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

Compound/PW C042616/Stoichiometry/2.0
type: Stoichiometry
physical entity: di-trans,octa-cis-undecaprenyl diphosphate
stoichiometric coefficient: 2.0

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

UDP-4-amino-4-deoxy-β-L-arabinopyranose
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 58708
chemical formula: C14H22N3O15P2
molecular weight: 534.0526
structure: ChemicalStructure/PW C042900

4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 53028
chemical formula: C61H100NO8P
molecular weight: 1005.7186
structure: ChemicalStructure/PW C042902

UDP-4-deoxy-4-formamido-β-L-arabinopyranose
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 47027
chemical formula: C15H23N3O16P2
molecular weight: 563.05536
structure: ChemicalStructure/PW C042901

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

NADH
type: SmallMolecule
entity reference: NADH

Acinetobacter lwoffii WJ10621
type: BioSource
xref: Reference/TAXONOMY 1046625

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

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

Reference/BioCyc 10-FORMYL-THF
type: UnificationXref
id: 10-FORMYL-THF
db: BioCyc

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

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

Unknown
type: Protein
entity reference: Unknown

(KDO)2-lipid A
type: SmallMolecule
entity reference: (KDO)2-lipid A

ChemicalStructure/PW C042899
type: ChemicalStructure
structure format: SMILES

Reference/CAS 2616-64-0
type: UnificationXref
id: 2616-64-0
db: CAS

UDP
type: SmallMolecule
entity reference: UDP

NAD
type: SmallMolecule
entity reference: NAD

Reference/ChEBI CHEBI 58223
type: UnificationXref
id: CHEBI:58223
db: ChEBI

ChemicalStructure/PW C040918
type: ChemicalStructure
structure format: SMILES

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

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

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

UDP
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 58223
chemical formula: C9H14N2O12P2
molecular weight: 404.0022
structure: ChemicalStructure/PW C040980

(KDO)2-lipid A
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 58540
xref: Reference/KEGG Compound C06026
chemical formula: C110H196N2O39P2
molecular weight: 2231.2922
structure: ChemicalStructure/PW C040740

Compound/PW C042899/Stoichiometry/1.0
type: Stoichiometry
physical entity: UDP-β-L-threo-pentapyranos-4-ulose
stoichiometric coefficient: 1.0

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

Reference/ChEBI CHEBI 17200
type: UnificationXref
id: CHEBI:17200
db: ChEBI

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

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

Oxoglutaric acid
type: SmallMoleculeReference
xref: Reference/CAS 328-50-7
xref: Reference/PubChem-compound 51
xref: Reference/BioCyc 2-KETOGLUTARATE
xref: Reference/HMDB HMDB0000208
xref: Reference/ChEBI CHEBI 30915
xref: Reference/KEGG Compound C00026
xref: Reference/ChemSpider 50
chemical formula: C5H6O5
molecular weight: 146.02153
structure: ChemicalStructure/PW C000134

Compound/PW C042900/Stoichiometry/1.0
type: Stoichiometry
physical entity: UDP-4-amino-4-deoxy-β-L-arabinopyranose
stoichiometric coefficient: 1.0

Reaction5994
type: BiochemicalReaction
participant stoichiometry: Compound/PW C042902/Stoichiometry/2.0
participant stoichiometry: Compound/PW C000092/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001420/Stoichiometry/2.0
participant stoichiometry: Compound/PW C042606/Stoichiometry/1.0
right: Formic acid
right: 4-Amino-4-deoxy-α-L-arabinopyranosyl di-trans,octa-cis-undecaprenyl phosphate
spontaneous: false
left: Water
left: 4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate
name: 2 4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate + 2 Water → 4-Amino-4-deoxy-α-L-arabinopyranosyl di-trans,octa-cis-undecaprenyl phosphate + Formic acid
conversion direction: LEFT_TO_RIGHT

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

Compound/PW C042902/Stoichiometry/1.0
type: Stoichiometry
physical entity: 4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate
stoichiometric coefficient: 1.0

