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

Reference/UniProt Q8RY79
type: UnificationXref
id: Q8RY79
db: UniProt

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

Reference/CAS 7722-84-1
type: UnificationXref
id: 7722-84-1
db: CAS

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

Reference/BioCyc CPD-7650
type: UnificationXref
id: CPD-7650
db: BioCyc

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

Tyrosine aminotransferase
type: Protein
cellular location: Cytosol
entity reference: Tyrosine aminotransferase

Reference/PubChem-compound 5610
type: UnificationXref
id: 5610
db: PubChem-compound

Reference/ChEBI CHEBI 16134
type: UnificationXref
id: CHEBI:16134
db: ChEBI

Reference/BioCyc P-HYDROXY-PHENYLPYRUVATE
type: UnificationXref
id: P-HYDROXY-PHENYLPYRUVATE
db: BioCyc

Reference/UniProt Q9LVY1
type: UnificationXref
id: Q9LVY1
db: UniProt

Dopamine
type: SmallMolecule
entity reference: Dopamine
name: SubPathwayInput

Reference/HMDB HMDB0003125
type: UnificationXref
id: HMDB0003125
db: HMDB

Compound/PW C000103 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Tyrosine
stoichiometric coefficient: 1.0

Compound/PW C001065/Stoichiometry/1.0
type: Stoichiometry
physical entity: Oxygen
stoichiometric coefficient: 1.0

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

ChemicalStructure/PW C001783
type: ChemicalStructure
structure format: SMILES
structure data: OO

ChemicalStructure/PW C000210
type: ChemicalStructure
structure format: SMILES
structure data: NCCC1=CC=C(O)C=C1

Ammonia
type: SmallMoleculeReference
xref: Reference/BioCyc AMMONIA
xref: Reference/CAS 7664-41-7
xref: Reference/HMDB HMDB0000051
xref: Reference/PubChem-compound 222
xref: Reference/KEGG Compound C00014
xref: Reference/ChEBI CHEBI 16134
xref: Reference/ChemSpider 217
chemical formula: H3N
molecular weight: 17.026548
structure: ChemicalStructure/PW C000035

L-Tyrosine
type: SmallMolecule
cellular location: Cytosol
entity reference: L-Tyrosine

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

Reference/ChemSpider 5833
type: UnificationXref
id: 5833
db: ChemSpider

ChemicalStructure/PW C000103
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CC1=CC=C(O)C=C1)C(O)=O

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

Compound/PW C000103 Cytoplasm/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Tyrosine
stoichiometric coefficient: 1.0

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

Compound/PW C000035/Stoichiometry/1.0
type: Stoichiometry
physical entity: Ammonia
stoichiometric coefficient: 1.0

Compound/PW C000558 Cytoplasm/Stoichiometry/1.0
type: Stoichiometry
physical entity: 4-Hydroxyphenylpyruvic acid
stoichiometric coefficient: 1.0

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

Reference/HMDB HMDB0000306
type: UnificationXref
id: HMDB0000306
db: HMDB

Reference/ChemSpider 954
type: UnificationXref
id: 954
db: ChemSpider

Reference/PubChem-compound 6047
type: UnificationXref
id: 6047
db: PubChem-compound

Reference/ChemSpider 952
type: UnificationXref
id: 952
db: ChemSpider

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

Ammonia
type: SmallMolecule
entity reference: Ammonia

Reference/ChemSpider 274
type: UnificationXref
id: 274
db: ChemSpider

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/BioCyc TYR
type: UnificationXref
id: TYR
db: BioCyc

ChemicalStructure/PW C000558
type: ChemicalStructure
structure format: SMILES
structure data: OC(=O)C(=O)CC1=CC=C(O)C=C1

Primary amine oxidase 1
type: Protein
entity reference: Primary amine oxidase 1

Reference/ChEBI CHEBI 16240
type: UnificationXref
id: CHEBI:16240
db: ChEBI

Tyrosine decarboxylase 1
type: Protein
entity reference: Tyrosine decarboxylase 1

