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

Reference/CAS 61-54-1
type: UnificationXref
id: 61-54-1
db: CAS

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

Reference/PubChem-compound 800
type: UnificationXref
id: 800
db: PubChem-compound

Hydrogen Ion
type: SmallMolecule
cellular location: Peroxisome
entity reference: Hydrogen Ion

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

Reference/HMDB HMDB0012199
type: UnificationXref
id: HMDB0012199
db: HMDB

ReactionCatalysis7309
type: Catalysis
controller: Abscisic-aldehyde oxidase
controlled: 1.2.3.14,1.2.3.7
control type: ACTIVATION

ReactionCatalysis7308
type: Catalysis
controller: Anthranilate synthase
controlled: 4.1.3.27
control type: ACTIVATION

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

Neoglucobrassicin
type: SmallMolecule
cellular location: Endoplasmic Reticulum
entity reference: Neoglucobrassicin

Reference/HMDB HMDB0001185
type: UnificationXref
id: HMDB0001185
db: HMDB

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

Reference/ChemSpider 58238
type: UnificationXref
id: 58238
db: ChemSpider

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

Reference/ChemSpider 1118
type: UnificationXref
id: 1118
db: ChemSpider

Reference/HMDB HMDB0001190
type: UnificationXref
id: HMDB0001190
db: HMDB

Pyruvic acid
type: SmallMolecule
cellular location: Chloroplast
entity reference: Pyruvic acid

N,N-dihydroxy-L-tryptophan
type: SmallMolecule
cellular location: Cytosol
entity reference: N,N-dihydroxy-L-tryptophan

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

Reference/ChEBI CHEBI 17111
type: UnificationXref
id: CHEBI:17111
db: ChEBI

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

ReactionCatalysis7319
type: Catalysis
controller: UDP-glycosyltransferase 74B1
controlled: 2.4.1.-,2.4.1.195
control type: ACTIVATION

ReactionCatalysis7318
type: Catalysis
controller: S-alkyl-thiohydroximate lyase SUR1
controlled: 4.4.1.-
control type: ACTIVATION

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

ReactionCatalysis7313
type: Catalysis
controller: Tryptophan N-monooxygenase
controlled: Reaction7345
control type: ACTIVATION

ReactionCatalysis7317
type: Catalysis
controller: Cytochrome P450 83B1
controlled: 1.14.-.-
control type: ACTIVATION

ReactionCatalysis7316
type: Catalysis
controller: Tryptophan N-monooxygenase
controlled: Reaction7348
control type: ACTIVATION

ReactionCatalysis7315
type: Catalysis
controller: Tryptophan N-monooxygenase
controlled: Reaction7347
control type: ACTIVATION

S-Adenosylmethionine
type: SmallMoleculeReference
xref: Reference/PubChem-compound 24762165
xref: Reference/KEGG Compound C00019
xref: Reference/ChemSpider 31983
xref: Reference/ChEBI CHEBI 15414
xref: Reference/CAS 485-80-3
xref: Reference/BioCyc S-ADENOSYLMETHIONINE
xref: Reference/HMDB HMDB0001185
chemical formula: C15H23N6O5S
molecular weight: 399.14505
structure: ChemicalStructure/PW C000921

ReactionCatalysis7320
type: Catalysis
controller: Cytosolic sulfotransferase 18
controlled: 2.8.2.-
control type: ACTIVATION

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

S-alkyl-thiohydroximate lyase SUR1
type: Protein
cellular location: Cytosol
entity reference: S-alkyl-thiohydroximate lyase SUR1

Compound/PW C000921 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: S-Adenosylmethionine
stoichiometric coefficient: 1.0

Indoleacetaldehyde
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0001190
xref: Reference/KEGG Compound C00637
xref: Reference/PubChem-compound 800
xref: Reference/CAS 2591-98-2
xref: Reference/ChEBI CHEBI 18086
xref: Reference/ChemSpider 778
xref: Reference/BioCyc INDOLE ACETALDEHYDE
chemical formula: C10H9NO
molecular weight: 159.06842
structure: ChemicalStructure/PW C000926

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

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

Compound/PW C045260 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: (Z)-indol-3-ylacetaldoxime
stoichiometric coefficient: 1.0

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

ChemicalStructure/PW C007748
type: ChemicalStructure
structure format: SMILES

Reference/PubChem-compound 14524362
type: UnificationXref
id: 14524362
db: PubChem-compound

Reference/CAS 7540-64-9
type: UnificationXref
id: 7540-64-9
db: CAS

Reference/GENE ONTOLOGY GO 0009507
type: UnificationXref
id: GO:0009507
db: GENE ONTOLOGY

Compound/PW C011457/Stoichiometry/1.0
type: Stoichiometry
physical entity: Glucobrassicin
stoichiometric coefficient: 1.0

ReactionCatalysis7324
type: Catalysis
controller: Cytochrome P450 81F3
controlled: 1.14.-.-
control type: ACTIVATION

ReactionCatalysis7323
type: Catalysis
controller: Cytochrome P450 81F4
controlled: 1.14.-.-
control type: ACTIVATION

ReactionCatalysis7322
type: Catalysis
controller: Beta-glucosidase 26, peroxisomal
controlled: 3.2.1.21
control type: ACTIVATION

ChemicalStructure/PW C042673
type: ChemicalStructure
structure format: SMILES

Compound/PW C007748 Chloroplast/Stoichiometry/1.0
type: Stoichiometry
physical entity: Chorismate
stoichiometric coefficient: 1.0

ReactionCatalysis7321
type: Catalysis
controller: Cytosolic sulfotransferase 16
controlled: 2.8.2.-
control type: ACTIVATION

Reference/ChEBI CHEBI 1865
type: UnificationXref
id: CHEBI:1865
db: ChEBI

ReactionCatalysis7327
type: Catalysis
controller: Indole glucosinolate O-methyltransferase
controlled: 2.1.1.-
control type: ACTIVATION

ReactionCatalysis7326
type: Catalysis
controller: Cytochrome P450 81F1
controlled: 1.14.-.-
control type: ACTIVATION

ReactionCatalysis7325
type: Catalysis
controller: Cytochrome P450 81F2
controlled: 1.14.-.-
control type: ACTIVATION

Reference/KEGG Compound C00108
type: UnificationXref
id: C00108
db: KEGG Compound

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

Reference/PubChem-compound 53477679
type: UnificationXref
id: 53477679
db: PubChem-compound

Indoleglycerol phosphate
type: SmallMolecule
entity reference: Indoleglycerol phosphate

Reference/PubChem-compound 6031
type: UnificationXref
id: 6031
db: PubChem-compound

Reference/ChemSpider 709
type: UnificationXref
id: 709
db: ChemSpider

Reference/CAS 133-89-1
type: UnificationXref
id: 133-89-1
db: CAS

Reference/KEGG Compound C00463
type: UnificationXref
id: C00463
db: KEGG Compound

Reference/KEGG Compound C00221
type: UnificationXref
id: C00221
db: KEGG Compound

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

Reference/ChEBI CHEBI 17333
type: UnificationXref
id: CHEBI:17333
db: ChEBI

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

Cytosolic sulfotransferase 16
type: Protein
entity reference: Cytosolic sulfotransferase 16

Reference/CAS 73-22-3
type: UnificationXref
id: 73-22-3
db: CAS

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

Uridine 5'-diphosphate
type: SmallMolecule
cellular location: Cytosol
entity reference: Uridine 5'-diphosphate

Compound/PW C045261 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: indole-3-acetonitrile oxide
stoichiometric coefficient: 1.0

Indoleglycerol phosphate
type: SmallMoleculeReference
xref: Reference/PubChem-compound 46878464
chemical formula: C11H12NO6P
molecular weight: 285.04022
structure: ChemicalStructure/PW C044564

Reference/KEGG Compound C00119
type: UnificationXref
id: C00119
db: KEGG Compound

D-Glyceraldehyde 3-phosphate
type: SmallMoleculeReference
xref: Reference/BioCyc GAP
xref: Reference/ChEBI CHEBI 17138
xref: Reference/HMDB HMDB0001112
xref: Reference/ChemSpider 709
xref: Reference/KEGG Compound C00661
xref: Reference/PubChem-compound 729
xref: Reference/CAS 591-59-3
chemical formula: C3H7O6P
molecular weight: 169.99803
structure: ChemicalStructure/PW C000869

Reference/ChemSpider 83867
type: UnificationXref
id: 83867
db: ChemSpider

ChemicalStructure/PW C000926
type: ChemicalStructure
structure format: SMILES
structure data: O=CCC1=CNC2=C1C=CC=C2

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

Hydrogen Ion
type: SmallMolecule
entity reference: Hydrogen Ion

Compound/PW C000741/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Tryptophan
stoichiometric coefficient: 1.0

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

Reference/PubChem-compound 5459978
type: UnificationXref
id: 5459978
db: PubChem-compound