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

ChemicalStructure/PW C041467
type: ChemicalStructure
structure format: SMILES

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

Uridine diphosphate glucuronic acid
type: SmallMoleculeReference
xref: Reference/BioCyc UDP-GLUCURONATE
xref: Reference/CAS 2616-64-0
xref: Reference/PubChem-compound 17473
xref: Reference/HMDB HMDB0000935
xref: Reference/ChEBI CHEBI 17200
xref: Reference/ChemSpider 16522
xref: Reference/KEGG Compound C00167
chemical formula: C15H22N2O18P2
molecular weight: 580.0343
structure: ChemicalStructure/PW C000746

Hydrogen Ion
type: SmallMolecule
entity reference: Hydrogen Ion

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

10-Formyltetrahydrofolate
type: SmallMolecule
entity reference: 10-Formyltetrahydrofolate

ChemicalStructure/PW C042606
type: ChemicalStructure
structure format: SMILES

Reference/KEGG Compound C00234
type: UnificationXref
id: C00234
db: KEGG Compound

Reference/ChEBI CHEBI 47027
type: UnificationXref
id: CHEBI:47027
db: ChEBI

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

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

Protein/29267/Stoichiometry/6.0
type: Stoichiometry
physical entity: Unknown
stoichiometric coefficient: 6.0

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

Reference/PubChem-compound 122347
type: UnificationXref
id: 122347
db: PubChem-compound

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

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

Reference/ChEBI CHEBI 15637
type: UnificationXref
id: CHEBI:15637
db: ChEBI

Formic acid
type: SmallMolecule
entity reference: Formic acid

Compound/PW C040980/Stoichiometry/1.0
type: Stoichiometry
physical entity: UDP
stoichiometric coefficient: 1.0

L-Ara4N-modified KDO2-Lipid A
type: SmallMoleculeReference
xref: Reference/PubChem-compound 656478
chemical formula: C120H220N4O45P2
molecular weight: 2499.4524
structure: ChemicalStructure/PW C041467

Amino Sugar and Nucleotide Sugar Metabolism III
type: Pathway
pathway order: SubPathwayInteractionSteps/SubPathway527453
pathway component: SubPathwayInteraction527453
xref: Reference/SMPDB SMP0000914
xref: Reference/PathWhiz PW000895
name: SubPathway

Reference/PathWhiz PW000895
type: UnificationXref
id: PW000895
db: PathWhiz

Compound/PW C040740/Stoichiometry/1.0
type: Stoichiometry
physical entity: (KDO)2-lipid A
stoichiometric coefficient: 1.0

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

Reference/ChEBI CHEBI 58540
type: UnificationXref
id: CHEBI:58540
db: ChEBI

ChemicalStructure/PW C042616
type: ChemicalStructure
structure format: SMILES
structure data: CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/COP(O)(=O)OP(O)(O)=O

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

ChemicalStructure/PW C042617
type: ChemicalStructure
structure format: SMILES
structure data: CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/COP(O)(O)=O

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

2.1.2.13
type: BiochemicalReaction
participant stoichiometry: Compound/PW C040918/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000774/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042901/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042900/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
right: Tetrahydrofolate
right: Hydrogen Ion
right: UDP-4-deoxy-4-formamido-β-L-arabinopyranose
spontaneous: false
EC number: 2.1.2.13
left: 10-Formyltetrahydrofolate
left: UDP-4-amino-4-deoxy-β-L-arabinopyranose
name: 10-Formyltetrahydrofolate + UDP-4-amino-4-deoxy-β-L-arabinopyranose → Hydrogen Ion + Tetrahydrofolate + UDP-4-deoxy-4-formamido-β-L-arabinopyranose
conversion direction: LEFT_TO_RIGHT

Reference/PubChem-compound 17473
type: UnificationXref
id: 17473
db: PubChem-compound

2.6.1.87
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000095/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042899/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000134/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042900/Stoichiometry/1.0
right: Oxoglutaric acid
right: UDP-4-amino-4-deoxy-β-L-arabinopyranose
spontaneous: false
EC number: 2.6.1.87
left: UDP-β-L-threo-pentapyranos-4-ulose
left: L-Glutamic acid
name: L-Glutamic acid + UDP-β-L-threo-pentapyranos-4-ulose → Oxoglutaric acid + UDP-4-amino-4-deoxy-β-L-arabinopyranose
conversion direction: LEFT_TO_RIGHT

