Compound/PW C006753/Stoichiometry/1.0
type: Stoichiometry
physical entity: Malonic semialdehyde
stoichiometric coefficient: 1.0

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

Reference/CAS 66-22-8
type: UnificationXref
id: 66-22-8
db: CAS

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

Reference/UniProt G0VQR5
type: UnificationXref
id: G0VQR5
db: UniProt

ChemicalStructure/PW C000204
type: ChemicalStructure
structure format: SMILES
structure data: O=C1NC=CC(=O)N1

an unknown oxidized electron acceptor
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 15339

Reference/PubChem-compound 123991
type: UnificationXref
id: 123991
db: PubChem-compound

an unknown reduced electron acceptor
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 17499

Peroxyaminoacrylate
type: SmallMolecule
entity reference: Peroxyaminoacrylate

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

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

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

Uracil Degradation III
type: Pathway
pathway order: PathwayEnzymeReaction/6898807
pathway order: PathwaySubPathway/517398
pathway order: PathwayEnzymeReaction/6898809
pathway order: PathwayEnzymeReaction/6898798
pathway order: PathwayEnzymeReaction/6898810
pathway order: PathwayEnzymeReaction/6898811
pathway order: PathwayEnzymeReaction/6898803
pathway order: PathwayEnzymeReaction/6898806
pathway component: 1.-.-.-
pathway component: ReactionCatalysis1265288
pathway component: ReactionCatalysis1265296
pathway component: ReactionCatalysis1265294
pathway component: ReactionCatalysis1265295
pathway component: Reaction5907
pathway component: ReactionCatalysis1265290
pathway component: ReactionCatalysis1265291
pathway component: Purine Degradation
pathway component: 1.1.1.-
pathway component: 3.5.1.-
pathway component: 1.14.99.46
pathway component: 3.5.1.110
xref: Reference/SMPDB SMP0645527
xref: Reference/PathWhiz PW685872
organism: Megasphaera elsdenii DSM 20460

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

3-oxoacyl-[acyl-carrier-protein] reductase
type: ProteinReference
xref: Reference/UniProt G0VR49

Carbamic acid
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 28616
xref: Reference/KEGG Compound C01563
xref: Reference/ChemSpider 271
xref: Reference/PubChem-compound 277
xref: Reference/HMDB HMDB0003551
xref: Reference/CAS 463-77-4
chemical formula: CH3NO2
molecular weight: 61.016376
structure: ChemicalStructure/PW C001922

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

Reference/HMDB HMDB0000300
type: UnificationXref
id: HMDB0000300
db: HMDB

Putative endoribonuclease L-PSP
type: Protein
entity reference: Putative endoribonuclease L-PSP

Hydroxylamine reductase
type: Protein
entity reference: Hydroxylamine reductase

Putative oligopeptide transporter permease
type: ProteinReference
xref: Reference/UniProt G0VQH6

NAD(P)H-flavin oxidoreductase
type: Protein
entity reference: NAD(P)H-flavin oxidoreductase

SubPathwayInteraction517398
type: Interaction
name: SubPathwayReaction
name: SubPathway517398Reaction
participant: Uracil

Putative endoribonuclease L-PSP
type: ProteinReference
xref: Reference/UniProt G0VPX1

NAD(P)H-flavin oxidoreductase
type: ProteinReference
xref: Reference/UniProt G0VRH8

Reference/ChEBI CHEBI 17568
type: UnificationXref
id: CHEBI:17568
db: ChEBI

Hydroxylamine reductase
type: ProteinReference
xref: Reference/UniProt G0VN26

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

Carbamic acid
type: SmallMolecule
entity reference: Carbamic acid

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

3-oxoacyl-[acyl-carrier-protein] reductase
type: Protein
entity reference: 3-oxoacyl-[acyl-carrier-protein] reductase

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

Reference/ChemSpider 1141
type: UnificationXref
id: 1141
db: ChemSpider

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

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

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

ChemicalStructure/PW C000552
type: ChemicalStructure
structure format: SMILES
structure data: OCCC(O)=O

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

Reference/ChemSpider 271
type: UnificationXref
id: 271
db: ChemSpider

Reference/CAS 463-77-4
type: UnificationXref
id: 463-77-4
db: CAS

Reference/KEGG Compound C00106
type: UnificationXref
id: C00106
db: KEGG Compound