Reference/PubChem-compound 119219
type: UnificationXref
id: 119219
db: PubChem-compound

Reference/ChemSpider 5408
type: UnificationXref
id: 5408
db: ChemSpider

Reference/ChEBI CHEBI 15765
type: UnificationXref
id: CHEBI:15765
db: ChEBI

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

L-Glutamic acid
type: SmallMolecule
cellular location: Cytoplasm
entity reference: L-Glutamic acid

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

Reference/BioCyc CPD-6641
type: UnificationXref
id: CPD-6641
db: BioCyc

Reference/PubChem-compound 681
type: UnificationXref
id: 681
db: PubChem-compound

Reference/ChemSpider 217
type: UnificationXref
id: 217
db: ChemSpider

Reference/KEGG Compound C00355
type: UnificationXref
id: C00355
db: KEGG Compound

Reference/ChEBI CHEBI 15760
type: UnificationXref
id: CHEBI:15760
db: ChEBI

Reference/KEGG Compound C04043
type: UnificationXref
id: C04043
db: KEGG Compound

Protein/13579/Stoichiometry/2.0
type: Stoichiometry
physical entity: Primary amine oxidase 1
stoichiometric coefficient: 2.0

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

Oxygen
type: SmallMolecule
entity reference: Oxygen

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

Reference/CAS 124-38-9
type: UnificationXref
id: 124-38-9
db: CAS

Reference/KEGG Compound C00007
type: UnificationXref
id: C00007
db: KEGG Compound

Reference/KEGG Compound C03758
type: UnificationXref
id: C03758
db: KEGG Compound

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

ReactionCatalysis98527
type: Catalysis
controller: Tyrosine decarboxylase
controlled: Reaction108416
control type: ACTIVATION

ReactionCatalysis98528
type: Catalysis
controller: Primary amine oxidase
controlled: 1.4.3.21
control type: ACTIVATION

ReactionCatalysis98525
type: Catalysis
controller: Tyrosine aminotransferase
controlled: Reaction108414
control type: ACTIVATION

Reference/KEGG Compound C00483
type: UnificationXref
id: C00483
db: KEGG Compound

ReactionCatalysis98526
type: Catalysis
controller: Tyrosine decarboxylase
controlled: 4.1.1.25
control type: ACTIVATION

4-Hydroxyphenylpyruvic acid
type: SmallMolecule
cellular location: Cytoplasm
entity reference: 4-Hydroxyphenylpyruvic acid

Reference/ChEBI CHEBI 18243
type: UnificationXref
id: CHEBI:18243
db: ChEBI

Compound/PW C000117/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Dopa
stoichiometric coefficient: 1.0

3,4-Dihydroxyphenylacetaldehyde
type: SmallMoleculeReference
xref: Reference/KEGG Compound C04043
xref: Reference/ChemSpider 106504
xref: Reference/PubChem-compound 119219
xref: Reference/ChEBI CHEBI 27978
xref: Reference/CAS 5707-55-1
xref: Reference/HMDB HMDB0003791
chemical formula: C8H8O3
molecular weight: 152.04735
structure: ChemicalStructure/PW C001969

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

Reference/CAS 7664-41-7
type: UnificationXref
id: 7664-41-7
db: CAS

Oxoglutaric acid
type: SmallMolecule
cellular location: Cytosol
entity reference: Oxoglutaric acid

3,4-Dihydroxyphenylacetaldehyde
type: SmallMolecule
entity reference: 3,4-Dihydroxyphenylacetaldehyde

Reference/CAS 51-67-2
type: UnificationXref
id: 51-67-2
db: CAS

Compound/PW C001783/Stoichiometry/1.0
type: Stoichiometry
physical entity: Hydrogen peroxide
stoichiometric coefficient: 1.0

Reference/KEGG Compound C00011
type: UnificationXref
id: C00011
db: KEGG Compound

ChemicalStructure/PW C001316
type: ChemicalStructure
structure format: SMILES
structure data: O=C=O

