Compound/PW C040959/Stoichiometry/1.0
type: Stoichiometry
physical entity: keto-L-rhamnulose
stoichiometric coefficient: 1.0

α-L-rhamnopyranose
type: SmallMolecule
cellular location: Cytosol
entity reference: α-L-rhamnopyranose

L-rhamnulofuranose
type: SmallMoleculeReference
chemical formula: C6H12O5
molecular weight: 164.06847
structure: ChemicalStructure/PW C040960

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

L-rhamnulose 1-phosphate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 58313
chemical formula: C9H19O5P
molecular weight: 238.09702
structure: ChemicalStructure/PW C040961

Unknown
type: Protein
entity reference: Unknown

(S)-lactaldehyde
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 18041
chemical formula: C3H6O2
molecular weight: 74.03678
structure: ChemicalStructure/PW C040962

Protein/28065/Stoichiometry/4.0
type: Stoichiometry
physical entity: Unknown
stoichiometric coefficient: 4.0

L-rhamnose 1-epimerase
type: ProteinReference
xref: Reference/UniProt B3CEI2

L-rhamnose isomerase
type: ProteinReference

Compound/PW C040961/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-rhamnulose 1-phosphate
stoichiometric coefficient: 1.0

L-fuculose 1-phosphate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 57846
chemical formula: C6H11O8P
molecular weight: 242.02025
structure: ChemicalStructure/PW C040963

Rhamnulokinase
type: ProteinReference

L-fuculose
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 17617
chemical formula: C6H12O5
molecular weight: 164.06847
structure: ChemicalStructure/PW C040964

Reference/ChEBI CHEBI 42548
type: UnificationXref
id: CHEBI:42548
db: ChEBI

α-L-fucopyranose
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 42548
chemical formula: C6H12O5
molecular weight: 164.06847
structure: ChemicalStructure/PW C040965

β-L-fucopyranose
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 42589
xref: Reference/HMDB HMDB0124735
chemical formula: C6H12O5
molecular weight: 164.06847
structure: ChemicalStructure/PW C040966

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

(S)-Propane-1,2-diol
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 29002
chemical formula: C3H8O2
molecular weight: 76.05243
structure: ChemicalStructure/PW C040967

Reference/ChemSpider 96860
type: UnificationXref
id: 96860
db: ChemSpider

L-fuculose-phosphate aldolase
type: Complex
component stoichiometry: Protein/28065/Stoichiometry/4.0
component: Unknown

Compound/PW C040960/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-rhamnulofuranose
stoichiometric coefficient: 1.0

aldehyde dehydrogenase A, NAD-linked
type: Complex
component stoichiometry: Protein/28065/Stoichiometry/4.0
component: Unknown

NADH
type: SmallMolecule
entity reference: NADH

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

L-fucose isomerase
type: Complex
component stoichiometry: Protein/28065/Stoichiometry/6.0
component: Unknown

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

Putative rhamnulose-1-phosphate aldolase
type: ProteinReference
xref: Reference/UniProt B3C6Q9

L-fucose mutarotase
type: Complex
component stoichiometry: Protein/56326/Stoichiometry/6.0
component: SusC/RagA family TonB-linked outer membrane protein

SusC/RagA family TonB-linked outer membrane protein
type: ProteinReference

rhamnulose-1-phosphate aldolase
type: Complex
component stoichiometry: Protein/56325/Stoichiometry/4.0
component: Putative rhamnulose-1-phosphate aldolase

L-rhamnose isomerase
type: Complex
component stoichiometry: Protein/56323/Stoichiometry/4.0
component: L-rhamnose isomerase

L-rhamnose mutarotase
type: Complex
component stoichiometry: Protein/28065/Stoichiometry/2.0
component: Unknown

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

Compound/PW C040962/Stoichiometry/1.0
type: Stoichiometry
physical entity: (S)-lactaldehyde
stoichiometric coefficient: 1.0

Reduced acceptor
type: SmallMolecule
entity reference: Reduced acceptor

Compound/PW C040958/Stoichiometry/1.0
type: Stoichiometry
physical entity: β-L-rhamnopyranose
stoichiometric coefficient: 1.0

