-57-0
xref: Reference/ChemSpider 389220
xref: Reference/HMDB HMDB0006456
xref: Reference/PubChem-compound 440236
chemical formula: C7H12NO8P
molecular weight: 269.03006
structure: ChemicalStructure/PW C002749

N-Acetyl-L-glutamate 5-semialdehyde
type: SmallMolecule
entity reference: N-Acetyl-L-glutamate 5-semialdehyde

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

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

Reference/ChEBI CHEBI 18050
type: UnificationXref
id: CHEBI:18050
db: ChEBI

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 HMDB0000191
type: UnificationXref
id: HMDB0000191
db: HMDB

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

ReactionCatalysis7129
type: Catalysis
controller: Arginine biosynthesis bifunctional protein ArgJ, chloroplastic
controlled: 2.3.1.35,2.3.1.1
control type: ACTIVATION

ReactionCatalysis7127
type: Catalysis
controller: acetylornithine deacetylase
controlled: Reaction7148
control type: ACTIVATION

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

ReactionCatalysis7133
type: Catalysis
controller: Arginase, mitochondrial
controlled: 3.5.3.1
control type: ACTIVATION

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

ReactionCatalysis7132
type: Catalysis
controller: Acetylornithine aminotransferase, chloroplastic/mitochondrial
controlled: 2.6.1.11
control type: ACTIVATION

ReactionCatalysis7131
type: Catalysis
controller: Arginine biosynthesis bifunctional protein ArgJ, chloroplastic
controlled: Reaction7152
control type: ACTIVATION

ReactionCatalysis7130
type: Catalysis
controller: Ornithine carbamoyltransferase, chloroplastic
controlled: 2.1.3.3
control type: ACTIVATION

Proline dehydrogenase 1, mitochondrial
type: Protein
entity reference: Proline dehydrogenase 1, mitochondrial

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

Reference/ChemSpider 749
type: UnificationXref
id: 749
db: ChemSpider

Reference/CAS 71-52-3
type: UnificationXref
id: 71-52-3
db: CAS

Reference/UniProt Q9ZPF5
type: UnificationXref
id: Q9ZPF5
db: UniProt

Acetylornithine aminotransferase, chloroplastic/mitochondrial
type: Protein
entity reference: Acetylornithine aminotransferase, chloroplastic/mitochondrial

Arginase 1, mitochondrial
type: Protein
entity reference: Arginase 1, mitochondrial

Delta-1-pyrroline-5-carboxylate dehydrogenase 12A1, mitochondrial
type: Protein
entity reference: Delta-1-pyrroline-5-carboxylate dehydrogenase 12A1, mitochondrial

Pyrroline-5-carboxylate reductase
type: Protein
entity reference: Pyrroline-5-carboxylate reductase

L-Proline
type: SmallMolecule
entity reference: L-Proline

ChemicalStructure/PW C000088
type: ChemicalStructure
structure format: SMILES
structure data: OC(=O)\C=C\C(O)=O

Reference/HMDB HMDB0003357
type: UnificationXref
id: HMDB0003357
db: HMDB

Hydrogen carbonate
type: SmallMolecule
entity reference: Hydrogen carbonate

Proline dehydrogenase 2, mitochondrial
type: Protein
entity reference: Proline dehydrogenase 2, mitochondrial

ReactionCatalysis7137
type: Catalysis
controller: proline dehydrogenase
controlled: 1.5.5.2
control type: ACTIVATION

Compound/PW C000088/Stoichiometry/1.0
type: Stoichiometry
physical entity: Fumaric acid
stoichiometric coefficient: 1.0

ReactionCatalysis7136
type: Catalysis
controller: Unknown
controlled: 2.6.1.13
control type: ACTIVATION

Hydrogen carbonate
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0000595
xref: Reference/ChEBI CHEBI 17544
xref: Reference/PubChem-compound 769
xref: Reference/BioCyc HCO3
xref: Reference/ChemSpider 749
xref: Reference/CAS 71-52-3
xref: Reference/KEGG Compound C00288
chemical formula: CH2O3
molecular weight: 62.000393
structure: ChemicalStructure/PW C000463

ReactionCatalysis7135
type: Catalysis
controller: Pyrroline-5-carboxylate reductase
controlled: 1.5.1.2
control type: ACTIVATION