Reference/UniProt G0VR49
type: UnificationXref
id: G0VR49
db: UniProt

Reference/PubChem-compound 445395
type: UnificationXref
id: 445395
db: PubChem-compound

Peroxyaminoacrylate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 59892
xref: Reference/PubChem-compound 46173085
chemical formula: C3H5NO3
molecular weight: 103.02694
structure: ChemicalStructure/PW C041602

NADPH
type: SmallMolecule
entity reference: NADPH

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

Reference/KEGG Compound C00222
type: UnificationXref
id: C00222
db: KEGG Compound

Reference/CAS 1948-56-7
type: UnificationXref
id: 1948-56-7
db: CAS

NADP
type: SmallMolecule
entity reference: NADP

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

Reference/CAS 5666-16-0
type: UnificationXref
id: 5666-16-0
db: CAS

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

1.-.-.-
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040968/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040969/Stoichiometry/1.0
participant stoichiometry: Compound/PW C044507/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001938/Stoichiometry/1.0
right: 2-Aminoacrylic acid
right: an unknown oxidized electron acceptor
spontaneous: false
EC number: 1.-.-.-
left: an unknown reduced electron acceptor
left: 3-Aminoacrylate
name: 3-Aminoacrylate + an unknown reduced electron acceptor → 2-Aminoacrylic acid + an unknown oxidized electron acceptor
conversion direction: LEFT_TO_RIGHT

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

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

Ammonium
type: SmallMolecule
entity reference: Ammonium

Hydrogen Ion
type: SmallMolecule
entity reference: Hydrogen Ion

Reference/KEGG Compound C01563
type: UnificationXref
id: C01563
db: KEGG Compound

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

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

Reference/CAS 503-66-2
type: UnificationXref
id: 503-66-2
db: CAS

Malonic semialdehyde
type: SmallMolecule
entity reference: Malonic semialdehyde

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

FMNH2
type: SmallMolecule
entity reference: FMNH2

Oxygen
type: SmallMolecule
entity reference: Oxygen

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

1.1.1.-
type: BiochemicalReaction
participant stoichiometry: Compound/PW C006753/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000146/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000143/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000552/Stoichiometry/1.0
right: Hydroxypropionic acid
right: NADP
spontaneous: false
EC number: 1.1.1.-
left: Malonic semialdehyde
left: Hydrogen Ion
left: NADPH
name: Hydrogen Ion + Malonic semialdehyde + NADPH → Hydroxypropionic acid + NADP
conversion direction: LEFT_TO_RIGHT

3.5.1.-
type: BiochemicalReaction
participant stoichiometry: Compound/PW C006753/Stoichiometry/1.0
participant stoichiometry: Compound/PW C022608/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001938/Stoichiometry/1.0
right: Malonic semialdehyde
right: Ammonium
spontaneous: false
EC number: 3.5.1.-
left: Water
left: 2-Aminoacrylic acid
left: Hydrogen Ion
name: 2-Aminoacrylic acid + Hydrogen Ion + Water → Ammonium + Malonic semialdehyde
conversion direction: LEFT_TO_RIGHT

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

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

Compound/PW C040968/Stoichiometry/1.0
type: Stoichiometry
physical entity: an unknown oxidized electron acceptor
stoichiometric coefficient: 1.0

ReactionCatalysis1265296
type: Catalysis
controller: Putative oligopeptide transporter permease
controlled: 3.5.1.110
control type: ACTIVATION

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

ReactionCatalysis1265294
type: Catalysis
controller: Putative endoribonuclease L-PSP
controlled: 1.-.-.-
control type: ACTIVATION

ReactionCatalysis1265295
type: Catalysis
controller: Putative TRK potassium uptake system protein
controlled: 1.14.99.46
control type: ACTIVATION

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

Reference/HMDB HMDB0003609
type: UnificationXref
id: HMDB0003609
db: HMDB

ReactionCatalysis1265290
type: Catalysis
controller: 3-hydroxy acid dehydrogenase
controlled: 1.1.1.-
control type: ACTIVATION