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

NAD
type: SmallMolecule
entity reference: NAD

SubPathwayInteraction427460
type: Interaction
name: SubPathway427460Reaction
name: SubPathwayReaction
participant: Pyruvic acid

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

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

Dihydroxyacetone phosphate
type: SmallMolecule
entity reference: Dihydroxyacetone phosphate

1.2.1.22
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001420/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040962/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000721/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000122/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001144/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/2.0
right: NADH
right: L-Lactic acid
right: Hydrogen Ion
spontaneous: false
EC number: 1.2.1.22
left: Water
left: (S)-lactaldehyde
left: NAD
name: (S)-lactaldehyde + NAD + Water → 2 Hydrogen Ion + L-Lactic acid + NADH
conversion direction: LEFT_TO_RIGHT

Compound/PW C040957/Stoichiometry/1.0
type: Stoichiometry
physical entity: α-L-rhamnopyranose
stoichiometric coefficient: 1.0

Dihydroxyacetone phosphate
type: SmallMoleculeReference
xref: Reference/BioCyc DIHYDROXY-ACETONE-PHOSPHATE
xref: Reference/PubChem-compound 668
xref: Reference/ChEBI CHEBI 16108
xref: Reference/KEGG Compound C00111
xref: Reference/CAS 57-04-5
xref: Reference/ChemSpider 648
xref: Reference/HMDB HMDB0001473
chemical formula: C3H7O6P
molecular weight: 169.99803
structure: ChemicalStructure/PW C001134

Pyruvic acid
type: SmallMolecule
entity reference: Pyruvic acid
name: SubPathwayInput

Compound/PW C040957 Periplasmic Space/Stoichiometry/1.0
type: Stoichiometry
physical entity: α-L-rhamnopyranose
stoichiometric coefficient: 1.0

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

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

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

SubPathwayInteraction427459
type: Interaction
name: SubPathwayReaction
name: SubPathway427459Reaction
participant: Dihydroxyacetone phosphate

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/ChEBI CHEBI 15022
type: UnificationXref
id: CHEBI:15022
db: ChEBI

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

Reference/PathWhiz PW423994
type: UnificationXref
id: PW423994
db: PathWhiz

Fucose and Rhamnose Degradation
type: Pathway
pathway order: PathwayEnzymeReaction/5997657
pathway order: PathwayEnzymeReaction/5997658
pathway order: PathwayEnzymeReaction/5997655
pathway order: PathwayEnzymeReaction/5997667
pathway order: PathwayEnzymeReaction/5997653
pathway order: PathwayEnzymeReaction/5997654
pathway order: PathwayEnzymeReaction/5997651
pathway order: PathwayEnzymeReaction/5997652
pathway order: PathwayEnzymeReaction/5997663
pathway order: PathwayEnzymeReaction/5997660
pathway order: PathwayEnzymeReaction/5997650
pathway order: PathwayEnzymeReaction/5997661
pathway order: PathwaySubPathway/427459
pathway order: PathwayTransport/5997672
pathway order: PathwayTransport/5997668
pathway order: PathwaySubPathway/427460
pathway component: Glycolysis and Pyruvate Dehydrogenase
pathway component: Reaction2969
pathway component: 2.7.1.5
pathway component: 4.1.2.19
pathway component: TransportCatalysis38499
pathway component: TransportCatalysis38498
pathway component: ReactionCatalysis851697
pathway component: ReactionCatalysis851698
pathway component: 5.1.3.32
pathway component: ReactionCatalysis851699
pathway component: ReactionCatalysis851710
pathway component: 5.3.1.14
pathway component: Fructose Metabolism
pathway component: ReactionCatalysis491408
pathway component: 1.1.-.-
pathway component: 4.1.2.17
pathway component: 2.7.1.51
pathway component: 5.3.1.25
pathway component: 1.2.1.22
pathway component: 5.1.3.29
pathway component: 1.1.1.77
pathway component: ReactionCatalysis851700
pathway component: ReactionCatalysis851701
pathway component: ReactionCatalysis851702
pathway component: Transport57563
pathway component: ReactionCatalysis851703
pathway component: Transport57562
pathway component: ReactionCatalysis851705
pathway component: ReactionCatalysis851707
xref: Reference/PathWhiz PW423994
xref: Reference/SMPDB SMP0411615
organism: Bacteroides intestinalis