ReactionCatalysis7134
type: Catalysis
controller: Delta-1-pyrroline-5-carboxylate dehydrogenase 12A1, mitochondrial
controlled: 1.2.1.88
control type: ACTIVATION

Reference/ChemSpider 30572
type: UnificationXref
id: 30572
db: ChemSpider

Compound/PW C001415/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Glutamic γ-semialdehyde
stoichiometric coefficient: 1.0

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

Reference/ChEBI CHEBI 12575
type: UnificationXref
id: CHEBI:12575
db: ChEBI

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

Reference/TAXONOMY 3702
type: UnificationXref
id: 3702
db: TAXONOMY

ChemicalStructure/PW C002749
type: ChemicalStructure
structure format: SMILES
structure data: CC(=O)N[C@@H](CCC(=O)OP(O)(O)=O)C(O)=O

ChemicalStructure/PW C001415
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CCC=O)C(O)=O

NADH
type: SmallMolecule
entity reference: NADH

proline dehydrogenase
type: Complex
component: Proline dehydrogenase 2, mitochondrial
component: Proline dehydrogenase 1, mitochondrial

Reference/CAS 13074-21-0
type: UnificationXref
id: 13074-21-0
db: CAS

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

Reference/PubChem-compound 21883788
type: UnificationXref
id: 21883788
db: PubChem-compound

Arginase, mitochondrial
type: Complex
component: Arginase 2, mitochondrial
component: Arginase 1, mitochondrial

1-Pyrroline-5-carboxylic acid
type: SmallMoleculeReference
xref: Reference/ChemSpider 1159
xref: Reference/HMDB HMDB0001301
xref: Reference/ChEBI CHEBI 1372
xref: Reference/CAS 2906-39-0
xref: Reference/BioCyc l-delta(1)-pyrroline 5-carboxylate
xref: Reference/KEGG Compound C04322
xref: Reference/PubChem-compound 1196
chemical formula: C5H7NO2
molecular weight: 113.047676
structure: ChemicalStructure/PW C001003

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

Argininosuccinic acid
type: SmallMoleculeReference
xref: Reference/KEGG Compound C03406
xref: Reference/ChemSpider 16059
xref: Reference/HMDB HMDB0000052
xref: Reference/PubChem-compound 16950
xref: Reference/CAS 2387-71-5
xref: Reference/ChEBI CHEBI 15682
chemical formula: C10H18N4O6
molecular weight: 290.12262
structure: ChemicalStructure/PW C000036

Reference/CAS 57-13-6
type: UnificationXref
id: 57-13-6
db: CAS

L-Arginine
type: SmallMoleculeReference
xref: Reference/BioCyc ARG
xref: Reference/ChEBI CHEBI 16467
xref: Reference/CAS 74-79-3
xref: Reference/KEGG Compound C00062
xref: Reference/ChemSpider 6082
xref: Reference/PubChem-compound 28782
xref: Reference/HMDB HMDB0000517
chemical formula: C6H14N4O2
molecular weight: 174.11168
structure: ChemicalStructure/PW C000396

Pyrophosphate
type: SmallMolecule
entity reference: Pyrophosphate

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/PubChem-compound 6992098
type: UnificationXref
id: 6992098
db: PubChem-compound

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

Reference/PubChem-compound 5961
type: UnificationXref
id: 5961
db: PubChem-compound

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

Reference/KEGG Compound C04133
type: UnificationXref
id: C04133
db: KEGG Compound

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

Unknown
type: Protein
entity reference: Unknown

Reference/PubChem-compound 51
type: UnificationXref
id: 51
db: PubChem-compound

ChemicalStructure/PW C000463
type: ChemicalStructure
structure format: SMILES
structure data: OC(O)=O

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

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

Reference/ChEBI CHEBI 15729
type: UnificationXref
id: CHEBI:15729
db: ChEBI

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

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

Reference/ChemSpider 167744
type: UnificationXref
id: 167744
db: ChemSpider

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

Argininosuccinic acid
type: SmallMolecule
entity reference: Argininosuccinic acid

1-Pyrroline-5-carboxylic acid
type: SmallMolecule
entity reference: 1-Pyrroline-5-carboxylic acid

L-Arginine
type: SmallMolecule
entity reference: L-Arginine

Adenosine monophosphate
type: SmallMolecule
entity reference: Adenosine monophosphate

