Reference/ChEBI CHEBI 50608
type: UnificationXref
id: CHEBI:50608
db: ChEBI

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

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

Reference/ChEBI CHEBI 50606
type: UnificationXref
id: CHEBI:50606
db: ChEBI

2.7.1.26
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000414/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000165/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001170/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Adenosine diphosphate
right: Hydrogen Ion
right: Flavin Mononucleotide
spontaneous: false
EC number: 2.7.1.26
left: Riboflavin
left: Adenosine triphosphate
name: Adenosine triphosphate + Riboflavin → Adenosine diphosphate + Flavin Mononucleotide + Hydrogen Ion
conversion direction: LEFT_TO_RIGHT

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

Reaction1250543
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000414/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000170/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001170/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000964/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Pyrophosphate
right: FAD
spontaneous: false
left: Hydrogen Ion
left: Flavin Mononucleotide
left: Adenosine triphosphate
name: Adenosine triphosphate + Flavin Mononucleotide + Hydrogen Ion → FAD + Pyrophosphate
conversion direction: LEFT_TO_RIGHT

1.16.1.3
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000146/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000165/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001198/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000143/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/2.0
right: Riboflavin reduced
right: NADP
spontaneous: false
EC number: 1.16.1.3
left: Riboflavin
left: Hydrogen Ion
left: NADPH
name: 2 Hydrogen Ion + NADPH + Riboflavin → NADP + Riboflavin reduced
conversion direction: LEFT_TO_RIGHT

3.5.4.26
type: BiochemicalReaction
participant stoichiometry: Compound/PW C022608/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C041187/Stoichiometry/1.0
participant stoichiometry: Compound/PW C041126/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Ammonium
right: 5-Amino-6-(5'-phosphoribosylamino)uracil
spontaneous: false
EC number: 3.5.4.26
left: 2,5-Diamino-6-hydroxy-4-(5-phosphoribosylamino)pyrimidine
left: Water
left: Hydrogen Ion
name: 2,5-Diamino-6-hydroxy-4-(5-phosphoribosylamino)pyrimidine + Hydrogen Ion + Water → 5-Amino-6-(5'-phosphoribosylamino)uracil + Ammonium
conversion direction: LEFT_TO_RIGHT

Reaction1250546
type: BiochemicalReaction
participant stoichiometry: Compound/PW C041129/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/2.0
participant stoichiometry: Compound/PW C001973/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001104/Stoichiometry/1.0
participant stoichiometry: Compound/PW C006749/Stoichiometry/1.0
right: Water
right: 6,7-Dimethyl-8-(1-D-ribityl)lumazine
right: Phosphate
spontaneous: false
left: 3,4-Dihydroxy-2-butanone-4-P
left: 5-Amino-6-ribitylamino uracil
name: 3,4-Dihydroxy-2-butanone-4-P + 5-Amino-6-ribitylamino uracil → 6,7-Dimethyl-8-(1-D-ribityl)lumazine + Phosphate + 2 Water
conversion direction: LEFT_TO_RIGHT

4.1.99.12
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000092/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042619/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000479/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Hydrogen Ion
right: 1-Deoxy-L-glycero-tetrulose 4-phosphate
right: Formic acid
spontaneous: false
EC number: 4.1.99.12
left: D-Ribulose 5-phosphate
name: D-Ribulose 5-phosphate → 1-Deoxy-L-glycero-tetrulose 4-phosphate + Formic acid + Hydrogen Ion
conversion direction: LEFT_TO_RIGHT

6,7-dimethyl-8-ribityllumazine synthase
type: Complex
component stoichiometry: Protein/28020/Stoichiometry/60.0
component: Unknown

Reference/ChemSpider 431981
type: UnificationXref
id: 431981
db: ChemSpider

Compound/PW C000964 Periplasmic Space/Stoichiometry/1.0
type: Stoichiometry
physical entity: FAD
stoichiometric coefficient: 1.0

2.5.1.9
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042619/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001973/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001104/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C006749/Stoichiometry/1.0
right: Water
right: Hydrogen Ion
right: Phosphate
right: 6,7-Dimethyl-8-(1-D-ribityl)lumazine
spontaneous: false
EC number: 2.5.1.9
left: 1-Deoxy-L-glycero-tetrulose 4-phosphate
left: 5-Amino-6-ribitylamino uracil
name: 1-Deoxy-L-glycero-tetrulose 4-phosphate + 5-Amino-6-ribitylamino uracil → 6,7-Dimethyl-8-(1-D-ribityl)lumazine + Hydrogen Ion + Phosphate + Water
conversion direction: LEFT_TO_RIGHT