Compound/PW C000122/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Lactic acid
stoichiometric coefficient: 1.0

ReactionCatalysis851710
type: Catalysis
controller: Unknown
controlled: 1.1.-.-
control type: ACTIVATION

Lactaldehyde reductase
type: ProteinReference

Compound/PW C040963/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-fuculose 1-phosphate
stoichiometric coefficient: 1.0

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

Compound/PW C040965/Stoichiometry/1.0
type: Stoichiometry
physical entity: α-L-fucopyranose
stoichiometric coefficient: 1.0

Reference/TAXONOMY 329854
type: UnificationXref
id: 329854
db: TAXONOMY

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

ReactionCatalysis851700
type: Catalysis
controller: rhamnulose-1-phosphate aldolase
controlled: 4.1.2.19
control type: ACTIVATION

ReactionCatalysis851701
type: Catalysis
controller: L-fuculose-phosphate aldolase
controlled: 4.1.2.17
control type: ACTIVATION

ReactionCatalysis851702
type: Catalysis
controller: Unknown
controlled: 2.7.1.51
control type: ACTIVATION

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

ReactionCatalysis851703
type: Catalysis
controller: L-fucose isomerase
controlled: 5.3.1.25
control type: ACTIVATION

β-L-rhamnopyranose
type: SmallMolecule
cellular location: Periplasmic Space
entity reference: β-L-rhamnopyranose

ReactionCatalysis851705
type: Catalysis
controller: L-fucose mutarotase
controlled: 5.1.3.29
control type: ACTIVATION

ReactionCatalysis851707
type: Catalysis
controller: L-1,2-propanediol oxidoreductase
controlled: 1.1.1.77
control type: ACTIVATION

Hydrogen Ion
type: SmallMolecule
entity reference: Hydrogen Ion

Reference/PathWhiz PW000785
type: UnificationXref
id: PW000785
db: PathWhiz

Protein/28065/Stoichiometry/6.0
type: Stoichiometry
physical entity: Unknown
stoichiometric coefficient: 6.0

α-L-rhamnopyranose
type: SmallMolecule
entity reference: α-L-rhamnopyranose

Reference/KEGG Compound C00111
type: UnificationXref
id: C00111
db: KEGG Compound

β-L-rhamnopyranose
type: SmallMolecule
entity reference: β-L-rhamnopyranose

keto-L-rhamnulose
type: SmallMolecule
entity reference: keto-L-rhamnulose

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

Adenosine triphosphate
type: SmallMolecule
entity reference: Adenosine triphosphate

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

Protein/56323/Stoichiometry/4.0
type: Stoichiometry
physical entity: L-rhamnose isomerase
stoichiometric coefficient: 4.0

Putative rhamnulose-1-phosphate aldolase
type: Protein
entity reference: Putative rhamnulose-1-phosphate aldolase

ReactionCatalysis491408
type: Catalysis
controller: aldehyde dehydrogenase A, NAD-linked
controlled: 1.2.1.22
control type: ACTIVATION

Rhamnulokinase
type: Protein
entity reference: Rhamnulokinase

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

L-rhamnose isomerase
type: Protein
entity reference: L-rhamnose isomerase

L-rhamnose 1-epimerase
type: Protein
entity reference: L-rhamnose 1-epimerase

Lactaldehyde reductase
type: Protein
entity reference: Lactaldehyde reductase

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

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

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

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

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

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

SusC/RagA family TonB-linked outer membrane protein
type: Protein
entity reference: SusC/RagA family TonB-linked outer membrane protein

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

Compound/PW C040967/Stoichiometry/1.0
type: Stoichiometry
physical entity: (S)-Propane-1,2-diol
stoichiometric coefficient: 1.0