4.3.2.1
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000396/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000088/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000036/Stoichiometry/1.0
right: Fumaric acid
right: L-Arginine
spontaneous: false
EC number: 4.3.2.1
left: Argininosuccinic acid
name: Argininosuccinic acid → Fumaric acid + L-Arginine
conversion direction: LEFT_TO_RIGHT

Oxoglutaric acid
type: SmallMoleculeReference
xref: Reference/CAS 328-50-7
xref: Reference/PubChem-compound 51
xref: Reference/BioCyc 2-KETOGLUTARATE
xref: Reference/HMDB HMDB0000208
xref: Reference/ChEBI CHEBI 30915
xref: Reference/KEGG Compound C00026
xref: Reference/ChemSpider 50
chemical formula: C5H6O5
molecular weight: 146.02153
structure: ChemicalStructure/PW C000134

Reference/ChemSpider 272
type: UnificationXref
id: 272
db: ChemSpider

Reaction7132
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000723/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000123/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000032/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000414/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000170/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000036/Stoichiometry/1.0
right: Adenosine monophosphate
right: Argininosuccinic acid
right: Pyrophosphate
spontaneous: false
left: L-Aspartic acid
left: Citrulline
left: Adenosine triphosphate
name: Adenosine triphosphate + Citrulline + L-Aspartic acid → Adenosine monophosphate + Argininosuccinic acid + Pyrophosphate
conversion direction: LEFT_TO_RIGHT

Reference/UniProt Q9LEU8
type: UnificationXref
id: Q9LEU8
db: UniProt

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

Reference/CAS 70-26-8
type: UnificationXref
id: 70-26-8
db: CAS

6.3.5.5
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000095/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000463/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000414/Stoichiometry/2.0
participant stoichiometry: Compound/PW C000500/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001034/Stoichiometry/2.0
participant stoichiometry: Compound/PW C001104/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/2.0
participant stoichiometry: Compound/PW C000862/Stoichiometry/1.0
right: Adenosine diphosphate
right: L-Glutamic acid
right: Hydrogen Ion
right: Carbamoyl phosphate
right: Phosphate
spontaneous: false
EC number: 6.3.5.5
left: Water
left: Hydrogen carbonate
left: L-Glutamine
left: Adenosine triphosphate
name: 2 Adenosine triphosphate + Hydrogen carbonate + L-Glutamine + Water → 2 Adenosine diphosphate + Carbamoyl phosphate + 2 Hydrogen Ion + L-Glutamic acid + Phosphate
conversion direction: LEFT_TO_RIGHT

2.6.1.11
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000095/Stoichiometry/1.0
participant stoichiometry: Compound/PW C002771/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000134/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001856/Stoichiometry/1.0
right: Oxoglutaric acid
right: N-Acetylornithine
spontaneous: false
EC number: 2.6.1.11
left: N-Acetyl-L-glutamate 5-semialdehyde
left: L-Glutamic acid
name: L-Glutamic acid + N-Acetyl-L-glutamate 5-semialdehyde → N-Acetylornithine + Oxoglutaric acid
conversion direction: LEFT_TO_RIGHT

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/UniProt Q9LVW7
type: UnificationXref
id: Q9LVW7
db: UniProt

NADPH
type: SmallMolecule
entity reference: NADPH

Reference/ChemSpider 6026
type: UnificationXref
id: 6026
db: ChemSpider

Reference/PubChem-compound 4650
type: UnificationXref
id: 4650
db: PubChem-compound

Acetic acid
type: SmallMolecule
entity reference: Acetic acid

1.2.1.38
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000146/Stoichiometry/1.0
participant stoichiometry: Compound/PW C002771/Stoichiometry/1.0
participant stoichiometry: Compound/PW C002749/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
right: N-Acetyl-L-glutamate 5-semialdehyde
right: NADP
right: Phosphate
spontaneous: false
EC number: 1.2.1.38
left: Hydrogen Ion
left: N-Acetyl-L-glutamyl 5-phosphate
left: NADPH
name: Hydrogen Ion + N-Acetyl-L-glutamyl 5-phosphate + NADPH → N-Acetyl-L-glutamate 5-semialdehyde + NADP + Phosphate
conversion direction: LEFT_TO_RIGHT

Ornithine
type: SmallMolecule
entity reference: Ornithine

Compound/PW C000414/Stoichiometry/2.0
type: Stoichiometry
physical entity: Adenosine triphosphate
stoichiometric coefficient: 2.0