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

2.5.1.9
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000165/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001973/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C006749/Stoichiometry/1.0
right: Riboflavin
right: 5-Amino-6-ribitylamino uracil
spontaneous: false
EC number: 2.5.1.9
left: Hydrogen Ion
left: 6,7-Dimethyl-8-(1-D-ribityl)lumazine
name: 6,7-Dimethyl-8-(1-D-ribityl)lumazine + Hydrogen Ion → 5-Amino-6-ribitylamino uracil + Riboflavin
conversion direction: LEFT_TO_RIGHT

Pyrophosphate
type: SmallMolecule
entity reference: Pyrophosphate

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

riboflavin synthase
type: Complex
component stoichiometry: Protein/28020/Stoichiometry/3.0
component: Unknown

3.1.3.-
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001978/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001104/Stoichiometry/1.0
participant stoichiometry: Compound/PW C006749/Stoichiometry/1.0
right: Phosphate
right: 5-Amino-6-ribitylamino uracil
spontaneous: false
EC number: 3.1.3.-
left: Water
left: 5-Amino-6-(5'-phosphoribitylamino)uracil
name: 5-Amino-6-(5'-phosphoribitylamino)uracil + Water → 5-Amino-6-ribitylamino uracil + Phosphate
conversion direction: LEFT_TO_RIGHT

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

Reaction1250534
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001420/Stoichiometry/3.0
participant stoichiometry: Compound/PW C000092/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000170/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000986/Stoichiometry/1.0
participant stoichiometry: Compound/PW C041173/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/2.0
right: Hydrogen Ion
right: 2,5-Diamino-6-(5'-phosphoribosylamino)-4-pyrimidineone
right: Pyrophosphate
right: Formic acid
spontaneous: false
left: Water
left: Guanosine triphosphate
name: Guanosine triphosphate + 3 Water → 2,5-Diamino-6-(5'-phosphoribosylamino)-4-pyrimidineone + Formic acid + 2 Hydrogen Ion + Pyrophosphate
conversion direction: LEFT_TO_RIGHT

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

Reaction1250535
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000092/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000170/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000986/Stoichiometry/1.0
participant stoichiometry: Compound/PW C041126/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: 2,5-Diamino-6-hydroxy-4-(5-phosphoribosylamino)pyrimidine
right: Hydrogen Ion
right: Pyrophosphate
right: Formic acid
spontaneous: false
left: Water
left: Guanosine triphosphate
name: Guanosine triphosphate + Water → 2,5-Diamino-6-hydroxy-4-(5-phosphoribosylamino)pyrimidine + Formic acid + Hydrogen Ion + Pyrophosphate
conversion direction: LEFT_TO_RIGHT

3.5.4.26
type: BiochemicalReaction
participant stoichiometry: Compound/PW C022608/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C041187/Stoichiometry/1.0
participant stoichiometry: Compound/PW C041173/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Ammonium
right: 5-Amino-6-(5'-phosphoribosylamino)uracil
spontaneous: false
EC number: 3.5.4.26
left: Water
left: Hydrogen Ion
left: 2,5-Diamino-6-(5'-phosphoribosylamino)-4-pyrimidineone
name: 2,5-Diamino-6-(5'-phosphoribosylamino)-4-pyrimidineone + Hydrogen Ion + Water → 5-Amino-6-(5'-phosphoribosylamino)uracil + Ammonium
conversion direction: LEFT_TO_RIGHT

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

Reaction1250538
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000146/Stoichiometry/1.0
participant stoichiometry: Compound/PW C041187/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001978/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000143/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: NADP
right: 5-Amino-6-(5'-phosphoribitylamino)uracil
spontaneous: false
left: 5-Amino-6-(5'-phosphoribosylamino)uracil
left: Hydrogen Ion
left: NADPH
name: 5-Amino-6-(5'-phosphoribosylamino)uracil + Hydrogen Ion + NADPH → 5-Amino-6-(5'-phosphoribitylamino)uracil + NADP
conversion direction: LEFT_TO_RIGHT

FAD
type: SmallMolecule
entity reference: FAD

Compound/PW C001420/Stoichiometry/3.0
type: Stoichiometry
physical entity: Water
stoichiometric coefficient: 3.0

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

Riboflavin
type: SmallMolecule
entity reference: Riboflavin

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

Riboflavin
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0000244
xref: Reference/BioCyc RIBOFLAVIN
xref: Reference/ChemSpider 431981
xref: Reference/ChEBI CHEBI 17015
xref: Reference/CAS 83-88-5
xref: Reference/PubChem-compound 493570
xref: Reference/KEGG Compound C00255
chemical formula: C17H20N4O6
molecular weight: 376.13828
structure: ChemicalStructure/PW C000165