Water
type: SmallMolecule
cellular location: Peroxisome
entity reference: Water

Reference/HMDB HMDB0038384
type: UnificationXref
id: HMDB0038384
db: HMDB

L-Tryptophan
type: SmallMoleculeReference
xref: Reference/CAS 73-22-3
xref: Reference/KEGG Compound C00078
xref: Reference/ChEBI CHEBI 16828
xref: Reference/PubChem-compound 6305
xref: Reference/BioCyc TRP
xref: Reference/HMDB HMDB0000929
xref: Reference/ChemSpider 6066
chemical formula: C11H12N2O2
molecular weight: 204.08987
structure: ChemicalStructure/PW C000741

Reference/PubChem-compound 9601691
type: UnificationXref
id: 9601691
db: PubChem-compound

Glucobrassicin
type: SmallMolecule
cellular location: Peroxisome
entity reference: Glucobrassicin

Anthranilate phosphoribosyltransferase, chloroplastic
type: Protein
entity reference: Anthranilate phosphoribosyltransferase, chloroplastic

ChemicalStructure/PW C000921
type: ChemicalStructure
structure format: SMILES

Reference/CAS 979-92-0
type: UnificationXref
id: 979-92-0
db: CAS

N-(5'-phosphoribosyl)anthranilate isomerase 2, chloroplastic
type: Protein
entity reference: N-(5'-phosphoribosyl)anthranilate isomerase 2, chloroplastic

Reference/PubChem-compound 124886
type: UnificationXref
id: 124886
db: PubChem-compound

Tryptophan synthase beta chain 2, chloroplastic
type: Protein
entity reference: Tryptophan synthase beta chain 2, chloroplastic

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

Reference/UniProt Q9SIV0
type: UnificationXref
id: Q9SIV0
db: UniProt

S-Adenosylhomocysteine
type: SmallMoleculeReference
xref: Reference/PubChem-compound 25246222
xref: Reference/ChemSpider 388301
xref: Reference/BioCyc ADENOSYL-HOMO-CYS
xref: Reference/CAS 979-92-0
xref: Reference/KEGG Compound C00021
xref: Reference/ChEBI CHEBI 16680
xref: Reference/HMDB HMDB0000939
chemical formula: C14H20N6O5S
molecular weight: 384.12158
structure: ChemicalStructure/PW C000749

Reference/UniProt Q9LVD6
type: UnificationXref
id: Q9LVD6
db: UniProt

Cytochrome P450 81F2
type: Protein
cellular location: Cytosol
entity reference: Cytochrome P450 81F2

Reference/UniProt Q7G9P4
type: UnificationXref
id: Q7G9P4
db: UniProt

Glutathione
type: SmallMolecule
cellular location: Cytosol
entity reference: Glutathione

1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate
type: SmallMoleculeReference
chemical formula: C12H16NO9P
molecular weight: 349.05627
structure: ChemicalStructure/PW C042673

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

2-Aminobenzoic acid
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00108
xref: Reference/ChEBI CHEBI 30754
xref: Reference/HMDB HMDB0001123
xref: Reference/ChemSpider 222
xref: Reference/CAS 118-92-3
xref: Reference/PubChem-compound 227
xref: Reference/BioCyc ANTHRANILATE
chemical formula: C7H7NO2
molecular weight: 137.04768
structure: ChemicalStructure/PW C000877

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

Hydrogen Ion
type: SmallMolecule
cellular location: Cytosol
entity reference: Hydrogen Ion

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

Tryptophan N-monooxygenase
type: Complex
cellular location: Cytosol
component: Tryptophan N-monooxygenase 1
component: Tryptophan N-monooxygenase 2

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

Phosphoadenosine phosphosulfate
type: SmallMolecule
entity reference: Phosphoadenosine phosphosulfate

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

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

NADPH
type: SmallMolecule
cellular location: Cytosol
entity reference: NADPH

Compound/PW C045266 Peroxisome/Stoichiometry/1.0
type: Stoichiometry
physical entity: indolylmethyl glucosinolate aglycone
stoichiometric coefficient: 1.0

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

Compound/PW C000190/Stoichiometry/1.0
type: Stoichiometry
physical entity: Phosphoribosyl pyrophosphate
stoichiometric coefficient: 1.0

Compound/PW C000201 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Uridine 5'-diphosphate
stoichiometric coefficient: 1.0

Reference/UniProt O64883
type: UnificationXref
id: O64883
db: UniProt

Reference/KEGG Compound C00019
type: UnificationXref
id: C00019
db: KEGG Compound

indole-3-acetohydroximoyl-cysteinylglycine
type: SmallMolecule
cellular location: Cytosol
entity reference: indole-3-acetohydroximoyl-cysteinylglycine

Reference/UniProt Q9C9C9
type: UnificationXref
id: Q9C9C9
db: UniProt

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

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

Reference/PubChem-compound 7339
type: UnificationXref
id: 7339
db: PubChem-compound

Reference/KEGG Compound C00251
type: UnificationXref
id: C00251
db: KEGG Compound

Indoleacetaldehyde
type: SmallMolecule
cellular location: Cytosol
entity reference: Indoleacetaldehyde

Reference/KEGG Compound C00015
type: UnificationXref
id: C00015
db: KEGG Compound

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

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

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

Reference/PubChem-compound 7009644
type: UnificationXref
id: 7009644
db: PubChem-compound

Compound/PW C045259 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: (E)-indol-3-ylacetaldoxime
stoichiometric coefficient: 1.0

Reference/CAS 687-63-8
type: UnificationXref
id: 687-63-8
db: CAS

Reference/UniProt Q9C9D0
type: UnificationXref
id: Q9C9D0
db: UniProt

Reference/ChEBI CHEBI 17138
type: UnificationXref
id: CHEBI:17138
db: ChEBI

Hydrogen Ion
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00080
xref: Reference/ChEBI CHEBI 15378
xref: Reference/HMDB HMDB0059597
xref: Reference/PubChem-compound 1038
xref: Reference/ChemSpider 1010
chemical formula: H
molecular weight: 1.007825
structure: ChemicalStructure/PW C040034

Reference/KEGG Compound C00029
type: UnificationXref
id: C00029
db: KEGG Compound

Reference/ChemSpider 388301
type: UnificationXref
id: 388301
db: ChemSpider

D-Glyceraldehyde 3-phosphate
type: SmallMolecule
entity reference: D-Glyceraldehyde 3-phosphate

Cytochrome P450 81F4
type: Protein
cellular location: Endoplasmic Reticulum
entity reference: Cytochrome P450 81F4

Indole glucosinolate O-methyltransferase 2
type: Protein
cellular location: Cytosol
entity reference: Indole glucosinolate O-methyltransferase 2

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

Neoglucobrassicin
type: SmallMoleculeReference
xref: Reference/CAS 5187-84-8
xref: Reference/HMDB HMDB0038384
xref: Reference/ChEBI CHEBI 27506
xref: Reference/KEGG Compound C08424
chemical formula: C17H22N2O10S2
molecular weight: 478.0716
structure: ChemicalStructure/PW C019230

L-Tryptophan
type: SmallMolecule
entity reference: L-Tryptophan

Reference/KEGG Compound C00021
type: UnificationXref
id: C00021
db: KEGG Compound

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

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

Compound/PW C045267 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: 4-hydroxy-3-indolylmethyl-glucosinolate
stoichiometric coefficient: 1.0

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

indolylmethyl glucosinolate aglycone
type: SmallMolecule
cellular location: Peroxisome
entity reference: indolylmethyl glucosinolate aglycone

Reference/CAS 482-67-7
type: UnificationXref
id: 482-67-7
db: CAS

NADP
type: SmallMolecule
cellular location: Cytosol
entity reference: NADP

Compound/PW C045268 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: 4-methoxy-3-indolylmethyl-glucosinolate
stoichiometric coefficient: 1.0

Reference/BioCyc OXIDIZED-GLUTATHIONE
type: UnificationXref
id: OXIDIZED-GLUTATHIONE
db: BioCyc

Compound/PW C000528 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Indolelactic acid
stoichiometric coefficient: 1.0

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

Reference/ChemSpider 778
type: UnificationXref
id: 778
db: ChemSpider

Reference/ChEBI CHEBI 18277
type: UnificationXref
id: CHEBI:18277
db: ChEBI

Reference/KEGG Compound C00398
type: UnificationXref
id: C00398
db: KEGG Compound

Reference/ChemSpider 776
type: UnificationXref
id: 776
db: ChemSpider

Water
type: SmallMolecule
entity reference: Water

Peroxisome
type: CellularLocationVocabulary
xref: Reference/GENE ONTOLOGY GO 0005777

Reference/UniProt Q9LPU5
type: UnificationXref
id: Q9LPU5
db: UniProt

Reference/UniProt Q9LPU7
type: UnificationXref
id: Q9LPU7
db: UniProt

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

Reference/ChEBI CHEBI 58729
type: UnificationXref
id: CHEBI:58729
db: ChEBI

Reference/ChEBI CHEBI 58728
type: UnificationXref
id: CHEBI:58728
db: ChEBI

Reference/CAS 492-61-5
type: UnificationXref
id: 492-61-5
db: CAS

Reference/UniProt O65782
type: UnificationXref
id: O65782
db: UniProt

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/PubChem-compound 92904
type: UnificationXref
id: 92904
db: PubChem-compound

Compound/PW C000207 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Tryptamine
stoichiometric coefficient: 1.0