NADP
type: SmallMolecule
entity reference: NADP

ChemicalStructure/PW C000200
type: ChemicalStructure
structure format: SMILES
structure data: NC(N)=O

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

2.7.2.8
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000414/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000888/Stoichiometry/1.0
participant stoichiometry: Compound/PW C002749/Stoichiometry/1.0
right: Adenosine diphosphate
right: N-Acetyl-L-glutamyl 5-phosphate
spontaneous: false
EC number: 2.7.2.8
left: N-Acetyl-L-glutamic acid
left: Adenosine triphosphate
name: Adenosine triphosphate + N-Acetyl-L-glutamic acid → Adenosine diphosphate + N-Acetyl-L-glutamyl 5-phosphate
conversion direction: LEFT_TO_RIGHT

Ornithine
type: SmallMoleculeReference
xref: Reference/CAS 70-26-8
xref: Reference/HMDB HMDB0000214
xref: Reference/PubChem-compound 6262
xref: Reference/KEGG Compound C00077
xref: Reference/BioCyc L-ORNITHINE
xref: Reference/ChemSpider 6026
xref: Reference/ChEBI CHEBI 15729
chemical formula: C5H12N2O2
molecular weight: 132.08987
structure: ChemicalStructure/PW C000140

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

Reference/HMDB HMDB0000208
type: UnificationXref
id: HMDB0000208
db: HMDB

Reference/BioCyc 236-TRICHLOROHYDROQUINONE
type: UnificationXref
id: 236-TRICHLOROHYDROQUINONE
db: BioCyc

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

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

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

Reference/HMDB HMDB0001301
type: UnificationXref
id: HMDB0001301
db: HMDB

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

Reference/HMDB HMDB0000214
type: UnificationXref
id: HMDB0000214
db: HMDB

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

ChemicalStructure/PW C000134
type: ChemicalStructure
structure format: SMILES
structure data: OC(=O)CCC(=O)C(O)=O

1.2.1.88
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001415/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000095/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000721/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001144/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/2.0
right: NADH
right: L-Glutamic acid
right: Hydrogen Ion
spontaneous: false
EC number: 1.2.1.88
left: Water
left: L-Glutamic γ-semialdehyde
left: NAD
name: L-Glutamic γ-semialdehyde + NAD + Water → 2 Hydrogen Ion + L-Glutamic acid + NADH
conversion direction: LEFT_TO_RIGHT

Reference/ChEBI CHEBI 30915
type: UnificationXref
id: CHEBI:30915
db: ChEBI

3.5.3.1
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000396/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000200/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000140/Stoichiometry/1.0
right: Ornithine
right: Urea
spontaneous: false
EC number: 3.5.3.1
left: Water
left: L-Arginine
name: L-Arginine + Water → Ornithine + Urea
conversion direction: LEFT_TO_RIGHT

2.6.1.13
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000095/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001415/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000140/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000134/Stoichiometry/1.0
right: L-Glutamic acid
right: L-Glutamic γ-semialdehyde
spontaneous: false
EC number: 2.6.1.13
left: Ornithine
left: Oxoglutaric acid
name: Ornithine + Oxoglutaric acid ↔ L-Glutamic acid + L-Glutamic γ-semialdehyde
conversion direction: REVERSIBLE

Reference/BioCyc l-delta(1)-pyrroline 5-carboxylate
type: UnificationXref
id: l-delta(1)-pyrroline_5-carboxylate
db: BioCyc

1.5.1.2
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000146/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001003/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000106/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000143/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/2.0
right: NADP
right: L-Proline
spontaneous: false
EC number: 1.5.1.2
left: 1-Pyrroline-5-carboxylic acid
left: Hydrogen Ion
left: NADPH
name: 1-Pyrroline-5-carboxylic acid + 2 Hydrogen Ion + NADPH → L-Proline + NADP
conversion direction: LEFT_TO_RIGHT

1.5.5.2
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001003/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001632/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000106/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001860/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: 1-Pyrroline-5-carboxylic acid
right: Hydrogen Ion
right: Hydroquinone
spontaneous: false
EC number: 1.5.5.2
left: Quinone
left: L-Proline
name: L-Proline + Quinone → 1-Pyrroline-5-carboxylic acid + Hydrogen Ion + Hydroquinone
conversion direction: LEFT_TO_RIGHT

Argininosuccinate lyase, chloroplastic
type: ProteinReference
xref: Reference/UniProt Q9LEU8