Reference/CAS 57-04-5
type: UnificationXref
id: 57-04-5
db: CAS

Reference/ChEBI CHEBI 29002
type: UnificationXref
id: CHEBI:29002
db: ChEBI

Reference/UniProt B3C6Q9
type: UnificationXref
id: B3C6Q9
db: UniProt

Glycolysis and Pyruvate Dehydrogenase
type: Pathway
pathway order: SubPathwayInteractionSteps/SubPathway427460
pathway component: SubPathwayInteraction427460
xref: Reference/PathWhiz PW000785
xref: Reference/SMPDB SMP0000807
name: SubPathway

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

NAD
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 15846
xref: Reference/HMDB HMDB0000902
xref: Reference/CAS 53-84-9
xref: Reference/KEGG Compound C00003
xref: Reference/PubChem-compound 5893
xref: Reference/BioCyc NAD
xref: Reference/ChemSpider 5682
chemical formula: C21H27N7O14P2
molecular weight: 663.10913
structure: ChemicalStructure/PW C000721

Reference/PubChem-compound 107689
type: UnificationXref
id: 107689
db: PubChem-compound

Reaction2969
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040960/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040959/Stoichiometry/1.0
right: L-rhamnulofuranose
spontaneous: true
left: keto-L-rhamnulose
name: keto-L-rhamnulose → L-rhamnulofuranose
conversion direction: LEFT_TO_RIGHT

Compound/PW C040964/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-fuculose
stoichiometric coefficient: 1.0

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

Reference/ChEBI CHEBI 58313
type: UnificationXref
id: CHEBI:58313
db: ChEBI

Protein/56326/Stoichiometry/6.0
type: Stoichiometry
physical entity: SusC/RagA family TonB-linked outer membrane protein
stoichiometric coefficient: 6.0

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

α-L-rhamnopyranose
type: SmallMolecule
cellular location: Periplasmic Space
entity reference: α-L-rhamnopyranose

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

Compound/PW C040958 Periplasmic Space/Stoichiometry/1.0
type: Stoichiometry
physical entity: β-L-rhamnopyranose
stoichiometric coefficient: 1.0

Unknown
type: ProteinReference

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

Fructose Metabolism
type: Pathway
pathway order: SubPathwayInteractionSteps/SubPathway427459
pathway component: SubPathwayInteraction427459
xref: Reference/SMPDB SMP0000930
xref: Reference/PathWhiz PW000913
name: SubPathway

L-rhamnulofuranose
type: SmallMolecule
entity reference: L-rhamnulofuranose

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

L-rhamnulose 1-phosphate
type: SmallMolecule
entity reference: L-rhamnulose 1-phosphate

(S)-lactaldehyde
type: SmallMolecule
entity reference: (S)-lactaldehyde

L-fuculose 1-phosphate
type: SmallMolecule
entity reference: L-fuculose 1-phosphate

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

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

α-L-rhamnopyranose
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 27907
chemical formula: C6H12O5
molecular weight: 164.06847
structure: ChemicalStructure/PW C040957

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

β-L-rhamnopyranose
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 27586
chemical formula: C6H12O5
molecular weight: 164.06847
structure: ChemicalStructure/PW C040958

L-fuculose
type: SmallMolecule
entity reference: L-fuculose

keto-L-rhamnulose
type: SmallMoleculeReference
chemical formula: C6H12O5
molecular weight: 164.06847
structure: ChemicalStructure/PW C040959

α-L-fucopyranose
type: SmallMolecule
entity reference: α-L-fucopyranose

β-L-fucopyranose
type: SmallMolecule
entity reference: β-L-fucopyranose

(S)-Propane-1,2-diol
type: SmallMolecule
entity reference: (S)-Propane-1,2-diol

Adenosine diphosphate
type: SmallMolecule
entity reference: Adenosine diphosphate

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

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

ChemicalStructure/PW C000122
type: ChemicalStructure
structure format: SMILES
structure data: C[C@H](O)C(O)=O

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

ChemicalStructure/PW C000721
type: ChemicalStructure
structure format: SMILES

Reference/SMPDB SMP0000807
type: UnificationXref
id: SMP0000807
db: SMPDB

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

ChemicalStructure/PW C001144
type: ChemicalStructure
structure format: SMILES

TransportCatalysis38499
type: Catalysis
controller: L-rhamnose 1-epimerase
controlled: Transport57563
control type: ACTIVATION