Compound/PW C010294 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Serylglycine
stoichiometric coefficient: 1.0

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

Compound/PW C044564/Stoichiometry/1.0
type: Stoichiometry
physical entity: Indoleglycerol phosphate
stoichiometric coefficient: 1.0

Reference/HMDB HMDB0001112
type: UnificationXref
id: HMDB0001112
db: HMDB

Reference/ChemSpider 7062
type: UnificationXref
id: 7062
db: ChemSpider

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

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

Compound/PW C000193 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Uridine diphosphate glucose
stoichiometric coefficient: 1.0

4-methoxy-3-indolylmethyl-glucosinolate
type: SmallMolecule
cellular location: Cytosol
entity reference: 4-methoxy-3-indolylmethyl-glucosinolate

Reference/UniProt Q9SZU1
type: UnificationXref
id: Q9SZU1
db: UniProt

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

Reference/KEGG Compound C00051
type: UnificationXref
id: C00051
db: KEGG Compound

Uridine 5'-diphosphate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 17659
xref: Reference/PubChem-compound 6031
xref: Reference/CAS 58-98-0
xref: Reference/HMDB HMDB0000295
xref: Reference/KEGG Compound C00015
xref: Reference/ChemSpider 5809
xref: Reference/BioCyc UDP
chemical formula: C9H14N2O12P2
molecular weight: 404.0022
structure: ChemicalStructure/PW C000201

Cytochrome P450 83B1
type: Protein
cellular location: Cytosol
entity reference: Cytochrome P450 83B1

Reaction6530
type: BiochemicalReaction
participant stoichiometry: Compound/PW C044564/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001316/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042673/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Water
right: Indoleglycerol phosphate
right: Carbon dioxide
spontaneous: false
left: 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate
left: Hydrogen Ion
name: 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate + Hydrogen Ion → Carbon dioxide + Indoleglycerol phosphate + Water
conversion direction: LEFT_TO_RIGHT

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

Indolelactic acid
type: SmallMoleculeReference
xref: Reference/PubChem-compound 92904
xref: Reference/ChemSpider 83867
xref: Reference/KEGG Compound C02043
xref: Reference/ChEBI CHEBI 24813
xref: Reference/HMDB HMDB0000671
xref: Reference/CAS 1821-52-9
chemical formula: C11H11NO3
molecular weight: 205.0739
structure: ChemicalStructure/PW C000528

Reference/PubChem-compound 64689
type: UnificationXref
id: 64689
db: PubChem-compound

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

Reference/ChEBI CHEBI 24813
type: UnificationXref
id: CHEBI:24813
db: ChEBI

Phosphoadenosine phosphosulfate
type: SmallMoleculeReference
xref: Reference/BioCyc PAPS
xref: Reference/HMDB HMDB0001134
xref: Reference/CAS 482-67-7
xref: Reference/ChemSpider 9799
xref: Reference/KEGG Compound C00053
xref: Reference/PubChem-compound 10214
xref: Reference/ChEBI CHEBI 17980
chemical formula: C10H15N5O13P2S
molecular weight: 506.98624
structure: ChemicalStructure/PW C000886

L-Glutamine
type: SmallMolecule
cellular location: Chloroplast
entity reference: L-Glutamine

Reference/ChemSpider 140102
type: UnificationXref
id: 140102
db: ChemSpider

Reference/KEGG Compound C00054
type: UnificationXref
id: C00054
db: KEGG Compound

Reference/KEGG Compound C00053
type: UnificationXref
id: C00053
db: KEGG Compound

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

Reference/CAS 591-59-3
type: UnificationXref
id: 591-59-3
db: CAS

Reference/HMDB HMDB0001123
type: UnificationXref
id: HMDB0001123
db: HMDB

ChemicalStructure/PW C000395
type: ChemicalStructure
structure format: SMILES

Reference/KEGG Compound C16517
type: UnificationXref
id: C16517
db: KEGG Compound

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

Reference/KEGG Compound C16516
type: UnificationXref
id: C16516
db: KEGG Compound

indolylmethyl-desulfoglucosinolate
type: SmallMolecule
entity reference: indolylmethyl-desulfoglucosinolate

ReactionCatalysis7294
type: Catalysis
controller: Anthranilate phosphoribosyltransferase, chloroplastic
controlled: 2.4.2.18
control type: ACTIVATION

Compound/PW C045262 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: indole-3-acetohydroximoyl-glutathione
stoichiometric coefficient: 1.0

Reference/UniProt O65790
type: UnificationXref
id: O65790
db: UniProt

ReactionCatalysis7297
type: Catalysis
controller: Tryptophan synthase beta chain 2, chloroplastic
controlled: Reaction7325
control type: ACTIVATION

ReactionCatalysis7296
type: Catalysis
controller: Tryptophan synthase beta chain 2, chloroplastic
controlled: 4.2.1.20
control type: ACTIVATION

Reference/ChemSpider 65566987
type: UnificationXref
id: 65566987
db: ChemSpider

ReactionCatalysis7295
type: Catalysis
controller: N-(5'-phosphoribosyl)anthranilate isomerase 2, chloroplastic
controlled: 5.3.1.24
control type: ACTIVATION

N-(5-phosphoribosyl)-anthranilate
type: SmallMolecule
entity reference: N-(5-phosphoribosyl)-anthranilate

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

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

Reference/PubChem-compound 10214
type: UnificationXref
id: 10214
db: PubChem-compound

Reference/UniProt Q42527
type: UnificationXref
id: Q42527
db: UniProt

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

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

Reference/HMDB HMDB0001134
type: UnificationXref
id: HMDB0001134
db: HMDB

ChemicalStructure/PW C000043
type: ChemicalStructure
structure format: SMILES

S-Adenosylhomocysteine
type: SmallMolecule
cellular location: Cytosol
entity reference: S-Adenosylhomocysteine

Reference/CAS 5187-84-8
type: UnificationXref
id: 5187-84-8
db: CAS

Reference/UniProt P25269
type: UnificationXref
id: P25269
db: UniProt

Reference/HMDB HMDB0000280
type: UnificationXref
id: HMDB0000280
db: HMDB

Compound/PW C000043 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Adenosine 3',5'-diphosphate
stoichiometric coefficient: 1.0

2-Aminobenzoic acid
type: SmallMolecule
cellular location: Chloroplast
entity reference: 2-Aminobenzoic acid

N-hydroxy-L-tryptophan
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 58728
xref: Reference/PubChem-compound 45266744
chemical formula: C11H11N2O3
molecular weight: 219.07751
structure: ChemicalStructure/PW C045257

Reference/HMDB HMDB0000286
type: UnificationXref
id: HMDB0000286
db: HMDB

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

Reference/ChemSpider 31983
type: UnificationXref
id: 31983
db: ChemSpider

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

indole-3-acetohydroximoyl-glutathione
type: SmallMolecule
cellular location: Cytosol
entity reference: indole-3-acetohydroximoyl-glutathione

Indole
type: SmallMoleculeReference
xref: Reference/ChemSpider 776
xref: Reference/PubChem-compound 798
xref: Reference/BioCyc INDOLE
xref: Reference/CAS 120-72-9
xref: Reference/KEGG Compound C00463
xref: Reference/HMDB HMDB0000738
xref: Reference/ChEBI CHEBI 16881
chemical formula: C8H7N
molecular weight: 117.057846
structure: ChemicalStructure/PW C000587

Reference/KEGG Compound C00078
type: UnificationXref
id: C00078
db: KEGG Compound

Reference/CAS 58-98-0
type: UnificationXref
id: 58-98-0
db: CAS

Reference/PubChem-compound 49859657
type: UnificationXref
id: 49859657
db: PubChem-compound

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

Hydrogen peroxide
type: SmallMolecule
cellular location: Cytosol
entity reference: Hydrogen peroxide

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

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

Reference/PubChem-compound 729
type: UnificationXref
id: 729
db: PubChem-compound

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

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

Reference/HMDB HMDB0000295
type: UnificationXref
id: HMDB0000295
db: HMDB

Reference/ChemSpider 5809
type: UnificationXref
id: 5809
db: ChemSpider

Compound/PW C000395 Peroxisome/Stoichiometry/1.0
type: Stoichiometry
physical entity: β-D-Glucose
stoichiometric coefficient: 1.0

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

β-D-Glucose
type: SmallMolecule
cellular location: Peroxisome
entity reference: β-D-Glucose

Reference/ChEBI CHEBI 18086
type: UnificationXref
id: CHEBI:18086
db: ChEBI

Reference/PubChem-compound 45266744
type: UnificationXref
id: 45266744
db: PubChem-compound

Reference/PubChem-compound 45266745
type: UnificationXref
id: 45266745
db: PubChem-compound

Compound/PW C000877 Chloroplast/Stoichiometry/1.0
type: Stoichiometry
physical entity: 2-Aminobenzoic acid
stoichiometric coefficient: 1.0

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

Reference/HMDB HMDB0000061
type: UnificationXref
id: HMDB0000061
db: HMDB

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

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

Compound/PW C000869/Stoichiometry/1.0
type: Stoichiometry
physical entity: D-Glyceraldehyde 3-phosphate
stoichiometric coefficient: 1.0