Argininosuccinate synthase, chloroplastic
type: ProteinReference
xref: Reference/UniProt Q9SZX3

Ornithine carbamoyltransferase, chloroplastic
type: ProteinReference
xref: Reference/UniProt O50039

2.1.3.3
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000723/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000140/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001104/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000862/Stoichiometry/1.0
right: Hydrogen Ion
right: Phosphate
right: Citrulline
spontaneous: false
EC number: 2.1.3.3
left: Ornithine
left: Carbamoyl phosphate
name: Carbamoyl phosphate + Ornithine → Citrulline + Hydrogen Ion + Phosphate
conversion direction: LEFT_TO_RIGHT

Alanine--glyoxylate aminotransferase 2 homolog 1, mitochondrial
type: ProteinReference
xref: Reference/UniProt Q940M2

2.3.1.35,2.3.1.1
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000095/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001099/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000940/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000888/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Coenzyme A
right: Hydrogen Ion
right: N-Acetyl-L-glutamic acid
spontaneous: false
EC number: 2.3.1.35,2.3.1.1
left: L-Glutamic acid
left: Acetyl-CoA
name: Acetyl-CoA + L-Glutamic acid → Coenzyme A + Hydrogen Ion + N-Acetyl-L-glutamic acid
conversion direction: LEFT_TO_RIGHT

Carbamoyl-phosphate synthase small chain, chloroplastic
type: ProteinReference
xref: Reference/UniProt Q9LVW7

2.6.1.11
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000095/Stoichiometry/1.0
participant stoichiometry: Compound/PW C002771/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000134/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001856/Stoichiometry/1.0
right: Oxoglutaric acid
right: N-Acetylornithine
spontaneous: false
EC number: 2.6.1.11
left: N-Acetyl-L-glutamate 5-semialdehyde
left: L-Glutamic acid
name: L-Glutamic acid + N-Acetyl-L-glutamate 5-semialdehyde → N-Acetylornithine + Oxoglutaric acid
conversion direction: LEFT_TO_RIGHT

Carbamoyl-phosphate synthase large chain, chloroplastic
type: ProteinReference
xref: Reference/UniProt Q42601

Reaction7152
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000095/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000888/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000140/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001856/Stoichiometry/1.0
right: Ornithine
right: N-Acetyl-L-glutamic acid
spontaneous: false
left: L-Glutamic acid
left: N-Acetylornithine
name: L-Glutamic acid + N-Acetylornithine → N-Acetyl-L-glutamic acid + Ornithine
conversion direction: LEFT_TO_RIGHT

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

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

Probable N-acetyl-gamma-glutamyl-phosphate reductase, chloroplastic
type: ProteinReference
xref: Reference/UniProt Q93Z70

Acetylglutamate kinase, chloroplastic
type: ProteinReference
xref: Reference/UniProt Q9SCL7

ChemicalStructure/PW C000143
type: ChemicalStructure
structure format: SMILES

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

ChemicalStructure/PW C000140
type: ChemicalStructure
structure format: SMILES
structure data: NCCC[C@H](N)C(O)=O

ChemicalStructure/PW C000146
type: ChemicalStructure
structure format: SMILES

Fumaric acid
type: SmallMolecule
entity reference: Fumaric acid

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

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

Fumaric acid
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0000134
xref: Reference/ChemSpider 10197150
xref: Reference/CAS 110-17-8
xref: Reference/PubChem-compound 21883788
xref: Reference/KEGG Compound C00122
xref: Reference/BioCyc FUM
xref: Reference/ChEBI CHEBI 18012
chemical formula: C4H4O4
molecular weight: 116.010956
structure: ChemicalStructure/PW C000088

acetylornithine aminotransferase / N-succinyldiaminopimelate aminotransferase
type: Complex
component stoichiometry: Protein/11063/Stoichiometry/2.0
component: Alanine--glyoxylate aminotransferase 2 homolog 1, mitochondrial

Reaction7148
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000029/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000140/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001856/Stoichiometry/1.0
right: Ornithine
right: Acetic acid
spontaneous: false
left: Water
left: N-Acetylornithine
name: N-Acetylornithine + Water → Acetic acid + Ornithine
conversion direction: LEFT_TO_RIGHT