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

L-Tyrosine
type: SmallMolecule
cellular location: Cytoplasm
entity reference: L-Tyrosine

Reference/PubChem-compound 222
type: UnificationXref
id: 222
db: PubChem-compound

Reference/KEGG Compound C00014
type: UnificationXref
id: C00014
db: KEGG Compound

Reference/ChEBI CHEBI 27978
type: UnificationXref
id: CHEBI:27978
db: ChEBI

Compound/PW C000210/Stoichiometry/1.0
type: Stoichiometry
physical entity: Tyramine
stoichiometric coefficient: 1.0

Dopamine
type: SmallMoleculeReference
xref: Reference/CAS 51-61-6
xref: Reference/KEGG Compound C03758
xref: Reference/ChemSpider 661
xref: Reference/BioCyc DOPAMINE
xref: Reference/HMDB HMDB0000073
xref: Reference/PubChem-compound 681
xref: Reference/ChEBI CHEBI 18243
chemical formula: C8H11NO2
molecular weight: 153.07898
structure: ChemicalStructure/PW C000052

Reference/ChEBI CHEBI 15999
type: UnificationXref
id: CHEBI:15999
db: ChEBI

ChemicalStructure/PW C000117
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CC1=CC=C(O)C(O)=C1)C(O)=O

Isoquinoline Alkaloid Biosynthesis
type: Pathway
pathway order: PathwaySubPathway/57048
pathway order: PathwaySubPathway/57047
pathway order: PathwayEnzymeReaction/1188955
pathway order: PathwayEnzymeReaction/1188924
pathway order: PathwayEnzymeReaction/1188979
pathway order: PathwayEnzymeReaction/1188978
pathway order: PathwayEnzymeReaction/1188925
pathway component: 1.4.3.21
pathway component: Phenylalanine, tyrosine and tryptophan biosynthesis
pathway component: Tyrosine metabolism
pathway component: ReactionCatalysis98527
pathway component: ReactionCatalysis98528
pathway component: ReactionCatalysis98525
pathway component: ReactionCatalysis98526
pathway component: Reaction108414
pathway component: ReactionCatalysis98546
pathway component: 4.1.1.25
pathway component: Reaction108416
xref: Reference/SMPDB SMP0063471
xref: Reference/PathWhiz PW064433
organism: Arabidopsis thaliana

L-Glutamic acid
type: SmallMolecule
cellular location: Cytosol
entity reference: L-Glutamic acid

Reference/KEGG Compound C00027
type: UnificationXref
id: C00027
db: KEGG Compound

ReactionCatalysis98546
type: Catalysis
controller: Aspartate aminotransferase, cytoplasmic
controlled: Reaction108414
control type: ACTIVATION

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

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

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

Compound/PW C000103/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Tyrosine
stoichiometric coefficient: 1.0

SubPathwayInteraction57047
type: Interaction
name: SubPathway57047Reaction
name: SubPathwayReaction
participant: L-Tyrosine

Reference/UniProt O23349
type: UnificationXref
id: O23349
db: UniProt

Reference/CAS 5707-55-1
type: UnificationXref
id: 5707-55-1
db: CAS

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

Water
type: SmallMolecule
entity reference: Water

Hydrogen peroxide
type: SmallMolecule
entity reference: Hydrogen peroxide

ChemicalStructure/PW C000052
type: ChemicalStructure
structure format: SMILES
structure data: NCCC1=CC(O)=C(O)C=C1

Tyramine
type: SmallMolecule
entity reference: Tyramine

Reference/BioCyc HYDROGEN-PEROXIDE
type: UnificationXref
id: HYDROGEN-PEROXIDE
db: BioCyc

SubPathwayInteraction57048
type: Interaction
name: SubPathwayReaction
name: SubPathway57048Reaction
participant: Dopamine

Phenylalanine, tyrosine and tryptophan biosynthesis
type: Pathway
pathway order: SubPathwayInteractionSteps/SubPathway57047
pathway component: SubPathwayInteraction57047
name: SubPathway