Tryptamine
type: SmallMoleculeReference
xref: Reference/CAS 61-54-1
xref: Reference/PubChem-compound 1150
xref: Reference/ChEBI CHEBI 16765
xref: Reference/HMDB HMDB0000303
xref: Reference/ChemSpider 1118
xref: Reference/BioCyc TRYPTAMINE
xref: Reference/KEGG Compound C00398
chemical formula: C10H12N2
molecular weight: 160.10005
structure: ChemicalStructure/PW C000207

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

4-hydroxy-3-indolylmethyl-glucosinolate
type: SmallMolecule
cellular location: Cytosol
entity reference: 4-hydroxy-3-indolylmethyl-glucosinolate

1.2.3.14,1.2.3.7
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040034 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001783 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000926 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001065 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000528 Cytosol/Stoichiometry/1.0
right: Hydrogen Ion
right: Hydrogen peroxide
right: Indolelactic acid
spontaneous: false
EC number: 1.2.3.14,1.2.3.7
left: Oxygen
left: Indoleacetaldehyde
left: Water
name: Indoleacetaldehyde + Oxygen + Water → Hydrogen Ion + Hydrogen peroxide + Indolelactic acid
conversion direction: LEFT_TO_RIGHT

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

Reference/PubChem-compound 25246222
type: UnificationXref
id: 25246222
db: PubChem-compound

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

Reference/KEGG Compound C02043
type: UnificationXref
id: C02043
db: KEGG Compound

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

Glucobrassicin
type: SmallMoleculeReference
xref: Reference/CAS 4356-52-9
xref: Reference/PubChem-compound 9601691
xref: Reference/HMDB HMDB0030243
xref: Reference/ChemSpider 7875815
chemical formula: C16H20N2O9S2
molecular weight: 448.06104
structure: ChemicalStructure/PW C011457

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

Abscisic-aldehyde oxidase
type: Protein
cellular location: Cytosol
entity reference: Abscisic-aldehyde oxidase

ChemicalStructure/PW C000190
type: ChemicalStructure
structure format: SMILES

Ammonium
type: SmallMolecule
cellular location: Cytosol
entity reference: Ammonium

Glucobrassicin
type: SmallMolecule
entity reference: Glucobrassicin

Cytochrome P450 81F3
type: Protein
cellular location: Cytosol
entity reference: Cytochrome P450 81F3

ChemicalStructure/PW C000193
type: ChemicalStructure
structure format: SMILES

Reaction7337
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001783 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001065 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000926 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000207 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C022608 Cytosol/Stoichiometry/1.0
right: Ammonium
right: Hydrogen peroxide
right: Indoleacetaldehyde
spontaneous: false
left: Oxygen
left: Tryptamine
left: Water
name: Oxygen + Tryptamine + Water → Ammonium + Hydrogen peroxide + Indoleacetaldehyde
conversion direction: LEFT_TO_RIGHT

4.1.3.27
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000877 Chloroplast/Stoichiometry/1.0
participant stoichiometry: Compound/PW C007748 Chloroplast/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000095 Chloroplast/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000500 Chloroplast/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000164 Chloroplast/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034 Chloroplast/Stoichiometry/1.0
right: Hydrogen Ion
right: Pyruvic acid
right: 2-Aminobenzoic acid
right: L-Glutamic acid
spontaneous: false
EC number: 4.1.3.27
left: Chorismate
left: L-Glutamine
name: Chorismate + L-Glutamine → 2-Aminobenzoic acid + Hydrogen Ion + L-Glutamic acid + Pyruvic acid
conversion direction: LEFT_TO_RIGHT

Glucobrassicin
type: SmallMolecule
cellular location: Endoplasmic Reticulum
entity reference: Glucobrassicin

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

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

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

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

Carbon dioxide
type: SmallMolecule
entity reference: Carbon dioxide

Indole
type: SmallMolecule
entity reference: Indole

Reference/PubChem-compound 49859627
type: UnificationXref
id: 49859627
db: PubChem-compound

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

Reference/CAS 118-92-3
type: UnificationXref
id: 118-92-3
db: CAS

Phosphoadenosine phosphosulfate
type: SmallMolecule
cellular location: Cytosol
entity reference: Phosphoadenosine phosphosulfate

ChemicalStructure/PW C000080
type: ChemicalStructure
structure format: SMILES

2.4.2.18
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000170/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000877/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000190/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040925/Stoichiometry/1.0
right: N-(5-phosphoribosyl)-anthranilate
right: Pyrophosphate
spontaneous: false
EC number: 2.4.2.18
left: 2-Aminobenzoic acid
left: Phosphoribosyl pyrophosphate
name: 2-Aminobenzoic acid + Phosphoribosyl pyrophosphate → N-(5-phosphoribosyl)-anthranilate + Pyrophosphate
conversion direction: LEFT_TO_RIGHT

Reference/ChEBI CHEBI 15903
type: UnificationXref
id: CHEBI:15903
db: ChEBI

4.2.1.20
type: BiochemicalReaction
participant stoichiometry: Compound/PW C044564/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000587/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000869/Stoichiometry/1.0
right: D-Glyceraldehyde 3-phosphate
right: Indole
spontaneous: false
EC number: 4.2.1.20
left: Indoleglycerol phosphate
name: Indoleglycerol phosphate → D-Glyceraldehyde 3-phosphate + Indole
conversion direction: LEFT_TO_RIGHT

5.3.1.24
type: BiochemicalReaction
participant stoichiometry: Compound/PW C042673/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040925/Stoichiometry/1.0
right: 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate
spontaneous: false
EC number: 5.3.1.24
left: N-(5-phosphoribosyl)-anthranilate
name: N-(5-phosphoribosyl)-anthranilate → 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate
conversion direction: LEFT_TO_RIGHT

Reaction7325
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000741/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000587/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000120/Stoichiometry/1.0
right: Water
right: L-Tryptophan
spontaneous: false
left: L-Serine
left: Indole
name: Indole + L-Serine → L-Tryptophan + Water
conversion direction: LEFT_TO_RIGHT

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

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

Compound/PW C045264 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: indolylmethylthiohydroximate
stoichiometric coefficient: 1.0

Reference/UniProt P32068
type: UnificationXref
id: P32068
db: UniProt

Reference/ChEBI CHEBI 74814
type: UnificationXref
id: CHEBI:74814
db: ChEBI

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

Reference/UniProt P32069
type: UnificationXref
id: P32069
db: UniProt

ChemicalStructure/PW C000207
type: ChemicalStructure
structure format: SMILES
structure data: NCCC1=CNC2=C1C=CC=C2

Compound/PW C000749 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: S-Adenosylhomocysteine
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

Reference/CAS 4356-52-9
type: UnificationXref
id: 4356-52-9
db: CAS

4.4.1.-
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040034 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045263 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045264 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C010294 Cytosol/Stoichiometry/1.0
right: Hydrogen Ion
right: Serylglycine
right: indolylmethylthiohydroximate
spontaneous: false
EC number: 4.4.1.-
left: indole-3-acetohydroximoyl-cysteinylglycine
left: Water
name: Water + indole-3-acetohydroximoyl-cysteinylglycine → Hydrogen Ion + Serylglycine + indolylmethylthiohydroximate
conversion direction: LEFT_TO_RIGHT

ChemicalStructure/PW C011457
type: ChemicalStructure
structure format: SMILES

Reaction7352
type: BiochemicalReaction
participant stoichiometry: Compound/PW C045262 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045263 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000095 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420 Cytosol/Stoichiometry/1.0
right: indole-3-acetohydroximoyl-cysteinylglycine
right: L-Glutamic acid
spontaneous: false
left: indole-3-acetohydroximoyl-glutathione
left: Water
name: Water + indole-3-acetohydroximoyl-glutathione → L-Glutamic acid + indole-3-acetohydroximoyl-cysteinylglycine
conversion direction: LEFT_TO_RIGHT

Reference/ChemSpider 4573686
type: UnificationXref
id: 4573686
db: ChemSpider

2.8.2.-
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040034 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045265 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000043/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045265/Stoichiometry/1.0
participant stoichiometry: Compound/PW C011457/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000043 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C011457 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000886/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000886 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Adenosine 3',5'-diphosphate
right: Hydrogen Ion
right: Glucobrassicin
spontaneous: false
EC number: 2.8.2.-
left: Phosphoadenosine phosphosulfate
left: indolylmethyl-desulfoglucosinolate
name: Phosphoadenosine phosphosulfate + indolylmethyl-desulfoglucosinolate → Adenosine 3',5'-diphosphate + Glucobrassicin + Hydrogen Ion
conversion direction: LEFT_TO_RIGHT

2.4.1.-,2.4.1.195
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000193 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045264 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045265 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000201 Cytosol/Stoichiometry/1.0
right: Uridine 5'-diphosphate
right: indolylmethyl-desulfoglucosinolate
spontaneous: false
EC number: 2.4.1.-,2.4.1.195
left: Uridine diphosphate glucose
left: indolylmethylthiohydroximate
name: Uridine diphosphate glucose + indolylmethylthiohydroximate → Uridine 5'-diphosphate + indolylmethyl-desulfoglucosinolate
conversion direction: LEFT_TO_RIGHT