Proline Metabolism
type: Pathway
pathway order: PathwayEnzymeReaction/26475
pathway order: PathwayEnzymeReaction/26486
pathway order: PathwayEnzymeReaction/26476
pathway order: PathwayEnzymeReaction/26487
pathway order: PathwayEnzymeReaction/26477
pathway order: PathwayEnzymeReaction/26488
pathway order: PathwayEnzymeReaction/26478
pathway order: PathwayEnzymeReaction/26489
pathway order: PathwayEnzymeReaction/26479
pathway order: PathwayEnzymeReaction/26480
pathway order: PathwayEnzymeReaction/26481
pathway order: PathwayEnzymeReaction/26482
pathway order: PathwayEnzymeReaction/26472
pathway order: PathwayEnzymeReaction/26483
pathway order: PathwayEnzymeReaction/26473
pathway order: PathwayEnzymeReaction/26484
pathway order: PathwayEnzymeReaction/26474
pathway order: PathwayEnzymeReaction/26485
pathway component: ReactionCatalysis7109
pathway component: 4.3.2.1
pathway component: 1.2.1.88
pathway component: Reaction7132
pathway component: 3.5.3.1
pathway component: 2.6.1.13
pathway component: 1.5.1.2
pathway component: ReactionCatalysis7108
pathway component: ReactionCatalysis7107
pathway component: ReactionCatalysis7129
pathway component: 1.5.5.2
pathway component: Reaction2721
pathway component: ReactionCatalysis7127
pathway component: ReactionCatalysis7111
pathway component: 2.1.3.3
pathway component: ReactionCatalysis7133
pathway component: Reaction2717
pathway component: ReactionCatalysis7110
pathway component: 2.3.1.35,2.3.1.1
pathway component: ReactionCatalysis7132
pathway component: 6.3.5.5
pathway component: ReactionCatalysis7131
pathway component: 2.6.1.11
pathway component: ReactionCatalysis7130
pathway component: Reaction7152
pathway component: 1.2.1.38
pathway component: ReactionCatalysis7137
pathway component: ReactionCatalysis7136
pathway component: ReactionCatalysis7135
pathway component: ReactionCatalysis7112
pathway component: ReactionCatalysis7134
pathway component: Reaction7148
pathway component: 2.7.2.8
xref: Reference/SMPDB SMP0002420
xref: Reference/PathWhiz PW002526
organism: Arabidopsis thaliana

acetylglutamate kinase
type: Complex
component stoichiometry: Protein/11061/Stoichiometry/2.0
component: Acetylglutamate kinase, chloroplastic

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

Proline dehydrogenase 1, mitochondrial
type: ProteinReference
xref: Reference/UniProt P92983

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

Pyrroline-5-carboxylate reductase
type: ProteinReference
xref: Reference/UniProt P54904

Acetylornithine aminotransferase, chloroplastic/mitochondrial
type: ProteinReference
xref: Reference/UniProt Q9M8M7

Acetylornithine deacetylase
type: ProteinReference
xref: Reference/UniProt Q9C5C4

Delta-1-pyrroline-5-carboxylate dehydrogenase 12A1, mitochondrial
type: ProteinReference
xref: Reference/UniProt Q8VZC3

Arginase 1, mitochondrial
type: ProteinReference
xref: Reference/UniProt P46637

Arginase 2, mitochondrial
type: ProteinReference
xref: Reference/UniProt Q9ZPF5

ChemicalStructure/PW C000106
type: ChemicalStructure
structure format: SMILES
structure data: OC(=O)[C@@H]1CCCN1

Arginine biosynthesis bifunctional protein ArgJ, chloroplastic
type: ProteinReference
xref: Reference/UniProt Q9ZUR7

Reference/HMDB HMDB0000595
type: UnificationXref
id: HMDB0000595
db: HMDB

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

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

Reference/ChemSpider 6082
type: UnificationXref
id: 6082
db: ChemSpider

ChemicalStructure/PW C002771
type: ChemicalStructure
structure format: SMILES
structure data: CC(=O)N[C@@H](CCC=O)C(O)=O

carbamoyl phosphate synthetase
type: Complex
component stoichiometry: Protein/11066/Stoichiometry/2.0
component stoichiometry: Protein/11065/Stoichiometry/2.0
component: Carbamoyl-phosphate synthase large chain, chloroplastic
component: Carbamoyl-phosphate synthase small chain, chloroplastic