Reference/TAXONOMY 1046625
type: UnificationXref
id: 1046625
db: TAXONOMY

2.1.2.13
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000746/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001316/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000721/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042899/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001144/Stoichiometry/1.0
right: NADH
right: UDP-β-L-threo-pentapyranos-4-ulose
right: Carbon dioxide
spontaneous: false
EC number: 2.1.2.13
left: NAD
left: Uridine diphosphate glucuronic acid
name: NAD + Uridine diphosphate glucuronic acid → Carbon dioxide + NADH + UDP-β-L-threo-pentapyranos-4-ulose
conversion direction: LEFT_TO_RIGHT

Unknown
type: ProteinReference

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

Reference/SMPDB SMP0479566
type: UnificationXref
id: SMP0479566
db: SMPDB

Compound/PW C042617/Stoichiometry/1.0
type: Stoichiometry
physical entity: di-trans,octa-cis-undecaprenyl phosphate
stoichiometric coefficient: 1.0

2.4.2.53
type: BiochemicalReaction
participant stoichiometry: Compound/PW C042902/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042901/Stoichiometry/1.0
participant stoichiometry: Compound/PW C042617/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040980/Stoichiometry/1.0
right: UDP
right: 4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate
spontaneous: false
EC number: 2.4.2.53
left: UDP-4-deoxy-4-formamido-β-L-arabinopyranose
left: di-trans,octa-cis-undecaprenyl phosphate
name: UDP-4-deoxy-4-formamido-β-L-arabinopyranose + di-trans,octa-cis-undecaprenyl phosphate → 4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate + UDP
conversion direction: LEFT_TO_RIGHT

2.4.2.43
type: BiochemicalReaction
participant stoichiometry: Compound/PW C042616/Stoichiometry/2.0
participant stoichiometry: Compound/PW C042606/Stoichiometry/2.0
participant stoichiometry: Compound/PW C040740/Stoichiometry/1.0
participant stoichiometry: Compound/PW C041467/Stoichiometry/1.0
right: L-Ara4N-modified KDO2-Lipid A
right: di-trans,octa-cis-undecaprenyl diphosphate
spontaneous: false
EC number: 2.4.2.43
left: (KDO)2-lipid A
left: 4-Amino-4-deoxy-α-L-arabinopyranosyl di-trans,octa-cis-undecaprenyl phosphate
name: (KDO)2-lipid A + 2 4-Amino-4-deoxy-α-L-arabinopyranosyl di-trans,octa-cis-undecaprenyl phosphate → L-Ara4N-modified KDO2-Lipid A + 2 di-trans,octa-cis-undecaprenyl diphosphate
conversion direction: LEFT_TO_RIGHT

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

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

Compound/PW C042901/Stoichiometry/1.0
type: Stoichiometry
physical entity: UDP-4-deoxy-4-formamido-β-L-arabinopyranose
stoichiometric coefficient: 1.0

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

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

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

UDP-4-deoxy-4-formamido-β-L-arabinopyranose
type: SmallMolecule
entity reference: UDP-4-deoxy-4-formamido-β-L-arabinopyranose

Uridine diphosphate glucuronic acid
type: SmallMolecule
entity reference: Uridine diphosphate glucuronic acid
name: SubPathwayOutput

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

UDP-4-amino-4-deoxy-β-L-arabinopyranose
type: SmallMolecule
entity reference: UDP-4-amino-4-deoxy-β-L-arabinopyranose

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

4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate
type: SmallMolecule
entity reference: 4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate

ChemicalStructure/PW C040740
type: ChemicalStructure
structure format: SMILES

UDP-β-L-threo-pentapyranos-4-ulose
type: SmallMolecule
entity reference: UDP-β-L-threo-pentapyranos-4-ulose

ChemicalStructure/PW C040980
type: ChemicalStructure
structure format: SMILES

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

Compound/PW C000774/Stoichiometry/1.0
type: Stoichiometry
physical entity: 10-Formyltetrahydrofolate
stoichiometric coefficient: 1.0

ChemicalStructure/PW C000721
type: ChemicalStructure
structure format: SMILES

Reference/KEGG Compound C03541
type: UnificationXref
id: C03541
db: KEGG Compound