ReactionCatalysis1265291
type: Catalysis
controller: NAD(P)H-flavin oxidoreductase
controlled: 1.1.1.-
control type: ACTIVATION

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

3-Aminoacrylate
type: SmallMolecule
entity reference: 3-Aminoacrylate

Reference/HMDB HMDB0011111
type: UnificationXref
id: HMDB0011111
db: HMDB

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

Protein/31255/Stoichiometry/4.0
type: Stoichiometry
physical entity: 3-oxoacyl-[acyl-carrier-protein] reductase
stoichiometric coefficient: 4.0

ChemicalStructure/PW C000146
type: ChemicalStructure
structure format: SMILES

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

1.14.99.46
type: BiochemicalReaction
participant stoichiometry: Compound/PW C041602/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001065/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000204/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000891/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001170/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Hydrogen Ion
right: Flavin Mononucleotide
right: Peroxyaminoacrylate
spontaneous: false
EC number: 1.14.99.46
left: FMNH2
left: Oxygen
left: Uracil
name: FMNH2 + Oxygen + Uracil → Flavin Mononucleotide + Hydrogen Ion + Peroxyaminoacrylate
conversion direction: LEFT_TO_RIGHT

3.5.1.110
type: BiochemicalReaction
participant stoichiometry: Compound/PW C041602/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001922/Stoichiometry/1.0
participant stoichiometry: Compound/PW C044507/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Hydrogen Ion
right: Carbamic acid
right: 3-Aminoacrylate
spontaneous: false
EC number: 3.5.1.110
left: Water
left: Peroxyaminoacrylate
name: Peroxyaminoacrylate + Water → 3-Aminoacrylate + Carbamic acid + Hydrogen Ion
conversion direction: LEFT_TO_RIGHT

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

2-Aminoacrylic acid
type: SmallMoleculeReference
xref: Reference/ChemSpider 110510
xref: Reference/CAS 1948-56-7
xref: Reference/KEGG Compound C02218
xref: Reference/HMDB HMDB0003609
xref: Reference/PubChem-compound 123991
xref: Reference/ChEBI CHEBI 17123
chemical formula: C3H5NO2
molecular weight: 87.03203
structure: ChemicalStructure/PW C001938

ReactionCatalysis1265288
type: Catalysis
controller: Hydroxylamine reductase
controlled: 3.5.1.-
control type: ACTIVATION

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

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

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

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

3-Aminoacrylate
type: SmallMoleculeReference
xref: Reference/KEGG Compound C20253
xref: Reference/PubChem-compound 46173135
xref: Reference/ChEBI CHEBI 59894
chemical formula: C3H5NO2
molecular weight: 87.03203
structure: ChemicalStructure/PW C044507

Reference/ChEBI CHEBI 17123
type: UnificationXref
id: CHEBI:17123
db: ChEBI

Putative oligopeptide transporter permease
type: Protein
entity reference: Putative oligopeptide transporter permease

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

Purine Degradation
type: Pathway
pathway order: SubPathwayInteractionSteps/SubPathway517398
pathway component: SubPathwayInteraction517398
xref: Reference/SMPDB SMP0001901
xref: Reference/PathWhiz PW001887
name: SubPathway

Reference/ChEBI CHEBI 16048
type: UnificationXref
id: CHEBI:16048
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/ChEBI CHEBI 17499
type: UnificationXref
id: CHEBI:17499
db: ChEBI

Reference/ChEBI CHEBI 59892
type: UnificationXref
id: CHEBI:59892
db: ChEBI

an unknown oxidized electron acceptor
type: SmallMolecule
entity reference: an unknown oxidized electron acceptor

an unknown reduced electron acceptor
type: SmallMolecule
entity reference: an unknown reduced electron acceptor

Reference/ChEBI CHEBI 59894
type: UnificationXref
id: CHEBI:59894
db: ChEBI

Compound/PW C041602/Stoichiometry/1.0
type: Stoichiometry
physical entity: Peroxyaminoacrylate
stoichiometric coefficient: 1.0

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

Reference/UniProt G0VRH8
type: UnificationXref
id: G0VRH8
db: UniProt

ChemicalStructure/PW C001938
type: ChemicalStructure
structure format: SMILES
structure data: NC(=C)C(O)=O