4-Hydroxyphenylpyruvic acid
type: SmallMoleculeReference
xref: Reference/BioCyc P-HYDROXY-PHENYLPYRUVATE
xref: Reference/CAS 156-39-8
xref: Reference/ChEBI CHEBI 15999
xref: Reference/PubChem-compound 979
xref: Reference/HMDB HMDB0000707
xref: Reference/ChemSpider 954
xref: Reference/KEGG Compound C01179
chemical formula: C9H8O4
molecular weight: 180.04225
structure: ChemicalStructure/PW C000558

Tyrosine metabolism
type: Pathway
pathway order: SubPathwayInteractionSteps/SubPathway57048
pathway component: SubPathwayInteraction57048
name: SubPathway

Tyrosine decarboxylase
type: Complex
component stoichiometry: Protein/13578/Stoichiometry/2.0
component: Tyrosine decarboxylase 1

Aspartate aminotransferase, cytoplasmic
type: Complex
cellular location: Cytoplasm
component: Aspartate aminotransferase, cytoplasmic isozyme 2
component: Aspartate aminotransferase, cytoplasmic isozyme 1

Reference/UniProt P46646
type: UnificationXref
id: P46646
db: UniProt

Reference/ChemSpider 763
type: UnificationXref
id: 763
db: ChemSpider

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

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

Reference/CAS 59-92-7
type: UnificationXref
id: 59-92-7
db: CAS

Reference/UniProt P46645
type: UnificationXref
id: P46645
db: UniProt

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

Tyrosine aminotransferase
type: ProteinReference
xref: Reference/UniProt Q9LVY1
organism: Arabidopsis thaliana

Tyrosine decarboxylase 1
type: ProteinReference
xref: Reference/UniProt Q8RY79
organism: Arabidopsis thaliana

Reference/PubChem-compound 784
type: UnificationXref
id: 784
db: PubChem-compound

Reference/CAS 51-61-6
type: UnificationXref
id: 51-61-6
db: CAS

Reference/ChemSpider 106504
type: UnificationXref
id: 106504
db: ChemSpider

Arabidopsis thaliana
type: BioSource
xref: Reference/TAXONOMY 3702

Reference/HMDB HMDB0000707
type: UnificationXref
id: HMDB0000707
db: HMDB

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

Reference/PathWhiz PW064433
type: UnificationXref
id: PW064433
db: PathWhiz

4-Hydroxyphenylpyruvic acid
type: SmallMolecule
cellular location: Cytosol
entity reference: 4-Hydroxyphenylpyruvic acid

Reference/HMDB HMDB0000158
type: UnificationXref
id: HMDB0000158
db: HMDB

Oxygen
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0001377
xref: Reference/ChemSpider 952
xref: Reference/KEGG Compound C00007
xref: Reference/ChEBI CHEBI 15379
xref: Reference/PubChem-compound 977
xref: Reference/BioCyc CPD-6641
xref: Reference/CAS 7782-44-7
chemical formula: O2
molecular weight: 31.98983
structure: ChemicalStructure/PW C001065

Compound/PW C001316/Stoichiometry/1.0
type: Stoichiometry
physical entity: Carbon dioxide
stoichiometric coefficient: 1.0

Aspartate aminotransferase, cytoplasmic isozyme 1
type: Protein
cellular location: Cytoplasm
entity reference: Aspartate aminotransferase, cytoplasmic isozyme 1

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

ChemicalStructure/PW C000035
type: ChemicalStructure
structure format: SMILES
structure data: N

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

Primary amine oxidase
type: Complex
component stoichiometry: Protein/13579/Stoichiometry/2.0
component: Primary amine oxidase 1

Primary amine oxidase 1
type: ProteinReference
xref: Reference/UniProt O23349
organism: Arabidopsis thaliana

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/SMPDB SMP0063471
type: UnificationXref
id: SMP0063471
db: SMPDB