Pyrophosphate
type: SmallMolecule
entity reference: Pyrophosphate

β-D-Glucose
type: SmallMoleculeReference
xref: Reference/PubChem-compound 64689
xref: Reference/ChemSpider 58238
xref: Reference/HMDB HMDB0000516
xref: Reference/KEGG Compound C00221
xref: Reference/CAS 492-61-5
xref: Reference/ChEBI CHEBI 15903
chemical formula: C6H12O6
molecular weight: 180.06339
structure: ChemicalStructure/PW C000395

1.14.-.-
type: BiochemicalReaction
participant stoichiometry: Compound/PW C019230 Endoplasmic Reticulum/Stoichiometry/1.0
participant stoichiometry: Compound/PW C011457 Endoplasmic Reticulum/Stoichiometry/1.0
right: Neoglucobrassicin
spontaneous: false
EC number: 1.14.-.-
left: Glucobrassicin
name: Glucobrassicin → Neoglucobrassicin
conversion direction: LEFT_TO_RIGHT

3.2.1.21
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000395 Peroxisome/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420 Peroxisome/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045266 Peroxisome/Stoichiometry/1.0
participant stoichiometry: Compound/PW C011457 Peroxisome/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034 Peroxisome/Stoichiometry/1.0
right: indolylmethyl glucosinolate aglycone
right: Hydrogen Ion
right: β-D-Glucose
spontaneous: false
EC number: 3.2.1.21
left: Water
left: Glucobrassicin
name: Glucobrassicin + Water → Hydrogen Ion + indolylmethyl glucosinolate aglycone + β-D-Glucose
conversion direction: LEFT_TO_RIGHT

indolylmethylthiohydroximate
type: SmallMolecule
cellular location: Cytosol
entity reference: indolylmethylthiohydroximate

2.1.1.-
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000749 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000921 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045267 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045268 Cytosol/Stoichiometry/1.0
right: S-Adenosylhomocysteine
right: 4-methoxy-3-indolylmethyl-glucosinolate
right: Hydrogen Ion
spontaneous: false
EC number: 2.1.1.-
left: 4-hydroxy-3-indolylmethyl-glucosinolate
left: S-Adenosylmethionine
name: 4-hydroxy-3-indolylmethyl-glucosinolate + S-Adenosylmethionine → 4-methoxy-3-indolylmethyl-glucosinolate + Hydrogen Ion + S-Adenosylhomocysteine
conversion direction: LEFT_TO_RIGHT

1.14.-.-
type: BiochemicalReaction
participant stoichiometry: Compound/PW C011457 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045267 Cytosol/Stoichiometry/1.0
right: 4-hydroxy-3-indolylmethyl-glucosinolate
spontaneous: false
EC number: 1.14.-.-
left: Glucobrassicin
name: Glucobrassicin → 4-hydroxy-3-indolylmethyl-glucosinolate
conversion direction: LEFT_TO_RIGHT

Hydrogen Ion
type: SmallMolecule
cellular location: Chloroplast
entity reference: Hydrogen Ion

Reference/CAS 120-72-9
type: UnificationXref
id: 120-72-9
db: CAS

Indole glucosinolate O-methyltransferase 1
type: Protein
cellular location: Cytosol
entity reference: Indole glucosinolate O-methyltransferase 1

Reaction7351
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000080 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045262 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045261 Cytosol/Stoichiometry/1.0
right: Glutathione
right: indole-3-acetohydroximoyl-glutathione
spontaneous: false
left: indole-3-acetonitrile oxide
name: indole-3-acetonitrile oxide → Glutathione + indole-3-acetohydroximoyl-glutathione
conversion direction: LEFT_TO_RIGHT

1.14.-.-
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040034 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000146 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000143 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045261 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045260 Cytosol/Stoichiometry/1.0
right: Hydrogen Ion
right: indole-3-acetonitrile oxide
right: NADPH
spontaneous: false
EC number: 1.14.-.-
left: (Z)-indol-3-ylacetaldoxime
left: NADP
name: (Z)-indol-3-ylacetaldoxime + NADP → Hydrogen Ion + NADPH + indole-3-acetonitrile oxide
conversion direction: LEFT_TO_RIGHT

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

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

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

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

Reaction7349
type: BiochemicalReaction
participant stoichiometry: Compound/PW C045259 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045260 Cytosol/Stoichiometry/1.0
right: (Z)-indol-3-ylacetaldoxime
spontaneous: true
left: (E)-indol-3-ylacetaldoxime
name: (E)-indol-3-ylacetaldoxime → (Z)-indol-3-ylacetaldoxime
conversion direction: LEFT_TO_RIGHT

ChemicalStructure/PW C000587
type: ChemicalStructure
structure format: SMILES
structure data: N1C=CC2=C1C=CC=C2

Reference/HMDB HMDB0000303
type: UnificationXref
id: HMDB0000303
db: HMDB

Adenosine 3',5'-diphosphate
type: SmallMolecule
entity reference: Adenosine 3',5'-diphosphate

ChemicalStructure/PW C045258
type: ChemicalStructure
structure format: SMILES
structure data: ON(O)C(CC1=CNC2=C1C=CC=C2)C([O-])=O

ChemicalStructure/PW C045257
type: ChemicalStructure
structure format: SMILES
structure data: [H][C@@](CC1=CNC2=CC=CC=C12)(NO)C([O-])=O

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

Adenosine 3',5'-diphosphate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 17985
xref: Reference/CAS 1053-73-2
xref: Reference/PubChem-compound 159296
xref: Reference/ChemSpider 140102
xref: Reference/BioCyc 3-5-ADP
xref: Reference/KEGG Compound C00054
xref: Reference/HMDB HMDB0000061
chemical formula: C10H15N5O10P2
molecular weight: 427.02942
structure: ChemicalStructure/PW C000043

Reaction7345
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000741 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000146 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001065 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000143 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045257 Cytosol/Stoichiometry/1.0
right: N-hydroxy-L-tryptophan
right: NADP
right: Water
spontaneous: false
left: Oxygen
left: L-Tryptophan
left: NADPH
name: L-Tryptophan + NADPH + Oxygen → N-hydroxy-L-tryptophan + NADP + Water
conversion direction: LEFT_TO_RIGHT

Compound/PW C045257 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: N-hydroxy-L-tryptophan
stoichiometric coefficient: 1.0

Reaction7348
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040034 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001316 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045259 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045258 Cytosol/Stoichiometry/1.0
right: Carbon dioxide
right: (E)-indol-3-ylacetaldoxime
right: Water
spontaneous: false
left: Hydrogen Ion
left: N,N-dihydroxy-L-tryptophan
name: Hydrogen Ion + N,N-dihydroxy-L-tryptophan → (E)-indol-3-ylacetaldoxime + Carbon dioxide + Water
conversion direction: LEFT_TO_RIGHT

Reaction7347
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040034 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000146 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001065 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000143 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045257 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C045258 Cytosol/Stoichiometry/1.0
right: N,N-dihydroxy-L-tryptophan
right: NADP
right: Water
spontaneous: false
left: Oxygen
left: N-hydroxy-L-tryptophan
left: Hydrogen Ion
left: NADPH
name: Hydrogen Ion + N-hydroxy-L-tryptophan + NADPH + Oxygen → N,N-dihydroxy-L-tryptophan + NADP + Water
conversion direction: LEFT_TO_RIGHT

Reference/PubChem-compound 1150
type: UnificationXref
id: 1150
db: PubChem-compound

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

ChemicalStructure/PW C045259
type: ChemicalStructure
structure format: SMILES
structure data: [H]\C(CC1=CNC2=CC=CC=C12)=N/O

ChemicalStructure/PW C040925
type: ChemicalStructure
structure format: SMILES
structure data: OC1C(O)C(NC2=C(C=CC=C2)C([O-])=O)OC1COP([O-])([O-])=O

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

indole-3-acetonitrile oxide
type: SmallMolecule
cellular location: Cytosol
entity reference: indole-3-acetonitrile oxide

Serylglycine
type: SmallMoleculeReference
xref: Reference/PubChem-compound 7009644
xref: Reference/ChEBI CHEBI 74814
xref: Reference/ChemSpider 65566987
xref: Reference/BioCyc CPD-12607
xref: Reference/CAS 687-63-8
xref: Reference/HMDB HMDB0029039
chemical formula: C5H10N2O4
molecular weight: 162.06406
structure: ChemicalStructure/PW C010294

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

ChemicalStructure/PW C045261
type: ChemicalStructure
structure format: SMILES
structure data: [O-][N+]#CCC1=CNC2=CC=CC=C12

ChemicalStructure/PW C045260
type: ChemicalStructure
structure format: SMILES
structure data: [H]\C(CC1=CNC2=CC=CC=C12)=N\O

Reference/PubChem-compound 46173098
type: UnificationXref
id: 46173098
db: PubChem-compound

Reference/ChEBI CHEBI 62725
type: UnificationXref
id: CHEBI:62725
db: ChEBI

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

ChemicalStructure/PW C045267
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C045266
type: ChemicalStructure
structure format: SMILES
structure data: [O-]S(=O)(=O)ON=C([S-])CC1=CNC2=CC=CC=C12