Dihydroxyacetone phosphate
type: SmallMolecule
cellular location: Cytosol
entity reference: Dihydroxyacetone phosphate
name: SubPathwayInput

Water
type: SmallMolecule
entity reference: Water

TransportCatalysis38498
type: Catalysis
controller: L-rhamnose 1-epimerase
controlled: Transport57562
control type: ACTIVATION

ReactionCatalysis851697
type: Catalysis
controller: L-rhamnose mutarotase
controlled: 5.1.3.32
control type: ACTIVATION

ReactionCatalysis851698
type: Catalysis
controller: L-rhamnose isomerase
controlled: 5.3.1.14
control type: ACTIVATION

ReactionCatalysis851699
type: Catalysis
controller: Rhamnulokinase
controlled: 2.7.1.5
control type: ACTIVATION

Compound/Generic40/Stoichiometry/1.0
type: Stoichiometry
physical entity: Reduced acceptor
stoichiometric coefficient: 1.0

Reference/ChEBI CHEBI 17617
type: UnificationXref
id: CHEBI:17617
db: ChEBI

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

Reference/SMPDB SMP0000930
type: UnificationXref
id: SMP0000930
db: SMPDB

Reference/ChEBI CHEBI 18041
type: UnificationXref
id: CHEBI:18041
db: ChEBI

Reference/ChemSpider 648
type: UnificationXref
id: 648
db: ChemSpider

ChemicalStructure/PW C001034
type: ChemicalStructure
structure format: SMILES

Reference/HMDB HMDB0001473
type: UnificationXref
id: HMDB0001473
db: HMDB

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

Reference/PubChem-compound 668
type: UnificationXref
id: 668
db: PubChem-compound

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

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

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

Reduced acceptor
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 15022

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

Reference/CAS 79-33-4
type: UnificationXref
id: 79-33-4
db: CAS

Compound/PW C001134/Stoichiometry/1.0
type: Stoichiometry
physical entity: Dihydroxyacetone phosphate
stoichiometric coefficient: 1.0

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

Reference/HMDB HMDB0124735
type: UnificationXref
id: HMDB0124735
db: HMDB

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/BioCyc DIHYDROXY-ACETONE-PHOSPHATE
type: UnificationXref
id: DIHYDROXY-ACETONE-PHOSPHATE
db: BioCyc

Reference/KEGG Compound C00186
type: UnificationXref
id: C00186
db: KEGG Compound

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

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

1.1.-.-
type: BiochemicalReaction
participant stoichiometry: Compound/Generic227/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000122/Stoichiometry/1.0
participant stoichiometry: Compound/Generic40/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000164/Stoichiometry/1.0
right: Reduced acceptor
right: Pyruvic acid
spontaneous: false
EC number: 1.1.-.-
left: L-Lactic acid
left: oxidized electron acceptor
name: L-Lactic acid + oxidized electron acceptor → Pyruvic acid + Reduced acceptor
conversion direction: LEFT_TO_RIGHT

4.1.2.17
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001134/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040962/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040963/Stoichiometry/1.0
right: Dihydroxyacetone phosphate
right: (S)-lactaldehyde
spontaneous: false
EC number: 4.1.2.17
left: L-fuculose 1-phosphate
name: L-fuculose 1-phosphate → (S)-lactaldehyde + Dihydroxyacetone phosphate
conversion direction: LEFT_TO_RIGHT

2.7.1.51
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000414/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040964/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040963/Stoichiometry/1.0
right: Adenosine diphosphate
right: L-fuculose 1-phosphate
right: Hydrogen Ion
spontaneous: false
EC number: 2.7.1.51
left: L-fuculose
left: Adenosine triphosphate
name: Adenosine triphosphate + L-fuculose → Adenosine diphosphate + Hydrogen Ion + L-fuculose 1-phosphate
conversion direction: LEFT_TO_RIGHT

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

5.3.1.25
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040965/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040964/Stoichiometry/1.0
right: L-fuculose
spontaneous: false
EC number: 5.3.1.25
left: α-L-fucopyranose
name: α-L-fucopyranose → L-fuculose
conversion direction: LEFT_TO_RIGHT