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

1.4.3.21
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001065/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001783/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001969/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000052/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000035/Stoichiometry/1.0
right: Hydrogen peroxide
right: 3,4-Dihydroxyphenylacetaldehyde
right: Ammonia
spontaneous: false
EC number: 1.4.3.21
left: Dopamine
left: Water
left: Oxygen
name: Dopamine + Oxygen + Water → 3,4-Dihydroxyphenylacetaldehyde + Ammonia + Hydrogen peroxide
conversion direction: LEFT_TO_RIGHT

Reference/CAS 60-18-4
type: UnificationXref
id: 60-18-4
db: CAS

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

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

Reference/ChEBI CHEBI 16526
type: UnificationXref
id: CHEBI:16526
db: ChEBI

Reaction108414
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000558 Cytoplasm/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000103 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000134 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000103 Cytoplasm/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000095 Cytoplasm/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000095 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000134 Cytoplasm/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000558 Cytosol/Stoichiometry/1.0
right: 4-Hydroxyphenylpyruvic acid
right: L-Glutamic acid
spontaneous: false
left: Oxoglutaric acid
left: L-Tyrosine
name: L-Tyrosine + Oxoglutaric acid → 4-Hydroxyphenylpyruvic acid + L-Glutamic acid
conversion direction: LEFT_TO_RIGHT

4.1.1.25
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001316/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000210/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000103/Stoichiometry/1.0
right: Tyramine
right: Carbon dioxide
spontaneous: false
EC number: 4.1.1.25
left: L-Tyrosine
name: L-Tyrosine → Carbon dioxide + Tyramine
conversion direction: LEFT_TO_RIGHT

Reference/CAS 7782-44-7
type: UnificationXref
id: 7782-44-7
db: CAS

Reaction108416
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001316/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000117/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000052/Stoichiometry/1.0
right: Dopamine
right: Carbon dioxide
spontaneous: false
left: L-Dopa
name: L-Dopa → Carbon dioxide + Dopamine
conversion direction: LEFT_TO_RIGHT

Reference/HMDB HMDB0001377
type: UnificationXref
id: HMDB0001377
db: HMDB

Reference/ChemSpider 661
type: UnificationXref
id: 661
db: ChemSpider

Reference/HMDB HMDB0003791
type: UnificationXref
id: HMDB0003791
db: HMDB

Compound/PW C001969/Stoichiometry/1.0
type: Stoichiometry
physical entity: 3,4-Dihydroxyphenylacetaldehyde
stoichiometric coefficient: 1.0

Compound/PW C000052/Stoichiometry/1.0
type: Stoichiometry
physical entity: Dopamine
stoichiometric coefficient: 1.0

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

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

L-Tyrosine
type: SmallMoleculeReference
xref: Reference/CAS 60-18-4
xref: Reference/PubChem-compound 6057
xref: Reference/HMDB HMDB0000158
xref: Reference/ChEBI CHEBI 17895
xref: Reference/KEGG Compound C00082
xref: Reference/ChemSpider 5833
xref: Reference/BioCyc TYR
chemical formula: C9H11NO3
molecular weight: 181.0739
structure: ChemicalStructure/PW C000103

Carbon dioxide
type: SmallMoleculeReference
xref: Reference/PubChem-compound 280
xref: Reference/ChEBI CHEBI 16526
xref: Reference/ChemSpider 274
xref: Reference/HMDB HMDB0001967
xref: Reference/CAS 124-38-9
xref: Reference/KEGG Compound C00011
chemical formula: CO2
molecular weight: 43.98983
structure: ChemicalStructure/PW C001316

ChemicalStructure/PW C001065
type: ChemicalStructure
structure format: SMILES
structure data: O=O

Reference/KEGG Compound C00082
type: UnificationXref
id: C00082
db: KEGG Compound

Oxoglutaric acid
type: SmallMolecule
cellular location: Cytoplasm
entity reference: Oxoglutaric acid