ChemicalStructure/PW C045268
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C045263
type: ChemicalStructure
structure format: SMILES
structure data: NC(CS\C(CC1=CNC2=CC=CC=C12)=N/O)C(O)=NCC(O)=O

ChemicalStructure/PW C045262
type: ChemicalStructure
structure format: SMILES
structure data: NC(CCC([O-])=NC(CS\C(CC1=CNC2=CC=CC=C12)=N/O)C(O)=NCC(O)=O)C(O)=O

Reference/HMDB HMDB0000671
type: UnificationXref
id: HMDB0000671
db: HMDB

ChemicalStructure/PW C045265
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C045264
type: ChemicalStructure
structure format: SMILES
structure data: [O-]N=C(S)CC1=C[NH2+]C2=CC=CC=C12

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

Compound/PW C000877/Stoichiometry/1.0
type: Stoichiometry
physical entity: 2-Aminobenzoic acid
stoichiometric coefficient: 1.0

Reference/CAS 485-80-3
type: UnificationXref
id: 485-80-3
db: CAS

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

ChemicalStructure/PW C000201
type: ChemicalStructure
structure format: SMILES

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

Reference/BioCyc 3-5-ADP
type: UnificationXref
id: 3-5-ADP
db: BioCyc

Reference/PubChem-compound 25245040
type: UnificationXref
id: 25245040
db: PubChem-compound

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

Glucobrassicin
type: SmallMolecule
cellular location: Cytosol
entity reference: Glucobrassicin

ChemicalStructure/PW C010294
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CO)C(=O)NCC(O)=O

Adenosine 3',5'-diphosphate
type: SmallMolecule
cellular location: Cytosol
entity reference: Adenosine 3',5'-diphosphate

UDP-glycosyltransferase 74B1
type: Protein
cellular location: Cytosol
entity reference: UDP-glycosyltransferase 74B1

Beta-glucosidase 26, peroxisomal
type: Protein
cellular location: Peroxisome
entity reference: Beta-glucosidase 26, peroxisomal

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

N,N-dihydroxy-L-tryptophan
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 58729
xref: Reference/PubChem-compound 45266745
chemical formula: C11H11N2O4
molecular weight: 235.07243
structure: ChemicalStructure/PW C045258

(E)-indol-3-ylacetaldoxime
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 17545
xref: Reference/KEGG Compound C02937
xref: Reference/ChemSpider 4522197
xref: Reference/PubChem-compound 5371769
chemical formula: C10H10N2O
molecular weight: 174.07932
structure: ChemicalStructure/PW C045259

Reference/CAS 1053-73-2
type: UnificationXref
id: 1053-73-2
db: CAS

Anthranilate synthase alpha subunit 2, chloroplastic
type: Protein
cellular location: Chloroplast
entity reference: Anthranilate synthase alpha subunit 2, chloroplastic

Reference/ChEBI CHEBI 16856
type: UnificationXref
id: CHEBI:16856
db: ChEBI

Compound/PW C045265/Stoichiometry/1.0
type: Stoichiometry
physical entity: indolylmethyl-desulfoglucosinolate
stoichiometric coefficient: 1.0

Reference/ChEBI CHEBI 27506
type: UnificationXref
id: CHEBI:27506
db: ChEBI

Carbon dioxide
type: SmallMolecule
cellular location: Cytosol
entity reference: Carbon dioxide

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

N-(5-phosphoribosyl)-anthranilate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 18277
chemical formula: C12H13NO9P
molecular weight: 346.03442
structure: ChemicalStructure/PW C040925

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

Uridine diphosphate glucose
type: SmallMoleculeReference
xref: Reference/BioCyc UDP-GLUCOSE
xref: Reference/KEGG Compound C00029
xref: Reference/PubChem-compound 53477679
xref: Reference/CAS 133-89-1
xref: Reference/HMDB HMDB0000286
chemical formula: C15H24N2O17P2
molecular weight: 566.055
structure: ChemicalStructure/PW C000193

Reference/BioCyc UDP-GLUCOSE
type: UnificationXref
id: UDP-GLUCOSE
db: BioCyc

Compound/PW C000741 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Tryptophan
stoichiometric coefficient: 1.0

Phosphoribosyl pyrophosphate
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00119
xref: Reference/ChemSpider 7062
xref: Reference/CAS 7540-64-9
xref: Reference/HMDB HMDB0000280
xref: Reference/PubChem-compound 7339
xref: Reference/BioCyc PRPP
xref: Reference/ChEBI CHEBI 17111
chemical formula: C5H13O14P3
molecular weight: 389.9518
structure: ChemicalStructure/PW C000190

Compound/PW C045263 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: indole-3-acetohydroximoyl-cysteinylglycine
stoichiometric coefficient: 1.0

(Z)-indol-3-ylacetaldoxime
type: SmallMoleculeReference
xref: Reference/PubChem-compound 5459978
xref: Reference/ChemSpider 4573686
xref: Reference/ChEBI CHEBI 48577
chemical formula: C10H10N2O
molecular weight: 174.07932
structure: ChemicalStructure/PW C045260

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

indole-3-acetohydroximoyl-cysteinylglycine
type: SmallMoleculeReference
xref: Reference/PubChem-compound 46173098
chemical formula: C15H18N4O4S
molecular weight: 350.1049
structure: ChemicalStructure/PW C045263

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

indolylmethylthiohydroximate
type: SmallMoleculeReference
xref: Reference/PubChem-compound 25200900
xref: Reference/KEGG Compound C16516
chemical formula: C10H10N2OS
molecular weight: 206.05139
structure: ChemicalStructure/PW C045264

indole-3-acetonitrile oxide
type: SmallMoleculeReference
xref: Reference/PubChem-compound 14524362
chemical formula: C10H8N2O
molecular weight: 172.06366
structure: ChemicalStructure/PW C045261

indole-3-acetohydroximoyl-glutathione
type: SmallMoleculeReference
xref: Reference/PubChem-compound 46173372
chemical formula: C20H24N5O7S
molecular weight: 478.1402
structure: ChemicalStructure/PW C045262

4-hydroxy-3-indolylmethyl-glucosinolate
type: SmallMoleculeReference
xref: Reference/KEGG Compound C08422
xref: Reference/PubChem-compound 49859657
xref: Reference/ChEBI CHEBI 1865
chemical formula: C16H19N2O10S2
molecular weight: 463.04868
structure: ChemicalStructure/PW C045267

4-methoxy-3-indolylmethyl-glucosinolate
type: SmallMoleculeReference
xref: Reference/KEGG Compound C08423
xref: Reference/ChEBI CHEBI 62725
xref: Reference/PubChem-compound 49859627
chemical formula: C17H21N2O10S2
molecular weight: 477.0643
structure: ChemicalStructure/PW C045268

indolylmethyl-desulfoglucosinolate
type: SmallMoleculeReference
xref: Reference/KEGG Compound C16517
xref: Reference/PubChem-compound 14122903
chemical formula: C16H20N2O6S
molecular weight: 368.10422
structure: ChemicalStructure/PW C045265

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

indolylmethyl glucosinolate aglycone
type: SmallMoleculeReference
xref: Reference/PubChem-compound 25245040
chemical formula: C10H8N2O4S2
molecular weight: 283.99365
structure: ChemicalStructure/PW C045266

Reference/PubChem-compound 798
type: UnificationXref
id: 798
db: PubChem-compound

Reference/ChEBI CHEBI 15414
type: UnificationXref
id: CHEBI:15414
db: ChEBI

Reference/PubChem-compound 46878464
type: UnificationXref
id: 46878464
db: PubChem-compound

Reference/ChemSpider 9799
type: UnificationXref
id: 9799
db: ChemSpider

ChemicalStructure/PW C000143
type: ChemicalStructure
structure format: SMILES

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

Reference/UniProt Q02166
type: UnificationXref
id: Q02166
db: UniProt

Glutathione
type: SmallMoleculeReference
xref: Reference/CAS 70-18-8
xref: Reference/HMDB HMDB0000125
xref: Reference/BioCyc OXIDIZED-GLUTATHIONE
xref: Reference/KEGG Compound C00051
xref: Reference/ChEBI CHEBI 16856
xref: Reference/PubChem-compound 124886
xref: Reference/ChemSpider 111188
chemical formula: C10H17N3O6S
molecular weight: 307.0838
structure: ChemicalStructure/PW C000080

Compound/PW C045265 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: indolylmethyl-desulfoglucosinolate
stoichiometric coefficient: 1.0

Cytosolic sulfotransferase 18
type: Protein
cellular location: Cytosol
entity reference: Cytosolic sulfotransferase 18

ChemicalStructure/PW C000146
type: ChemicalStructure
structure format: SMILES

Reference/PubChem-compound 159296
type: UnificationXref
id: 159296
db: PubChem-compound

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

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

Reference/CAS 2591-98-2
type: UnificationXref
id: 2591-98-2
db: CAS

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

Reference/BioCyc INDOLE ACETALDEHYDE
type: UnificationXref
id: INDOLE_ACETALDEHYDE
db: BioCyc

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

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

Reference/PubChem-compound 227
type: UnificationXref
id: 227
db: PubChem-compound