5.1.3.29
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040965/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040966/Stoichiometry/1.0
right: α-L-fucopyranose
spontaneous: false
EC number: 5.1.3.29
left: β-L-fucopyranose
name: β-L-fucopyranose → α-L-fucopyranose
conversion direction: LEFT_TO_RIGHT

1.1.1.77
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040967/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040962/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000721/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001144/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: NAD
right: (S)-Propane-1,2-diol
spontaneous: false
EC number: 1.1.1.77
left: NADH
left: (S)-lactaldehyde
left: Hydrogen Ion
name: (S)-lactaldehyde + Hydrogen Ion + NADH → (S)-Propane-1,2-diol + NAD
conversion direction: LEFT_TO_RIGHT

ChemicalStructure/PW C001134
type: ChemicalStructure
structure format: SMILES
structure data: OCC(=O)COP(O)(O)=O

Bacteroides intestinalis
type: BioSource
xref: Reference/TAXONOMY 329854

Reference/ChEBI CHEBI 42589
type: UnificationXref
id: CHEBI:42589
db: ChEBI

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

Compound/Generic227/Stoichiometry/1.0
type: Stoichiometry
physical entity: oxidized electron acceptor
stoichiometric coefficient: 1.0

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

Reference/ChEBI CHEBI 27907
type: UnificationXref
id: CHEBI:27907
db: ChEBI

2.7.1.5
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040960/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000414/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040961/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Adenosine diphosphate
right: L-rhamnulose 1-phosphate
right: Hydrogen Ion
spontaneous: false
EC number: 2.7.1.5
left: L-rhamnulofuranose
left: Adenosine triphosphate
name: Adenosine triphosphate + L-rhamnulofuranose → Adenosine diphosphate + Hydrogen Ion + L-rhamnulose 1-phosphate
conversion direction: LEFT_TO_RIGHT

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

4.1.2.19
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001134/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040962/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040961/Stoichiometry/1.0
right: Dihydroxyacetone phosphate
right: (S)-lactaldehyde
spontaneous: false
EC number: 4.1.2.19
left: L-rhamnulose 1-phosphate
name: L-rhamnulose 1-phosphate → (S)-lactaldehyde + Dihydroxyacetone phosphate
conversion direction: LEFT_TO_RIGHT

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

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

5.1.3.32
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040957/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040958/Stoichiometry/1.0
right: β-L-rhamnopyranose
spontaneous: false
EC number: 5.1.3.32
left: α-L-rhamnopyranose
name: α-L-rhamnopyranose → β-L-rhamnopyranose
conversion direction: LEFT_TO_RIGHT

5.3.1.14
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040959/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040958/Stoichiometry/1.0
right: keto-L-rhamnulose
spontaneous: false
EC number: 5.3.1.14
left: β-L-rhamnopyranose
name: β-L-rhamnopyranose → keto-L-rhamnulose
conversion direction: LEFT_TO_RIGHT

Compound/PW C040966/Stoichiometry/1.0
type: Stoichiometry
physical entity: β-L-fucopyranose
stoichiometric coefficient: 1.0

Protein/28065/Stoichiometry/2.0
type: Stoichiometry
physical entity: Unknown
stoichiometric coefficient: 2.0

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

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

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

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

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

L-1,2-propanediol oxidoreductase
type: Complex
component stoichiometry: Protein/31966/Stoichiometry/2.0
component: Lactaldehyde reductase

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

Reference/ChEBI CHEBI 16108
type: UnificationXref
id: CHEBI:16108
db: ChEBI

ChemicalStructure/PW C040958
type: ChemicalStructure
structure format: SMILES

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

ChemicalStructure/PW C040957
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C000414
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C040959
type: ChemicalStructure
structure format: SMILES
structure data: CC(O)C(O)C(O)C(=O)CO