Reference/HMDB HMDB0000051
type: UnificationXref
id: HMDB0000051
db: HMDB

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

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

Reference/PubChem-compound 6057
type: UnificationXref
id: 6057
db: PubChem-compound

Reference/ChEBI CHEBI 15379
type: UnificationXref
id: CHEBI:15379
db: ChEBI

L-Dopa
type: SmallMoleculeReference
xref: Reference/ChemSpider 5824
xref: Reference/CAS 59-92-7
xref: Reference/ChEBI CHEBI 15765
xref: Reference/HMDB HMDB0000181
xref: Reference/BioCyc L-DOPA
xref: Reference/KEGG Compound C00355
xref: Reference/PubChem-compound 6047
chemical formula: C9H11NO4
molecular weight: 197.0688
structure: ChemicalStructure/PW C000117

Reference/KEGG Compound C01179
type: UnificationXref
id: C01179
db: KEGG Compound

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

Reference/PubChem-compound 280
type: UnificationXref
id: 280
db: PubChem-compound

Aspartate aminotransferase, cytoplasmic isozyme 1
type: ProteinReference
xref: Reference/UniProt P46645
organism: Arabidopsis thaliana

Reference/HMDB HMDB0000181
type: UnificationXref
id: HMDB0000181
db: HMDB

Protein/13578/Stoichiometry/2.0
type: Stoichiometry
physical entity: Tyrosine decarboxylase 1
stoichiometric coefficient: 2.0

Reference/ChemSpider 5824
type: UnificationXref
id: 5824
db: ChemSpider

Reference/CAS 156-39-8
type: UnificationXref
id: 156-39-8
db: CAS

Aspartate aminotransferase, cytoplasmic isozyme 2
type: Protein
cellular location: Cytoplasm
entity reference: Aspartate aminotransferase, cytoplasmic isozyme 2

Aspartate aminotransferase, cytoplasmic isozyme 2
type: ProteinReference
xref: Reference/UniProt P46646
organism: Arabidopsis thaliana

L-Dopa
type: SmallMolecule
entity reference: L-Dopa

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

Hydrogen peroxide
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0003125
xref: Reference/PubChem-compound 784
xref: Reference/ChemSpider 763
xref: Reference/CAS 7722-84-1
xref: Reference/BioCyc HYDROGEN-PEROXIDE
xref: Reference/ChEBI CHEBI 16240
xref: Reference/KEGG Compound C00027
chemical formula: H2O2
molecular weight: 34.005478
structure: ChemicalStructure/PW C001783

Reference/HMDB HMDB0000073
type: UnificationXref
id: HMDB0000073
db: HMDB

Tyramine
type: SmallMoleculeReference
xref: Reference/ChemSpider 5408
xref: Reference/CAS 51-67-2
xref: Reference/BioCyc CPD-7650
xref: Reference/HMDB HMDB0000306
xref: Reference/KEGG Compound C00483
xref: Reference/PubChem-compound 5610
xref: Reference/ChEBI CHEBI 15760
chemical formula: C8H11NO
molecular weight: 137.08406
structure: ChemicalStructure/PW C000210

Compound/PW C000558 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: 4-Hydroxyphenylpyruvic acid
stoichiometric coefficient: 1.0

Reference/ChEBI CHEBI 17895
type: UnificationXref
id: CHEBI:17895
db: ChEBI

Reference/PubChem-compound 977
type: UnificationXref
id: 977
db: PubChem-compound

Carbon dioxide
type: SmallMolecule
entity reference: Carbon dioxide

Reference/HMDB HMDB0001967
type: UnificationXref
id: HMDB0001967
db: HMDB

L-Tyrosine
type: SmallMolecule
entity reference: L-Tyrosine
name: SubPathwayOutput

ChemicalStructure/PW C001969
type: ChemicalStructure
structure format: SMILES
structure data: OC1=C(O)C=C(CC=O)C=C1

Reference/PubChem-compound 979
type: UnificationXref
id: 979
db: PubChem-compound