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

Compound/PW C001922/Stoichiometry/1.0
type: Stoichiometry
physical entity: Carbamic acid
stoichiometric coefficient: 1.0

Reference/KEGG Compound C02218
type: UnificationXref
id: C02218
db: KEGG Compound

Putative TRK potassium uptake system protein
type: ProteinReference
xref: Reference/UniProt G0VQR5

Reference/PathWhiz PW685872
type: UnificationXref
id: PW685872
db: PathWhiz

Water
type: SmallMolecule
entity reference: Water

Reference/UniProt G0VPX1
type: UnificationXref
id: G0VPX1
db: UniProt

Compound/PW C000891/Stoichiometry/1.0
type: Stoichiometry
physical entity: FMNH2
stoichiometric coefficient: 1.0

Hydroxypropionic acid
type: SmallMoleculeReference
xref: Reference/PubChem-compound 68152
xref: Reference/ChemSpider 61460
xref: Reference/ChEBI CHEBI 33404
xref: Reference/HMDB HMDB0000700
xref: Reference/KEGG Compound C01013
xref: Reference/CAS 503-66-2
chemical formula: C3H6O3
molecular weight: 90.03169
structure: ChemicalStructure/PW C000552

Reference/SMPDB SMP0645527
type: UnificationXref
id: SMP0645527
db: SMPDB

ChemicalStructure/PW C041602
type: ChemicalStructure
structure format: SMILES
structure data: N\C=C/C(=O)OO

Reference/SMPDB SMP0001901
type: UnificationXref
id: SMP0001901
db: SMPDB

Reference/ChEBI CHEBI 15339
type: UnificationXref
id: CHEBI:15339
db: ChEBI

Reference/KEGG Compound C01013
type: UnificationXref
id: C01013
db: KEGG Compound

Uracil
type: SmallMolecule
entity reference: Uracil
name: SubPathwayOutput

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

Reference/UniProt G0VN26
type: UnificationXref
id: G0VN26
db: UniProt

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

Reference/HMDB HMDB0000700
type: UnificationXref
id: HMDB0000700
db: HMDB

Reference/UniProt G0VQH6
type: UnificationXref
id: G0VQH6
db: UniProt

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

Compound/PW C000204/Stoichiometry/1.0
type: Stoichiometry
physical entity: Uracil
stoichiometric coefficient: 1.0

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

Reference/PubChem-compound 46173135
type: UnificationXref
id: 46173135
db: PubChem-compound

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

Reference/ChEBI CHEBI 17960
type: UnificationXref
id: CHEBI:17960
db: ChEBI

Malonic semialdehyde
type: SmallMoleculeReference
xref: Reference/CAS 926-61-4
xref: Reference/PubChem-compound 868
xref: Reference/ChEBI CHEBI 17960
xref: Reference/ChemSpider 845
xref: Reference/HMDB HMDB0011111
xref: Reference/KEGG Compound C00222
chemical formula: C3H4O3
molecular weight: 88.016045
structure: ChemicalStructure/PW C006753

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

Hydroxypropionic acid
type: SmallMolecule
entity reference: Hydroxypropionic acid

Reference/CAS 926-61-4
type: UnificationXref
id: 926-61-4
db: CAS

Reference/ChEBI CHEBI 33404
type: UnificationXref
id: CHEBI:33404
db: ChEBI

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

FMNH2
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 16048
xref: Reference/BioCyc FMNH2
xref: Reference/KEGG Compound C01847
xref: Reference/PubChem-compound 445395
xref: Reference/CAS 5666-16-0
xref: Reference/ChemSpider 393046
xref: Reference/HMDB HMDB0001142
chemical formula: C17H23N4O9P
molecular weight: 458.12027
structure: ChemicalStructure/PW C000891

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

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

Reference/PathWhiz PW001887
type: UnificationXref
id: PW001887
db: PathWhiz

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

ChemicalStructure/PW C001922
type: ChemicalStructure
structure format: SMILES
structure data: NC(O)=O

Reaction5907
type: BiochemicalReaction
participant stoichiometry: Compound/PW C022608/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001316/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001922/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/2.0
right: Ammonium
right: Carbon dioxide
spontaneous: false
left: Hydrogen Ion
left: Carbamic acid
name: Carbamic acid + 2 Hydrogen Ion → Ammonium + Carbon dioxide
conversion direction: LEFT_TO_RIGHT