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

Compound/PW C000964/Stoichiometry/1.0
type: Stoichiometry
physical entity: FAD
stoichiometric coefficient: 1.0

fused diaminohydroxyphosphoribosylaminopyrimidine deaminase / 5-amino-6-(5-phosphoribosylamino)uracil reductase
type: Complex
component stoichiometry: Protein/28020/Stoichiometry/2.0
component: Unknown

Compound/PW C000964 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: FAD
stoichiometric coefficient: 1.0

5-Amino-6-(5'-phosphoribosylamino)uracil
type: SmallMolecule
entity reference: 5-Amino-6-(5'-phosphoribosylamino)uracil

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

Reference/ChEBI CHEBI 16238
type: UnificationXref
id: CHEBI:16238
db: ChEBI

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

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

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

Reference/PubChem-compound 439184
type: UnificationXref
id: 439184
db: PubChem-compound

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

Reference/HMDB HMDB0001520
type: UnificationXref
id: HMDB0001520
db: HMDB

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

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

Reference/ChemSpider 278
type: UnificationXref
id: 278
db: ChemSpider

Reference/ChEBI CHEBI 15934
type: UnificationXref
id: CHEBI:15934
db: ChEBI

ReactionCatalysis1281260
type: Catalysis
controller: GTP cyclohydrolase I
controlled: Reaction1250534
control type: ACTIVATION

ReactionCatalysis1281261
type: Catalysis
controller: GTP cyclohydrolase I
controlled: Reaction1250535
control type: ACTIVATION

Phosphate
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00009
xref: Reference/PubChem-compound 1061
xref: Reference/CAS 14265-44-2
xref: Reference/HMDB HMDB0001429
xref: Reference/BioCyc CPD-8587
xref: Reference/ChEBI CHEBI 18367
xref: Reference/ChemSpider 1032
chemical formula: H3O4P
molecular weight: 97.9769
structure: ChemicalStructure/PW C001104

Protein/28020/Stoichiometry/8.0
type: Stoichiometry
physical entity: Unknown
stoichiometric coefficient: 8.0

Reference/HMDB HMDB0003826
type: UnificationXref
id: HMDB0003826
db: HMDB

NADPH
type: SmallMolecule
entity reference: NADPH

Reference/PubChem-compound 6830
type: UnificationXref
id: 6830
db: PubChem-compound

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

Compound/PW C000092/Stoichiometry/1.0
type: Stoichiometry
physical entity: Formic acid
stoichiometric coefficient: 1.0

NADP
type: SmallMolecule
entity reference: NADP

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

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

2,5-Diamino-6-(5'-phosphoribosylamino)-4-pyrimidineone
type: SmallMolecule
entity reference: 2,5-Diamino-6-(5'-phosphoribosylamino)-4-pyrimidineone

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

2,5-Diamino-6-(5'-phosphoribosylamino)-4-pyrimidineone
type: SmallMoleculeReference
xref: Reference/PubChem-compound 439480
xref: Reference/ChEBI CHEBI 29114
chemical formula: C9H16N5O8P
molecular weight: 353.07364
structure: ChemicalStructure/PW C041173

2,5-Diamino-6-hydroxy-4-(5-phosphoribosylamino)pyrimidine
type: SmallMolecule
entity reference: 2,5-Diamino-6-hydroxy-4-(5-phosphoribosylamino)pyrimidine

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

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

Ammonium
type: SmallMolecule
entity reference: Ammonium

Unknown
type: Protein
entity reference: Unknown

Guanosine triphosphate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 15996
xref: Reference/ChemSpider 6569
xref: Reference/KEGG Compound C00044
xref: Reference/PubChem-compound 6830
xref: Reference/HMDB HMDB0001273
xref: Reference/CAS 86-01-1
xref: Reference/BioCyc GTP
chemical formula: C10H16N5O14P3
molecular weight: 522.99066
structure: ChemicalStructure/PW C000986

ReactionCatalysis1281271
type: Catalysis
controller: sulfite reductase
controlled: 1.16.1.3
control type: ACTIVATION

ReactionCatalysis1281270
type: Catalysis
controller: Unknown
controlled: Reaction1250543
control type: ACTIVATION

Hydrogen Ion
type: SmallMolecule
entity reference: Hydrogen Ion

ReactionCatalysis1281273
type: Catalysis
controller: fused diaminohydroxyphosphoribosylaminopyrimidine deaminase / 5-amino-6-(5-phosphoribosylamino)uracil reductase
controlled: 3.5.4.26
control type: ACTIVATION

ReactionCatalysis1281272
type: Catalysis
controller: Unknown
controlled: 1.16.1.3
control type: ACTIVATION