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

argininosuccinate synthase
type: Complex
component stoichiometry: Protein/11067/Stoichiometry/4.0
component: Argininosuccinate synthase, chloroplastic

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

Reference/CAS 1188-37-0
type: UnificationXref
id: 1188-37-0
db: CAS

Reaction2721
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001415/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001003/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: L-Glutamic γ-semialdehyde
spontaneous: true
left: Water
left: 1-Pyrroline-5-carboxylic acid
left: Hydrogen Ion
name: 1-Pyrroline-5-carboxylic acid + Hydrogen Ion + Water → L-Glutamic γ-semialdehyde
conversion direction: LEFT_TO_RIGHT

Reference/UniProt Q42601
type: UnificationXref
id: Q42601
db: UniProt

Reaction2717
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001415/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001003/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Water
right: 1-Pyrroline-5-carboxylic acid
right: Hydrogen Ion
spontaneous: false
left: L-Glutamic γ-semialdehyde
name: L-Glutamic γ-semialdehyde → 1-Pyrroline-5-carboxylic acid + Hydrogen Ion + Water
conversion direction: LEFT_TO_RIGHT

Proline dehydrogenase 2, mitochondrial
type: ProteinReference
xref: Reference/UniProt Q6NKX1

acetylornithine deacetylase
type: Complex
component stoichiometry: Protein/11074/Stoichiometry/2.0
component: Acetylornithine deacetylase

Adenosine diphosphate
type: SmallMolecule
entity reference: Adenosine diphosphate

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

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

Reference/ChemSpider 16059
type: UnificationXref
id: 16059
db: ChemSpider

Reference/CAS 147-85-3
type: UnificationXref
id: 147-85-3
db: CAS

Compound/PW C000396/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Arginine
stoichiometric coefficient: 1.0

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

ChemicalStructure/PW C000723
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CCCNC(N)=O)C(O)=O

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

ChemicalStructure/PW C000721
type: ChemicalStructure
structure format: SMILES

Reference/ChEBI CHEBI 15682
type: UnificationXref
id: CHEBI:15682
db: ChEBI

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

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

Reference/UniProt P46637
type: UnificationXref
id: P46637
db: UniProt

Reference/SMPDB SMP0002420
type: UnificationXref
id: SMP0002420
db: SMPDB

Compound/PW C001860/Stoichiometry/1.0
type: Stoichiometry
physical entity: Quinone
stoichiometric coefficient: 1.0

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

Reference/ChEBI CHEBI 16543
type: UnificationXref
id: CHEBI:16543
db: ChEBI

Reference/BioCyc CARBAMOYL-P
type: UnificationXref
id: CARBAMOYL-P
db: BioCyc

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

Coenzyme A
type: SmallMolecule
entity reference: Coenzyme A

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/ChEBI CHEBI 1372
type: UnificationXref
id: CHEBI:1372
db: ChEBI

ChemicalStructure/PW C000862
type: ChemicalStructure
structure format: SMILES
structure data: NC(=O)OP(O)(O)=O

Reference/HMDB HMDB0006488
type: UnificationXref
id: HMDB0006488
db: HMDB

Compound/PW C000140/Stoichiometry/1.0
type: Stoichiometry
physical entity: Ornithine
stoichiometric coefficient: 1.0

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

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

Reference/ChEBI CHEBI 16878
type: UnificationXref
id: CHEBI:16878
db: ChEBI

Arabidopsis thaliana
type: BioSource
xref: Reference/TAXONOMY 3702

ChemicalStructure/PW C000940
type: ChemicalStructure
structure format: SMILES

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

Protein/11065/Stoichiometry/2.0
type: Stoichiometry
physical entity: Carbamoyl-phosphate synthase large chain, chloroplastic
stoichiometric coefficient: 2.0

Compound/PW C000723/Stoichiometry/1.0
type: Stoichiometry
physical entity: Citrulline
stoichiometric coefficient: 1.0

Reference/PubChem-compound 28782
type: UnificationXref
id: 28782
db: PubChem-compound

Reference/ChEBI CHEBI 16509
type: UnificationXref
id: CHEBI:16509
db: ChEBI

L-Glutamic acid
type: SmallMoleculeReference
xref: Reference/PubChem-compound 33032
xref: Reference/ChEBI CHEBI 16015
xref: Reference/ChemSpider 30572
xref: Reference/HMDB HMDB0000148
xref: Reference/CAS 56-86-0
xref: Reference/BioCyc GLT
xref: Reference/KEGG Compound C00025
chemical formula: C5H9NO4
molecular weight: 147.05316
structure: ChemicalStructure/PW C000095