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

ChemicalStructure/PW C001144
type: ChemicalStructure
structure format: SMILES

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

Compound/PW C000746/Stoichiometry/1.0
type: Stoichiometry
physical entity: Uridine diphosphate glucuronic acid
stoichiometric coefficient: 1.0

Water
type: SmallMolecule
entity reference: Water

Reference/HMDB HMDB0000935
type: UnificationXref
id: HMDB0000935
db: HMDB

UDP-L-Ara4N formyltransferase / UDP-GlcA C-4"-decarboxylase
type: Complex
component stoichiometry: Protein/29267/Stoichiometry/6.0
component: Unknown

Reference/KEGG Compound C06026
type: UnificationXref
id: C06026
db: KEGG Compound

Reference/KEGG Compound C00167
type: UnificationXref
id: C00167
db: KEGG Compound

Compound/PW C040918/Stoichiometry/1.0
type: Stoichiometry
physical entity: Tetrahydrofolate
stoichiometric coefficient: 1.0

ReactionCatalysis1319768
type: Catalysis
controller: Unknown
controlled: 2.4.2.43
control type: ACTIVATION

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

ReactionCatalysis1319766
type: Catalysis
controller: Unknown
controlled: 2.4.2.53
control type: ACTIVATION

ReactionCatalysis1319764
type: Catalysis
controller: UDP-L-Ara4N formyltransferase / UDP-GlcA C-4"-decarboxylase
controlled: 2.1.2.13
control type: ACTIVATION

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

ReactionCatalysis1319760
type: Catalysis
controller: UDP-L-Ara4N formyltransferase / UDP-GlcA C-4"-decarboxylase
controlled: 2.1.2.13
control type: ACTIVATION

ReactionCatalysis1319761
type: Catalysis
controller: Unknown
controlled: 2.6.1.87
control type: ACTIVATION

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

L-Ara4N-modified KDO2-Lipid A
type: SmallMolecule
entity reference: L-Ara4N-modified KDO2-Lipid A

Compound/PW C042606/Stoichiometry/2.0
type: Stoichiometry
physical entity: 4-Amino-4-deoxy-α-L-arabinopyranosyl di-trans,octa-cis-undecaprenyl phosphate
stoichiometric coefficient: 2.0

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

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

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

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

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

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

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

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

Reference/ChemSpider 16522
type: UnificationXref
id: 16522
db: ChemSpider

L-Glutamic acid
type: SmallMoleculeReference
xref: Reference/PubChem-compound 33032
xref: Reference/ChEBI CHEBI 16015
xref: Reference/ChemSpider 30572
xref: Reference/HMDB HMDB0000148
xref: Reference/CAS 56-86-0
xref: Reference/BioCyc GLT
xref: Reference/KEGG Compound C00025
chemical formula: C5H9NO4
molecular weight: 147.05316
structure: ChemicalStructure/PW C000095

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

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

UDP-β-L-threo-pentapyranos-4-ulose
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 47028
chemical formula: C14H20N2O16P2
molecular weight: 534.0288
structure: ChemicalStructure/PW C042899

10-Formyltetrahydrofolate
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0000972
xref: Reference/PubChem-compound 122347
xref: Reference/ChemSpider 109092
xref: Reference/ChEBI CHEBI 15637
xref: Reference/CAS 2800-34-2
xref: Reference/BioCyc 10-FORMYL-THF
xref: Reference/KEGG Compound C00234
chemical formula: C20H23N7O7
molecular weight: 473.1659
structure: ChemicalStructure/PW C000774

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

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

Reference/CAS 2800-34-2
type: UnificationXref
id: 2800-34-2
db: CAS

Tetrahydrofolate
type: SmallMoleculeReference
xref: Reference/KEGG Compound C03541
chemical formula: C19H23N7O6
molecular weight: 445.171
structure: ChemicalStructure/PW C040918

Reference/PubChem-compound 656478
type: UnificationXref
id: 656478
db: PubChem-compound

Tetrahydrofolate
type: SmallMolecule
entity reference: Tetrahydrofolate

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

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

Compound/PW C042606/Stoichiometry/1.0
type: Stoichiometry
physical entity: 4-Amino-4-deoxy-α-L-arabinopyranosyl di-trans,octa-cis-undecaprenyl phosphate
stoichiometric coefficient: 1.0