Transport72458
type: Transport
participant stoichiometry: Compound/PW C000964 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000964 Periplasmic Space/Stoichiometry/1.0
right: FAD
spontaneous: false
left: FAD
name: FAD (→) Transport: Prevotella copri, Cytosol to Prevotella copri, Periplasmic Space
conversion direction: LEFT_TO_RIGHT

Reference/HMDB HMDB0011106
type: UnificationXref
id: HMDB0011106
db: HMDB

FAD
type: SmallMolecule
cellular location: Periplasmic Space
entity reference: FAD

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

3,4-Dihydroxy-2-butanone-4-P
type: SmallMolecule
entity reference: 3,4-Dihydroxy-2-butanone-4-P

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

Reference/ChemSpider 216
type: UnificationXref
id: 216
db: ChemSpider

Adenosine triphosphate
type: SmallMolecule
entity reference: Adenosine triphosphate

Reference/HMDB HMDB0003841
type: UnificationXref
id: HMDB0003841
db: HMDB

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

Reference/SMPDB SMP0472925
type: UnificationXref
id: SMP0472925
db: SMPDB

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

ReactionCatalysis1281264
type: Catalysis
controller: fused diaminohydroxyphosphoribosylaminopyrimidine deaminase / 5-amino-6-(5-phosphoribosylamino)uracil reductase
controlled: Reaction1250538
control type: ACTIVATION

ReactionCatalysis1281263
type: Catalysis
controller: fused diaminohydroxyphosphoribosylaminopyrimidine deaminase / 5-amino-6-(5-phosphoribosylamino)uracil reductase
controlled: 3.5.4.26
control type: ACTIVATION

Reference/PubChem-compound 22833571
type: UnificationXref
id: 22833571
db: PubChem-compound

ReactionCatalysis1281265
type: Catalysis
controller: Unknown
controlled: 3.1.3.-
control type: ACTIVATION

ReactionCatalysis1281268
type: Catalysis
controller: riboflavin synthase
controlled: 2.5.1.9
control type: ACTIVATION

Formic acid
type: SmallMolecule
entity reference: Formic acid

ReactionCatalysis1281267
type: Catalysis
controller: 6,7-dimethyl-8-ribityllumazine synthase
controlled: 2.5.1.9
control type: ACTIVATION

ReactionCatalysis1281269
type: Catalysis
controller: Unknown
controlled: 2.7.1.26
control type: ACTIVATION

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

Reference/CAS 5118-16-1
type: UnificationXref
id: 5118-16-1
db: CAS

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

Reference/ChEBI CHEBI 18247
type: UnificationXref
id: CHEBI:18247
db: ChEBI

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

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

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

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

Reference/ChemSpider 559059
type: UnificationXref
id: 559059
db: ChemSpider

Reference/CAS 101652-10-2
type: UnificationXref
id: 101652-10-2
db: CAS

5-Amino-6-(5'-phosphoribitylamino)uracil
type: SmallMolecule
entity reference: 5-Amino-6-(5'-phosphoribitylamino)uracil

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

Reference/PathWhiz PW493844
type: UnificationXref
id: PW493844
db: PathWhiz

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

Reference/PubChem-compound 672
type: UnificationXref
id: 672
db: PubChem-compound

Reference/PubChem-compound 493570
type: UnificationXref
id: 493570
db: PubChem-compound

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

5-Amino-6-ribitylamino uracil
type: SmallMolecule
entity reference: 5-Amino-6-ribitylamino uracil

6,7-Dimethyl-8-(1-D-ribityl)lumazine
type: SmallMolecule
entity reference: 6,7-Dimethyl-8-(1-D-ribityl)lumazine

Reference/BioCyc CPD-1086
type: UnificationXref
id: CPD-1086
db: BioCyc

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

Reference/ChemSpider 326
type: UnificationXref
id: 326
db: ChemSpider

ChemicalStructure/PW C042619
type: ChemicalStructure
structure format: SMILES
structure data: CC(=O)C(O)COP(O)(O)=O

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

ChemicalStructure/PW C000143
type: ChemicalStructure
structure format: SMILES

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

Reference/ChemSpider 559060
type: UnificationXref
id: 559060
db: ChemSpider

Reference/HMDB HMDB0001557
type: UnificationXref
id: HMDB0001557
db: HMDB

ChemicalStructure/PW C000146
type: ChemicalStructure
structure format: SMILES

ReactionCatalysis1281275
type: Catalysis
controller: 3,4-dihydroxy-2-butanone 4-phosphate synthase
controlled: 4.1.99.12
control type: ACTIVATION

Compound/PW C001198/Stoichiometry/1.0
type: Stoichiometry
physical entity: Riboflavin reduced
stoichiometric coefficient: 1.0