Reference/PubChem-compound 33032
type: UnificationXref
id: 33032
db: PubChem-compound

Reference/KEGG Compound C00624
type: UnificationXref
id: C00624
db: KEGG Compound

Reference/ChemSpider 4489
type: UnificationXref
id: 4489
db: ChemSpider

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

Reference/UniProt Q940M2
type: UnificationXref
id: Q940M2
db: UniProt

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

Compound/PW C000134/Stoichiometry/1.0
type: Stoichiometry
physical entity: Oxoglutaric acid
stoichiometric coefficient: 1.0

Reference/BioCyc CPD-8130
type: UnificationXref
id: CPD-8130
db: BioCyc

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

Reference/CAS 123-31-9
type: UnificationXref
id: 123-31-9
db: CAS

Reference/BioCyc N-ALPHA-ACETYLORNITHINE
type: UnificationXref
id: N-ALPHA-ACETYLORNITHINE
db: BioCyc

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

Reference/ChEBI CHEBI 17544
type: UnificationXref
id: CHEBI:17544
db: ChEBI

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

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

ChemicalStructure/PW C000888
type: ChemicalStructure
structure format: SMILES
structure data: CC(=O)N[C@@H](CCC(O)=O)C(O)=O

ChemicalStructure/PW C001856
type: ChemicalStructure
structure format: SMILES
structure data: CC(=O)N[C@@H](CCCN)C(O)=O

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

Reference/PubChem-compound 1176
type: UnificationXref
id: 1176
db: PubChem-compound

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

Reference/PubChem-compound 439232
type: UnificationXref
id: 439232
db: PubChem-compound

ChemicalStructure/PW C001860
type: ChemicalStructure
structure format: SMILES
structure data: O=C1C=CC(=O)C=C1

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

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

Reference/PubChem-compound 278
type: UnificationXref
id: 278
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+]

Reference/ChEBI CHEBI 16467
type: UnificationXref
id: CHEBI:16467
db: ChEBI

Reference/ChEBI CHEBI 16349
type: UnificationXref
id: CHEBI:16349
db: ChEBI

Reference/BioCyc N-ACETYL-GLUTAMYL-P
type: UnificationXref
id: N-ACETYL-GLUTAMYL-P
db: BioCyc

ChemicalStructure/PW C000414
type: ChemicalStructure
structure format: SMILES

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

Reference/ChEBI CHEBI 17672
type: UnificationXref
id: CHEBI:17672
db: ChEBI

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

ChemicalStructure/PW C001632
type: ChemicalStructure
structure format: SMILES
structure data: OC1=CC=C(O)C=C1

Reference/ChemSpider 167387
type: UnificationXref
id: 167387
db: ChemSpider

Reference/ChemSpider 389220
type: UnificationXref
id: 389220
db: ChemSpider

Reference/PubChem-compound 185
type: UnificationXref
id: 185
db: PubChem-compound

ChemicalStructure/PW C000500
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CCC(N)=O)C(O)=O

Reference/PubChem-compound 1196
type: UnificationXref
id: 1196
db: PubChem-compound

Reference/KEGG Compound C00530
type: UnificationXref
id: C00530
db: KEGG Compound

Protein/11066/Stoichiometry/2.0
type: Stoichiometry
physical entity: Carbamoyl-phosphate synthase small chain, chloroplastic
stoichiometric coefficient: 2.0

Compound/PW C040034/Stoichiometry/2.0
type: Stoichiometry
physical entity: Hydrogen Ion
stoichiometric coefficient: 2.0

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

Reference/UniProt Q9M8M7
type: UnificationXref
id: Q9M8M7
db: UniProt

Reference/CAS 74-79-3
type: UnificationXref
id: 74-79-3
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Reference/CAS 106-51-4
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Reference/HMDB HMDB0000517
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Reference/ChEBI CHEBI 15351
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Reference/PubChem-compound 440236
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Reference/PubChem-compound 176
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Reference/HMDB HMDB0000641
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Reference/CAS 2906-39-0
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Reference/ChEBI CHEBI 16319
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Reference/CAS 85-61-0
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Reference/BioCyc L-ORNITHINE
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Reference/PathWhiz PW002526
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Reference/ChemSpider 180
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