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

Reference/BioCyc S-ADENOSYLMETHIONINE
type: UnificationXref
id: S-ADENOSYLMETHIONINE
db: BioCyc

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

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

Compound/PW C045258 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: N,N-dihydroxy-L-tryptophan
stoichiometric coefficient: 1.0

Anthranilate synthase alpha subunit 1, chloroplastic
type: Protein
cellular location: Chloroplast
entity reference: Anthranilate synthase alpha subunit 1, chloroplastic

Reference/KEGG Compound C08423
type: UnificationXref
id: C08423
db: KEGG Compound

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

Reference/KEGG Compound C08422
type: UnificationXref
id: C08422
db: KEGG Compound

Compound/PW C000043/Stoichiometry/1.0
type: Stoichiometry
physical entity: Adenosine 3',5'-diphosphate
stoichiometric coefficient: 1.0

Anthranilate synthase
type: Complex
cellular location: Chloroplast
component: Anthranilate synthase alpha subunit 1, chloroplastic
component: Anthranilate synthase alpha subunit 2, chloroplastic
component: Anthranilate synthase beta subunit 2, chloroplastic

Compound/PW C000587/Stoichiometry/1.0
type: Stoichiometry
physical entity: Indole
stoichiometric coefficient: 1.0

Reference/ChEBI CHEBI 16828
type: UnificationXref
id: CHEBI:16828
db: ChEBI

Phosphoribosyl pyrophosphate
type: SmallMolecule
entity reference: Phosphoribosyl pyrophosphate

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

Compound/PW C000080 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Glutathione
stoichiometric coefficient: 1.0

Reference/UniProt Q9FJM5
type: UnificationXref
id: Q9FJM5
db: UniProt

Chorismate
type: SmallMolecule
cellular location: Chloroplast
entity reference: Chorismate

(E)-indol-3-ylacetaldoxime
type: SmallMolecule
cellular location: Cytosol
entity reference: (E)-indol-3-ylacetaldoxime

Reference/ChemSpider 6066
type: UnificationXref
id: 6066
db: ChemSpider

Reference/KEGG Compound C08424
type: UnificationXref
id: C08424
db: KEGG Compound

Tryptophan Metabolism
type: Pathway
pathway order: PathwayEnzymeReaction/27224
pathway order: PathwayEnzymeReaction/27223
pathway order: PathwayEnzymeReaction/27226
pathway order: PathwayEnzymeReaction/27567
pathway order: PathwayEnzymeReaction/27225
pathway order: PathwayEnzymeReaction/27569
pathway order: PathwayEnzymeReaction/27800
pathway order: PathwayEnzymeReaction/27227
pathway order: PathwayEnzymeReaction/27568
pathway order: PathwayEnzymeReaction/27240
pathway order: PathwayEnzymeReaction/27241
pathway order: PathwayEnzymeReaction/27576
pathway order: PathwayEnzymeReaction/27796
pathway order: PathwayEnzymeReaction/27795
pathway order: PathwayEnzymeReaction/27798
pathway order: PathwayEnzymeReaction/27239
pathway order: PathwayEnzymeReaction/27238
pathway order: PathwayEnzymeReaction/27799
pathway order: PathwayEnzymeReaction/27251
pathway order: PathwayEnzymeReaction/2123551
pathway order: PathwayEnzymeReaction/27572
pathway order: PathwayEnzymeReaction/27571
pathway order: PathwayEnzymeReaction/27574
pathway order: PathwayEnzymeReaction/27794
pathway order: PathwayEnzymeReaction/27573
pathway order: PathwayEnzymeReaction/27793
pathway component: ReactionCatalysis7320
pathway component: 1.2.3.14,1.2.3.7
pathway component: ReactionCatalysis7309
pathway component: ReactionCatalysis7308
pathway component: 4.4.1.-
pathway component: ReactionCatalysis7324
pathway component: Reaction7352
pathway component: ReactionCatalysis7323
pathway component: 2.8.2.-
pathway component: ReactionCatalysis7322
pathway component: 2.4.1.-,2.4.1.195
pathway component: ReactionCatalysis7321
pathway component: 1.14.-.-
pathway component: 3.2.1.21
pathway component: ReactionCatalysis7327
pathway component: Reaction7337
pathway component: ReactionCatalysis7326
pathway component: 2.1.1.-
pathway component: 4.1.3.27
pathway component: ReactionCatalysis7325
pathway component: ReactionCatalysis7294
pathway component: ReactionCatalysis7297
pathway component: ReactionCatalysis7296
pathway component: Reaction7351
pathway component: ReactionCatalysis7295
pathway component: Reaction7349
pathway component: ReactionCatalysis7319
pathway component: ReactionCatalysis7318
pathway component: ReactionCatalysis7313
pathway component: 2.4.2.18
pathway component: Reaction6530
pathway component: 4.2.1.20
pathway component: Reaction221
pathway component: ReactionCatalysis7317
pathway component: 5.3.1.24
pathway component: Reaction7345
pathway component: ReactionCatalysis7316
pathway component: ReactionCatalysis7315
pathway component: Reaction7348
pathway component: Reaction7325
pathway component: Reaction7347
xref: Reference/PathWhiz PW002556
xref: Reference/SMPDB SMP0002445
organism: Arabidopsis thaliana

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

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

Reference/HMDB HMDB0000125
type: UnificationXref
id: HMDB0000125
db: HMDB

Reference/ChemSpider 222
type: UnificationXref
id: 222
db: ChemSpider

Tryptophan N-monooxygenase 2
type: Protein
cellular location: Cytosol
entity reference: Tryptophan N-monooxygenase 2

Reference/CAS 70-18-8
type: UnificationXref
id: 70-18-8
db: CAS

Reference/ChEBI CHEBI 17985
type: UnificationXref
id: CHEBI:17985
db: ChEBI

Endoplasmic Reticulum
type: CellularLocationVocabulary
xref: Reference/GENE ONTOLOGY GO 0005783

(Z)-indol-3-ylacetaldoxime
type: SmallMolecule
cellular location: Cytosol
entity reference: (Z)-indol-3-ylacetaldoxime

Reference/PubChem-compound 6305
type: UnificationXref
id: 6305
db: PubChem-compound

Reference/HMDB HMDB0000929
type: UnificationXref
id: HMDB0000929
db: HMDB

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

Reference/ChEBI CHEBI 17980
type: UnificationXref
id: CHEBI:17980
db: ChEBI

Compound/PW C011457 Peroxisome/Stoichiometry/1.0
type: Stoichiometry
physical entity: Glucobrassicin
stoichiometric coefficient: 1.0

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

Indole glucosinolate O-methyltransferase
type: Complex
cellular location: Cytosol
component: Indole glucosinolate O-methyltransferase 1
component: Indole glucosinolate O-methyltransferase 2

Reference/PubChem-compound 14122903
type: UnificationXref
id: 14122903
db: PubChem-compound

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

Anthranilate phosphoribosyltransferase, chloroplastic
type: ProteinReference
xref: Reference/UniProt Q02166

Tryptophan synthase beta chain 2, chloroplastic
type: ProteinReference
xref: Reference/UniProt P25269

N-(5'-phosphoribosyl)anthranilate isomerase 2, chloroplastic
type: ProteinReference
xref: Reference/UniProt Q42527

Compound/PW C000926 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Indoleacetaldehyde
stoichiometric coefficient: 1.0

Chorismate
type: SmallMoleculeReference
xref: Reference/CAS 617-12-9
xref: Reference/BioCyc CPD-9517
xref: Reference/KEGG Compound C00251
xref: Reference/PubChem-compound 12039
xref: Reference/ChEBI CHEBI 17333
xref: Reference/ChemSpider 11542
xref: Reference/HMDB HMDB0012199
chemical formula: C10H10O6
molecular weight: 226.04774
structure: ChemicalStructure/PW C007748

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

S-Adenosylmethionine
type: SmallMolecule
cellular location: Cytosol
entity reference: S-Adenosylmethionine

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

Reference/CAS 1821-52-9
type: UnificationXref
id: 1821-52-9
db: CAS

ChemicalStructure/PW C019230
type: ChemicalStructure
structure format: SMILES
structure data: CON1C=C(C\C(SC2OC(CO)C(O)C(O)C2O)=N/OS(O)(=O)=O)C2=CC=CC=C12

Reference/HMDB HMDB0000939
type: UnificationXref
id: HMDB0000939
db: HMDB

ChemicalStructure/PW C000741
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O

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

ChemicalStructure/PW C044564
type: ChemicalStructure
structure format: SMILES
structure data: [H][C@@](O)(COP([O-])([O-])=O)[C@@]([H])(O)C1=CNC2=CC=CC=C12

Anthranilate synthase alpha subunit 1, chloroplastic
type: ProteinReference
xref: Reference/UniProt P32068
organism: Arabidopsis thaliana

Reference/ChemSpider 11542
type: UnificationXref
id: 11542
db: ChemSpider

Cytochrome P450 83B1
type: ProteinReference
xref: Reference/UniProt O65782
organism: Arabidopsis thaliana

Tryptophan N-monooxygenase 2
type: ProteinReference
xref: Reference/UniProt Q501D8
organism: Arabidopsis thaliana