ReactionCatalysis1281274
type: Catalysis
controller: riboflavin synthase
controlled: Reaction1250546
control type: ACTIVATION

Flavin Mononucleotide
type: SmallMolecule
entity reference: Flavin Mononucleotide

Flavin Mononucleotide
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0001520
xref: Reference/BioCyc FMN
xref: Reference/ChemSpider 559060
xref: Reference/CAS 146-17-8
xref: Reference/ChEBI CHEBI 17621
xref: Reference/PubChem-compound 643976
xref: Reference/KEGG Compound C00061
chemical formula: C17H21N4O9P
molecular weight: 456.1046
structure: ChemicalStructure/PW C001170

Reference/ChEBI CHEBI 18337
type: UnificationXref
id: CHEBI:18337
db: ChEBI

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

Reference/BioCyc CPD-316
type: UnificationXref
id: CPD-316
db: BioCyc

FAD
type: SmallMoleculeReference
xref: Reference/CAS 146-14-5
xref: Reference/HMDB HMDB0001248
xref: Reference/ChEBI CHEBI 16238
xref: Reference/BioCyc FAD
xref: Reference/PubChem-compound 643975
xref: Reference/ChemSpider 559059
xref: Reference/KEGG Compound C00016
chemical formula: C27H33N9O15P2
molecular weight: 785.1571
structure: ChemicalStructure/PW C000964

sulfite reductase
type: Complex
component stoichiometry: Protein/28020/Stoichiometry/8.0
component: Unknown

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

Reference/KEGG Compound C04732
type: UnificationXref
id: C04732
db: KEGG Compound

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

Protein/28020/Stoichiometry/60.0
type: Stoichiometry
physical entity: Unknown
stoichiometric coefficient: 60.0

Reference/PubChem-compound 221
type: UnificationXref
id: 221
db: PubChem-compound

Reference/KEGG Compound C00016
type: UnificationXref
id: C00016
db: KEGG Compound

TransportCatalysis52970
type: Catalysis
controller: Unknown
controlled: Transport72458
control type: ACTIVATION

Reference/ChEBI CHEBI 17363
type: UnificationXref
id: CHEBI:17363
db: ChEBI

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

Reference/KEGG Compound C00255
type: UnificationXref
id: C00255
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/BioCyc NAD(P)
type: UnificationXref
id: NAD(P)
db: BioCyc

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

SubPathwayInteraction520769
type: Interaction
name: SubPathway520769Reaction
name: SubPathwayReaction
participant: Guanosine triphosphate

Reference/GENE ONTOLOGY GO 0005620
type: UnificationXref
id: GO:0005620
db: GENE ONTOLOGY

Reference/ChEBI CHEBI 29114
type: UnificationXref
id: CHEBI:29114
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/PubChem-compound 333
type: UnificationXref
id: 333
db: PubChem-compound

Reference/ChEBI CHEBI 17015
type: UnificationXref
id: CHEBI:17015
db: ChEBI

2,5-Diamino-6-hydroxy-4-(5-phosphoribosylamino)pyrimidine
type: SmallMoleculeReference
xref: Reference/PubChem-compound 25244331
xref: Reference/ChEBI CHEBI 29114
chemical formula: C9H16N5O8P
molecular weight: 353.07364
structure: ChemicalStructure/PW C041126

Reference/ChEBI CHEBI 15996
type: UnificationXref
id: CHEBI:15996
db: ChEBI

3,4-Dihydroxy-2-butanone-4-P
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 50606
xref: Reference/PubChem-compound 21983291
chemical formula: C4H7O6P
molecular weight: 181.99803
structure: ChemicalStructure/PW C041129

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

ChemicalStructure/PW C000479
type: ChemicalStructure
structure format: SMILES
structure data: OCC(=O)[C@H](O)[C@H](O)COP(O)(O)=O

Protein/28020/Stoichiometry/10.0
type: Stoichiometry
physical entity: Unknown
stoichiometric coefficient: 10.0

Guanosine triphosphate
type: SmallMolecule
entity reference: Guanosine triphosphate
name: SubPathwayOutput

Reference/HMDB HMDB0000244
type: UnificationXref
id: HMDB0000244
db: HMDB

Adenosine diphosphate
type: SmallMolecule
entity reference: Adenosine diphosphate

Compound/PW C001973/Stoichiometry/1.0
type: Stoichiometry
physical entity: 6,7-Dimethyl-8-(1-D-ribityl)lumazine
stoichiometric coefficient: 1.0

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

Protein/28020/Stoichiometry/2.0
type: Stoichiometry
physical entity: Unknown
stoichiometric coefficient: 2.0