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

di-trans,octa-cis-undecaprenyl diphosphate
type: SmallMolecule
entity reference: di-trans,octa-cis-undecaprenyl diphosphate

di-trans,octa-cis-undecaprenyl phosphate
type: SmallMolecule
entity reference: di-trans,octa-cis-undecaprenyl phosphate

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

Reference/HMDB HMDB0000972
type: UnificationXref
id: HMDB0000972
db: HMDB

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

Oxoglutaric acid
type: SmallMolecule
entity reference: Oxoglutaric acid

ChemicalStructure/PW C000774
type: ChemicalStructure
structure format: SMILES

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

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

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

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

Compound/PW C042902/Stoichiometry/2.0
type: Stoichiometry
physical entity: 4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate
stoichiometric coefficient: 2.0

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

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

4-Amino-4-deoxy-α-L-arabinopyranosyl di-trans,octa-cis-undecaprenyl phosphate
type: SmallMolecule
entity reference: 4-Amino-4-deoxy-α-L-arabinopyranosyl di-trans,octa-cis-undecaprenyl phosphate

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

ChemicalStructure/PW C042900
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C042901
type: ChemicalStructure
structure format: SMILES

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

4-Amino-4-deoxy-α-L-arabinopyranosyl di-trans,octa-cis-undecaprenyl phosphate
type: SmallMoleculeReference
chemical formula: C61H100NO8P
molecular weight: 1005.7186
structure: ChemicalStructure/PW C042606

ChemicalStructure/PW C042902
type: ChemicalStructure
structure format: SMILES
structure data: CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/CC\C(C)=C/COP(O)(=O)OC1OCC(NC=O)C(O)C1O

ChemicalStructure/PW C000746
type: ChemicalStructure
structure format: SMILES

Reference/PathWhiz PW501573
type: UnificationXref
id: PW501573
db: PathWhiz

Polymyxin Resistance
type: Pathway
pathway order: PathwayEnzymeReaction/7007450
pathway order: PathwaySubPathway/527453
pathway order: PathwayEnzymeReaction/7007452
pathway order: PathwayEnzymeReaction/7007453
pathway order: PathwayEnzymeReaction/7007445
pathway order: PathwayEnzymeReaction/7007456
pathway order: PathwayEnzymeReaction/7007446
pathway component: 2.1.2.13
pathway component: ReactionCatalysis1319768
pathway component: Amino Sugar and Nucleotide Sugar Metabolism III
pathway component: 2.6.1.87
pathway component: ReactionCatalysis1319766
pathway component: ReactionCatalysis1319764
pathway component: ReactionCatalysis1319760
pathway component: ReactionCatalysis1319761
pathway component: 2.4.2.53
pathway component: Reaction5994
pathway component: 2.4.2.43
xref: Reference/PathWhiz PW501573
xref: Reference/SMPDB SMP0479566
organism: Acinetobacter lwoffii WJ10621

Reference/ChEBI CHEBI 58708
type: UnificationXref
id: CHEBI:58708
db: ChEBI

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/ChEBI CHEBI 47028
type: UnificationXref
id: CHEBI:47028
db: ChEBI

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

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

Reference/SMPDB SMP0000914
type: UnificationXref
id: SMP0000914
db: SMPDB

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

Reference/ChemSpider 109092
type: UnificationXref
id: 109092
db: ChemSpider

Carbon dioxide
type: SmallMolecule
entity reference: Carbon dioxide

di-trans,octa-cis-undecaprenyl diphosphate
type: SmallMoleculeReference
chemical formula: C55H92O7P2
molecular weight: 926.63184
structure: ChemicalStructure/PW C042616

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

SubPathwayInteraction527453
type: Interaction
name: SubPathwayReaction
name: SubPathway527453Reaction
participant: Uridine diphosphate glucuronic acid

di-trans,octa-cis-undecaprenyl phosphate
type: SmallMoleculeReference
chemical formula: C55H91O4P
molecular weight: 846.6655
structure: ChemicalStructure/PW C042617

Compound/PW C041467/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Ara4N-modified KDO2-Lipid A
stoichiometric coefficient: 1.0

Reference/ChEBI CHEBI 53028
type: UnificationXref
id: CHEBI:53028
db: ChEBI

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