Compound/PW C044507/Stoichiometry/1.0
type: Stoichiometry
physical entity: 3-Aminoacrylate
stoichiometric coefficient: 1.0

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

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

Reference/ChEBI CHEBI 28616
type: UnificationXref
id: CHEBI:28616
db: ChEBI

Reference/HMDB HMDB0003551
type: UnificationXref
id: HMDB0003551
db: HMDB

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

ChemicalStructure/PW C044507
type: ChemicalStructure
structure format: SMILES
structure data: N\C=C/C(O)=O

Reference/KEGG Compound C01847
type: UnificationXref
id: C01847
db: KEGG 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

Reference/PubChem-compound 1174
type: UnificationXref
id: 1174
db: PubChem-compound

ChemicalStructure/PW C000891
type: ChemicalStructure
structure format: SMILES

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

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

ChemicalStructure/PW C006753
type: ChemicalStructure
structure format: SMILES
structure data: OC(=O)CC=O

Megasphaera elsdenii DSM 20460
type: BioSource
xref: Reference/TAXONOMY 1064535

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

Reference/HMDB HMDB0001142
type: UnificationXref
id: HMDB0001142
db: HMDB

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

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+]

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

Reference/PubChem-compound 277
type: UnificationXref
id: 277
db: PubChem-compound

Reference/ChemSpider 845
type: UnificationXref
id: 845
db: ChemSpider

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

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

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

Reference/PubChem-compound 46173085
type: UnificationXref
id: 46173085
db: PubChem-compound

Reference/PubChem-compound 868
type: UnificationXref
id: 868
db: PubChem-compound

Uracil
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 17568
xref: Reference/KEGG Compound C00106
xref: Reference/HMDB HMDB0000300
xref: Reference/CAS 66-22-8
xref: Reference/BioCyc URACIL
xref: Reference/PubChem-compound 1174
xref: Reference/ChemSpider 1141
chemical formula: C4H4N2O2
molecular weight: 112.027275
structure: ChemicalStructure/PW C000204

3-hydroxy acid dehydrogenase
type: Complex
component stoichiometry: Protein/31255/Stoichiometry/4.0
component: 3-oxoacyl-[acyl-carrier-protein] reductase

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

Compound/PW C001938/Stoichiometry/1.0
type: Stoichiometry
physical entity: 2-Aminoacrylic acid
stoichiometric coefficient: 1.0

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

Reference/BioCyc FMNH2
type: UnificationXref
id: FMNH2
db: BioCyc

Water
type: SmallMoleculeReference
xref: Reference/PubChem-compound 962
xref: Reference/ChEBI CHEBI 15377
xref: Reference/KEGG Compound C00001
xref: Reference/ChemSpider 937
xref: Reference/HMDB HMDB0002111
xref: Reference/CAS 7732-18-5
chemical formula: H2O
molecular weight: 18.010565
structure: ChemicalStructure/PW C001420

Reference/ChemSpider 393046
type: UnificationXref
id: 393046
db: ChemSpider

Compound/PW C040969/Stoichiometry/1.0
type: Stoichiometry
physical entity: an unknown reduced electron acceptor
stoichiometric coefficient: 1.0

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

Reference/KEGG Compound C20253
type: UnificationXref
id: C20253
db: KEGG Compound

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

Carbon dioxide
type: SmallMolecule
entity reference: Carbon dioxide

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

Reference/TAXONOMY 1064535
type: UnificationXref
id: 1064535
db: TAXONOMY

Reference/ChemSpider 110510
type: UnificationXref
id: 110510
db: ChemSpider

Reference/PubChem-compound 68152
type: UnificationXref
id: 68152
db: PubChem-compound

Reference/ChemSpider 61460
type: UnificationXref
id: 61460
db: ChemSpider

Compound/PW C000552/Stoichiometry/1.0
type: Stoichiometry
physical entity: Hydroxypropionic acid
stoichiometric coefficient: 1.0

Putative TRK potassium uptake system protein
type: Protein
entity reference: Putative TRK potassium uptake system protein

ChemicalStructure/PW C001170
type: ChemicalStructure
structure format: SMILES