Reference/CAS 4151-19-3
type: UnificationXref
id: 4151-19-3
db: CAS

Reference/BioCyc DIMETHYL-D-RIBITYL-LUMAZINE
type: UnificationXref
id: DIMETHYL-D-RIBITYL-LUMAZINE
db: BioCyc

Prevotella copri
type: BioSource
xref: Reference/TAXONOMY 165179

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

Compound/PW C006749/Stoichiometry/1.0
type: Stoichiometry
physical entity: 5-Amino-6-ribitylamino uracil
stoichiometric coefficient: 1.0

Reference/ChEBI CHEBI 17621
type: UnificationXref
id: CHEBI:17621
db: ChEBI

Reference/KEGG Compound C01007
type: UnificationXref
id: C01007
db: KEGG Compound

ChemicalStructure/PW C000964
type: ChemicalStructure
structure format: SMILES

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

Water
type: SmallMolecule
entity reference: Water

Reference/ChemSpider 652
type: UnificationXref
id: 652
db: ChemSpider

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

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

Compound/PW C041187/Stoichiometry/1.0
type: Stoichiometry
physical entity: 5-Amino-6-(5'-phosphoribosylamino)uracil
stoichiometric coefficient: 1.0

Compound/PW C000165/Stoichiometry/1.0
type: Stoichiometry
physical entity: Riboflavin
stoichiometric coefficient: 1.0

Reference/KEGG Compound C00044
type: UnificationXref
id: C00044
db: KEGG Compound

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

ChemicalStructure/PW C001034
type: ChemicalStructure
structure format: SMILES

Reference/PubChem-compound 25244331
type: UnificationXref
id: 25244331
db: PubChem-compound

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

Protein/28020/Stoichiometry/3.0
type: Stoichiometry
physical entity: Unknown
stoichiometric coefficient: 3.0

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

Reference/PubChem-compound 18971002
type: UnificationXref
id: 18971002
db: PubChem-compound

ChemicalStructure/PW C041173
type: ChemicalStructure
structure format: SMILES

Reference/HMDB HMDB0000142
type: UnificationXref
id: HMDB0000142
db: HMDB

Reference/ChEBI CHEBI 17601
type: UnificationXref
id: CHEBI:17601
db: ChEBI

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

Reference/PubChem-compound 669
type: UnificationXref
id: 669
db: PubChem-compound

Reference/PubChem-compound 643976
type: UnificationXref
id: 643976
db: PubChem-compound

Reference/PubChem-compound 643975
type: UnificationXref
id: 643975
db: PubChem-compound

3,4-dihydroxy-2-butanone 4-phosphate synthase
type: Complex
component stoichiometry: Protein/28020/Stoichiometry/2.0
component: Unknown

5-Amino-6-ribitylamino uracil
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0011106
xref: Reference/KEGG Compound C04732
xref: Reference/ChEBI CHEBI 15934
xref: Reference/PubChem-compound 221
xref: Reference/ChemSpider 216
chemical formula: C9H16N4O6
molecular weight: 276.107
structure: ChemicalStructure/PW C006749

6,7-Dimethyl-8-(1-D-ribityl)lumazine
type: SmallMoleculeReference
xref: Reference/CAS 5118-16-1
xref: Reference/ChEBI CHEBI 17601
xref: Reference/ChemSpider 652
xref: Reference/BioCyc DIMETHYL-D-RIBITYL-LUMAZINE
xref: Reference/HMDB HMDB0003826
xref: Reference/PubChem-compound 672
xref: Reference/KEGG Compound C04332
chemical formula: C13H18N4O6
molecular weight: 326.12262
structure: ChemicalStructure/PW C001973

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

5-Amino-6-(5'-phosphoribitylamino)uracil
type: SmallMoleculeReference
xref: Reference/PubChem-compound 333
xref: Reference/ChEBI CHEBI 18247
xref: Reference/HMDB HMDB0003841
xref: Reference/KEGG Compound C04454
xref: Reference/BioCyc CPD-1086
xref: Reference/ChemSpider 326
chemical formula: C9H17N4O9P
molecular weight: 356.0733
structure: ChemicalStructure/PW C001978

Reference/KEGG Compound C00058
type: UnificationXref
id: C00058
db: KEGG Compound

Formic acid
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 30751
xref: Reference/ChemSpider 278
xref: Reference/PubChem-compound 18971002
xref: Reference/BioCyc FORMATE
xref: Reference/CAS 64-18-6
xref: Reference/KEGG Compound C00058
xref: Reference/HMDB HMDB0000142
chemical formula: CH2O2
molecular weight: 46.005478
structure: ChemicalStructure/PW C000092