UDP-glycosyltransferase 74B1
type: ProteinReference
xref: Reference/UniProt O48676
organism: Arabidopsis thaliana

S-alkyl-thiohydroximate lyase SUR1
type: ProteinReference
xref: Reference/UniProt Q9SIV0
organism: Arabidopsis thaliana

1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate
type: SmallMolecule
entity reference: 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate

Abscisic-aldehyde oxidase
type: ProteinReference
xref: Reference/UniProt Q7G9P4
organism: Arabidopsis thaliana

Tryptophan N-monooxygenase 1
type: ProteinReference
xref: Reference/UniProt O81346
organism: Arabidopsis thaliana

Reference/HMDB HMDB0030243
type: UnificationXref
id: HMDB0030243
db: HMDB

Anthranilate synthase beta subunit 2, chloroplastic
type: ProteinReference
xref: Reference/UniProt Q9FJM5
organism: Arabidopsis thaliana

Reference/ChemSpider 7875815
type: UnificationXref
id: 7875815
db: ChemSpider

Arabidopsis thaliana
type: BioSource
xref: Reference/TAXONOMY 3702

Anthranilate synthase alpha subunit 2, chloroplastic
type: ProteinReference
xref: Reference/UniProt P32069
organism: Arabidopsis thaliana

Reference/CAS 617-12-9
type: UnificationXref
id: 617-12-9
db: CAS

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

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

Reference/PubChem-compound 46173372
type: UnificationXref
id: 46173372
db: PubChem-compound

Reference/SMPDB SMP0002445
type: UnificationXref
id: SMP0002445
db: SMPDB

indolylmethyl-desulfoglucosinolate
type: SmallMolecule
cellular location: Cytosol
entity reference: indolylmethyl-desulfoglucosinolate

Reference/GENE ONTOLOGY GO 0005783
type: UnificationXref
id: GO:0005783
db: GENE ONTOLOGY

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

Water
type: SmallMolecule
cellular location: Cytosol
entity reference: Water

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

Reference/UniProt O48676
type: UnificationXref
id: O48676
db: UniProt

Indole glucosinolate O-methyltransferase 2
type: ProteinReference
xref: Reference/UniProt Q9LPU7
organism: Arabidopsis thaliana

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

Cytochrome P450 81F1
type: Protein
cellular location: Cytosol
entity reference: Cytochrome P450 81F1

Indole glucosinolate O-methyltransferase 1
type: ProteinReference
xref: Reference/UniProt Q9LPU5
organism: Arabidopsis thaliana

Reference/ChEBI CHEBI 16765
type: UnificationXref
id: CHEBI:16765
db: ChEBI

Cytochrome P450 81F3
type: ProteinReference
xref: Reference/UniProt Q0WTF4
organism: Arabidopsis thaliana

N-hydroxy-L-tryptophan
type: SmallMolecule
cellular location: Cytosol
entity reference: N-hydroxy-L-tryptophan

Cytochrome P450 81F4
type: ProteinReference
xref: Reference/UniProt Q9SZU1
organism: Arabidopsis thaliana

Cytochrome P450 81F1
type: ProteinReference
xref: Reference/UniProt O65790
organism: Arabidopsis thaliana

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

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

Cytochrome P450 81F2
type: ProteinReference
xref: Reference/UniProt Q9LVD6
organism: Arabidopsis thaliana

Cytosolic sulfotransferase 18
type: ProteinReference
xref: Reference/UniProt Q9C9C9
organism: Arabidopsis thaliana

Beta-glucosidase 26, peroxisomal
type: ProteinReference
xref: Reference/UniProt O64883
organism: Arabidopsis thaliana

Cytosolic sulfotransferase 16
type: ProteinReference
xref: Reference/UniProt Q9C9D0

Compound/PW C040925/Stoichiometry/1.0
type: Stoichiometry
physical entity: N-(5-phosphoribosyl)-anthranilate
stoichiometric coefficient: 1.0

Reference/ChEBI CHEBI 16881
type: UnificationXref
id: CHEBI:16881
db: ChEBI

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

Reference/PubChem-compound 5371769
type: UnificationXref
id: 5371769
db: PubChem-compound

Reference/GENE ONTOLOGY GO 0005777
type: UnificationXref
id: GO:0005777
db: GENE ONTOLOGY

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

Reference/UniProt O81346
type: UnificationXref
id: O81346
db: UniProt

Reference/ChEBI CHEBI 17545
type: UnificationXref
id: CHEBI:17545
db: ChEBI

Reference/BioCyc CPD-9517
type: UnificationXref
id: CPD-9517
db: BioCyc

Reference/KEGG Compound C02937
type: UnificationXref
id: C02937
db: KEGG Compound

Reference/UniProt Q501D8
type: UnificationXref
id: Q501D8
db: UniProt

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

Reference/KEGG Compound C00637
type: UnificationXref
id: C00637
db: KEGG Compound

Uridine diphosphate glucose
type: SmallMolecule
cellular location: Cytosol
entity reference: Uridine diphosphate glucose

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

ChemicalStructure/PW C000886
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C000528
type: ChemicalStructure
structure format: SMILES
structure data: O[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O

Reference/ChEBI CHEBI 30754
type: UnificationXref
id: CHEBI:30754
db: ChEBI

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

Compound/PW C042673/Stoichiometry/1.0
type: Stoichiometry
physical entity: 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate
stoichiometric coefficient: 1.0

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

Reference/ChEBI CHEBI 48577
type: UnificationXref
id: CHEBI:48577
db: ChEBI

Reference/HMDB HMDB0029039
type: UnificationXref
id: HMDB0029039
db: HMDB

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

Reference/PathWhiz PW002556
type: UnificationXref
id: PW002556
db: PathWhiz

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

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

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

Chloroplast
type: CellularLocationVocabulary
xref: Reference/GENE ONTOLOGY GO 0009507

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

Reference/HMDB HMDB0000738
type: UnificationXref
id: HMDB0000738
db: HMDB

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

Compound/PW C011457 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Glucobrassicin
stoichiometric coefficient: 1.0

Oxygen
type: SmallMolecule
cellular location: Cytosol
entity reference: Oxygen

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

Tryptophan N-monooxygenase 1
type: Protein
cellular location: Cytosol
entity reference: Tryptophan N-monooxygenase 1

Reference/PubChem-compound 25200900
type: UnificationXref
id: 25200900
db: PubChem-compound

Reference/ChemSpider 111188
type: UnificationXref
id: 111188
db: ChemSpider

Anthranilate synthase beta subunit 2, chloroplastic
type: Protein
cellular location: Chloroplast
entity reference: Anthranilate synthase beta subunit 2, chloroplastic

Reference/ChemSpider 4522197
type: UnificationXref
id: 4522197
db: ChemSpider

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

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

ChemicalStructure/PW C000749
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C000869
type: ChemicalStructure
structure format: SMILES
structure data: OC(COP(O)(O)=O)C=O

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

Tryptamine
type: SmallMolecule
cellular location: Cytosol
entity reference: Tryptamine

Reference/UniProt Q0WTF4
type: UnificationXref
id: Q0WTF4
db: UniProt

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

Reference/BioCyc CPD-12607
type: UnificationXref
id: CPD-12607
db: BioCyc

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

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

Reference/ChEBI CHEBI 17659
type: UnificationXref
id: CHEBI:17659
db: ChEBI

Serylglycine
type: SmallMolecule
cellular location: Cytosol
entity reference: Serylglycine

Compound/PW C019230 Endoplasmic Reticulum/Stoichiometry/1.0
type: Stoichiometry
physical entity: Neoglucobrassicin
stoichiometric coefficient: 1.0

ChemicalStructure/PW C000877
type: ChemicalStructure
structure format: SMILES
structure data: NC1=CC=CC=C1C(O)=O

Reference/KEGG Compound C00661
type: UnificationXref
id: C00661
db: KEGG Compound

Reference/HMDB HMDB0000516
type: UnificationXref
id: HMDB0000516
db: HMDB

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

Reference/ChEBI CHEBI 16680
type: UnificationXref
id: CHEBI:16680
db: ChEBI

Reference/PubChem-compound 12039
type: UnificationXref
id: 12039
db: PubChem-compound

Reference/PubChem-compound 24762165
type: UnificationXref
id: 24762165
db: PubChem-compound

Reference/HMDB HMDB0000641
type: UnificationXref
id: HMDB0000641
db: HMDB

Reaction221
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000741 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001316 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000207 Cytosol/Stoichiometry/1.0
right: Tryptamine
right: Carbon dioxide
spontaneous: false
left: L-Tryptophan
name: L-Tryptophan ? Carbon dioxide + Tryptamine

Compound/PW C000886/Stoichiometry/1.0
type: Stoichiometry
physical entity: Phosphoadenosine phosphosulfate
stoichiometric coefficient: 1.0

Compound/PW C011457 Endoplasmic Reticulum/Stoichiometry/1.0
type: Stoichiometry
physical entity: Glucobrassicin
stoichiometric coefficient: 1.0

Compound/PW C000886 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: Phosphoadenosine phosphosulfate
stoichiometric coefficient: 1.0