Reference/ChEBI CHEBI 27586
type: UnificationXref
id: CHEBI:27586
db: ChEBI

Reference/ChEBI CHEBI 57846
type: UnificationXref
id: CHEBI:57846
db: ChEBI

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

Reference/UniProt B3CEI2
type: UnificationXref
id: B3CEI2
db: UniProt

Reference/ChEBI CHEBI 422
type: UnificationXref
id: CHEBI:422
db: ChEBI

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

L-Lactic acid
type: SmallMoleculeReference
xref: Reference/CAS 79-33-4
xref: Reference/ChEBI CHEBI 422
xref: Reference/HMDB HMDB0000190
xref: Reference/PubChem-compound 107689
xref: Reference/KEGG Compound C00186
xref: Reference/BioCyc L-LACTATE
xref: Reference/ChemSpider 96860
chemical formula: C3H6O3
molecular weight: 90.03169
structure: ChemicalStructure/PW C000122

Transport57563
type: Transport
participant stoichiometry: Compound/PW C040958 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034 Periplasmic Space/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040958 Periplasmic Space/Stoichiometry/1.0
right: Hydrogen Ion
right: β-L-rhamnopyranose
spontaneous: false
left: Hydrogen Ion
left: β-L-rhamnopyranose
name: Hydrogen Ion (→), β-L-rhamnopyranose (→) Transport: Bacteroides intestinalis, Periplasmic Space to Bacteroides intestinalis, Cytosol
conversion direction: LEFT_TO_RIGHT

Transport57562
type: Transport
participant stoichiometry: Compound/PW C040957 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034 Cytosol/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034 Periplasmic Space/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040957 Periplasmic Space/Stoichiometry/1.0
right: α-L-rhamnopyranose
right: Hydrogen Ion
spontaneous: false
left: α-L-rhamnopyranose
left: Hydrogen Ion
name: α-L-rhamnopyranose (→), Hydrogen Ion (→) Transport: Bacteroides intestinalis, Periplasmic Space to Bacteroides intestinalis, Cytosol
conversion direction: LEFT_TO_RIGHT

ChemicalStructure/PW C040961
type: ChemicalStructure
structure format: SMILES
structure data: CC(O)C(O)C(O)C(=C)COP(C)(O)=C

ChemicalStructure/PW C040960
type: ChemicalStructure
structure format: SMILES
structure data: CC1OC(O)(CO)C(O)C1O

ChemicalStructure/PW C040965
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C040964
type: ChemicalStructure
structure format: SMILES
structure data: CC(O)C(O)C(O)C(=O)CO

ChemicalStructure/PW C040963
type: ChemicalStructure
structure format: SMILES
structure data: CC(O)C(O)C(O)C(=O)COP([O-])([O-])=O

Reference/HMDB HMDB0000190
type: UnificationXref
id: HMDB0000190
db: HMDB

ChemicalStructure/PW C040962
type: ChemicalStructure
structure format: SMILES
structure data: CC(O)C=O

ChemicalStructure/PW C040967
type: ChemicalStructure
structure format: SMILES
structure data: CC(O)CO

ChemicalStructure/PW C040966
type: ChemicalStructure
structure format: SMILES
structure data: CC1OC(O)C(O)C(O)C1O

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

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

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

Reference/PathWhiz PW000913
type: UnificationXref
id: PW000913
db: PathWhiz

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

Compound/PW C040957 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: α-L-rhamnopyranose
stoichiometric coefficient: 1.0

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

Hydrogen Ion
type: SmallMolecule
cellular location: Periplasmic Space
entity reference: Hydrogen Ion

oxidized electron acceptor
type: SmallMoleculeReference

Reference/SMPDB SMP0411615
type: UnificationXref
id: SMP0411615
db: SMPDB

Protein/31966/Stoichiometry/2.0
type: Stoichiometry
physical entity: Lactaldehyde reductase
stoichiometric coefficient: 2.0

Compound/PW C040958 Cytosol/Stoichiometry/1.0
type: Stoichiometry
physical entity: β-L-rhamnopyranose
stoichiometric coefficient: 1.0

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

Protein/56325/Stoichiometry/4.0
type: Stoichiometry
physical entity: Putative rhamnulose-1-phosphate aldolase
stoichiometric coefficient: 4.0

β-L-rhamnopyranose
type: SmallMolecule
cellular location: Cytosol
entity reference: β-L-rhamnopyranose