Reference/CAS 83-88-5
type: UnificationXref
id: 83-88-5
db: CAS

Reference/HMDB HMDB0001248
type: UnificationXref
id: HMDB0001248
db: HMDB

Reference/KEGG Compound C00061
type: UnificationXref
id: C00061
db: KEGG Compound

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

Unknown
type: ProteinReference

ChemicalStructure/PW C041187
type: ChemicalStructure
structure format: SMILES

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

Compound/PW C041129/Stoichiometry/1.0
type: Stoichiometry
physical entity: 3,4-Dihydroxy-2-butanone-4-P
stoichiometric coefficient: 1.0

Reference/CAS 146-17-8
type: UnificationXref
id: 146-17-8
db: CAS

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

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

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

ChemicalStructure/PW C000165
type: ChemicalStructure
structure format: SMILES

Riboflavin reduced
type: SmallMolecule
entity reference: Riboflavin reduced

Riboflavin reduced
type: SmallMoleculeReference
xref: Reference/BioCyc CPD-316
xref: Reference/KEGG Compound C01007
xref: Reference/HMDB HMDB0001557
xref: Reference/CAS 101652-10-2
xref: Reference/PubChem-compound 22833571
xref: Reference/ChemSpider 17216138
chemical formula: C15H16N4O6
molecular weight: 348.107
structure: ChemicalStructure/PW C001198

GTP cyclohydrolase I
type: Complex
component stoichiometry: Protein/28020/Stoichiometry/10.0
component: Unknown

Reference/TAXONOMY 165179
type: UnificationXref
id: 165179
db: TAXONOMY

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

Compound/PW C042619/Stoichiometry/1.0
type: Stoichiometry
physical entity: 1-Deoxy-L-glycero-tetrulose 4-phosphate
stoichiometric coefficient: 1.0

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

Reference/BioCyc RIBULOSE-5P
type: UnificationXref
id: RIBULOSE-5P
db: BioCyc

Reference/PubChem-compound 439480
type: UnificationXref
id: 439480
db: PubChem-compound

Reference/KEGG Compound C00199
type: UnificationXref
id: C00199
db: KEGG Compound

1-Deoxy-L-glycero-tetrulose 4-phosphate
type: SmallMolecule
entity reference: 1-Deoxy-L-glycero-tetrulose 4-phosphate

ChemicalStructure/PW C006749
type: ChemicalStructure
structure format: SMILES

Phosphate
type: SmallMolecule
entity reference: Phosphate

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

ChemicalStructure/PW C001978
type: ChemicalStructure
structure format: SMILES

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

Reference/ChEBI CHEBI 30751
type: UnificationXref
id: CHEBI:30751
db: ChEBI

Periplasmic Space
type: CellularLocationVocabulary
xref: Reference/GENE ONTOLOGY GO 0005620

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

Reference/ChemSpider 17216138
type: UnificationXref
id: 17216138
db: ChemSpider

ChemicalStructure/PW C000092
type: ChemicalStructure
structure format: SMILES
structure data: OC=O

5-Amino-6-(5'-phosphoribosylamino)uracil
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 18337
xref: Reference/PubChem-compound 439462
chemical formula: C9H15N4O9P
molecular weight: 354.05768
structure: ChemicalStructure/PW C041187

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

ChemicalStructure/PW C041126
type: ChemicalStructure
structure format: SMILES

Reference/CAS 146-14-5
type: UnificationXref
id: 146-14-5
db: CAS

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

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

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

ChemicalStructure/PW C041129
type: ChemicalStructure
structure format: SMILES
structure data: CC(=O)C(O)COP([O-])([O-])=O

D-Ribulose 5-phosphate
type: SmallMoleculeReference
xref: Reference/CAS 4151-19-3
xref: Reference/BioCyc RIBULOSE-5P
xref: Reference/KEGG Compound C00199
xref: Reference/PubChem-compound 439184
xref: Reference/HMDB HMDB0000618
xref: Reference/ChEBI CHEBI 17363
chemical formula: C5H11O8P
molecular weight: 230.01915
structure: ChemicalStructure/PW C000479

Reference/ChemSpider 6569
type: UnificationXref
id: 6569
db: ChemSpider

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

ChemicalStructure/PW C000414
type: ChemicalStructure
structure format: SMILES

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

Compound/PW C041126/Stoichiometry/1.0
type: Stoichiometry
physical entity: 2,5-Diamino-6-hydroxy-4-(5-phosphoribosylamino)pyrimidine
stoichiometric coefficient: 1.0

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

Reference/HMDB HMDB0000618
type: UnificationXref
id: HMDB0000618
db: HMDB

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

ChemicalStructure/PW C001198
type: ChemicalStructure
structure format: SMILES

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

Reference/PubChem-compound 439462
type: UnificationXref
id: 439462
db: PubChem-compound

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

Flavin Biosynthesis
type: Pathway
pathway order: PathwaySubPathway/520769
pathway order: PathwayEnzymeReaction/6926240
pathway order: PathwayEnzymeReaction/6926242
pathway order: PathwayEnzymeReaction/6926230
pathway order: PathwayEnzymeReaction/6926241
pathway order: PathwayEnzymeReaction/6926233
pathway order: PathwayEnzymeReaction/6926244
pathway order: PathwayEnzymeReaction/6926232
pathway order: PathwayEnzymeReaction/6926243
pathway order: PathwayEnzymeReaction/6926246
pathway order: PathwayEnzymeReaction/6926234
pathway order: PathwayEnzymeReaction/6926245
pathway order: PathwayEnzymeReaction/6926237
pathway order: PathwayEnzymeReaction/6926239
pathway order: PathwayEnzymeReaction/6926238
pathway order: PathwayTransport/6926248
pathway component: ReactionCatalysis1281271
pathway component: ReactionCatalysis1281270
pathway component: ReactionCatalysis1281273
pathway component: ReactionCatalysis1281272
pathway component: 2.7.1.26
pathway component: Transport72458
pathway component: Reaction1250543
pathway component: 1.16.1.3
pathway component: 3.5.4.26
pathway component: Reaction1250546
pathway component: TransportCatalysis52970
pathway component: 4.1.99.12
pathway component: Endocytosis
pathway component: 2.5.1.9
pathway component: ReactionCatalysis1281264
pathway component: ReactionCatalysis1281263
pathway component: ReactionCatalysis1281265
pathway component: ReactionCatalysis1281268
pathway component: ReactionCatalysis1281267
pathway component: ReactionCatalysis1281269
pathway component: 3.1.3.-
pathway component: ReactionCatalysis1281260
pathway component: ReactionCatalysis1281261
pathway component: Reaction1250534
pathway component: Reaction1250535
pathway component: Reaction1250538
pathway component: ReactionCatalysis1281275
pathway component: ReactionCatalysis1281274
xref: Reference/SMPDB SMP0472925
xref: Reference/PathWhiz PW493844
organism: Prevotella copri

Reference/HMDB HMDB0001273
type: UnificationXref
id: HMDB0001273
db: HMDB

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

Compound/PW C001978/Stoichiometry/1.0
type: Stoichiometry
physical entity: 5-Amino-6-(5'-phosphoribitylamino)uracil
stoichiometric coefficient: 1.0

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

Compound/PW C001170/Stoichiometry/1.0
type: Stoichiometry
physical entity: Flavin Mononucleotide
stoichiometric coefficient: 1.0

D-Ribulose 5-phosphate
type: SmallMolecule
entity reference: D-Ribulose 5-phosphate

ChemicalStructure/PW C000986
type: ChemicalStructure
structure format: SMILES

Compound/PW C041173/Stoichiometry/1.0
type: Stoichiometry
physical entity: 2,5-Diamino-6-(5'-phosphoribosylamino)-4-pyrimidineone
stoichiometric coefficient: 1.0

Reference/CAS 64-18-6
type: UnificationXref
id: 64-18-6
db: CAS

Reference/KEGG Compound C04454
type: UnificationXref
id: C04454
db: KEGG Compound

Reference/KEGG Compound C04332
type: UnificationXref
id: C04332
db: KEGG Compound

Reference/PubChem-compound 21983291
type: UnificationXref
id: 21983291
db: PubChem-compound

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

Compound/PW C000986/Stoichiometry/1.0
type: Stoichiometry
physical entity: Guanosine triphosphate
stoichiometric coefficient: 1.0

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

Endocytosis
type: Pathway
pathway order: SubPathwayInteractionSteps/SubPathway520769
pathway component: SubPathwayInteraction520769
name: SubPathway

Compound/PW C000479/Stoichiometry/1.0
type: Stoichiometry
physical entity: D-Ribulose 5-phosphate
stoichiometric coefficient: 1.0

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

Reference/CAS 86-01-1
type: UnificationXref
id: 86-01-1
db: CAS

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

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

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

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

1-Deoxy-L-glycero-tetrulose 4-phosphate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 50608
xref: Reference/PubChem-compound 669
chemical formula: C4H9O6P
molecular weight: 184.01367
structure: ChemicalStructure/PW C042619

Compound/PW C001420/Stoichiometry/2.0
type: Stoichiometry
physical entity: Water
stoichiometric coefficient: 2.0

ChemicalStructure/PW C001973
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C001170
type: ChemicalStructure
structure format: SMILES