CHEBI:16015
ChEBI
2.0
30572
ChemSpider
C14H22N3O15P2
UDP-4-amino-4-deoxy-β-L-arabinopyranose
534.0526
C61H100NO8P
4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate
1005.7186
C15H23N3O16P2
UDP-4-deoxy-4-formamido-β-L-arabinopyranose
563.05536
937
ChemSpider
NADH
439153
PubChem-compound
SMILES
O
10-FORMYL-THF
BioCyc
50
ChemSpider
1.0
(KDO)2-lipid A
SMILES
O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]2OCC(=O)[C@H](O)[C@H]2O)O[C@H]([C@@H]1O)N1C=CC(=O)NC1=O
2616-64-0
CAS
UDP
NAD
CHEBI:58223
ChEBI
SMILES
NC1=NC(=O)C2=C(NC[C@H](CNC3=CC=C(C=C3)C(=O)NC(CCC(O)=O)C(O)=O)N2)N1
1.0
51
PubChem-compound
CHEBI:15846
ChEBI
C9H14N2O12P2
UDP
404.0022
C110H196N2O39P2
(KDO)2-lipid A
2231.2922
1.0
1038
PubChem-compound
CHEBI:17200
ChEBI
Undecaprenyl phosphate-alpha-4-amino-4-deoxy-L-arabinose arabinosyl transferase
278
ChemSpider
274
ChemSpider
C5H6O5
Oxoglutaric acid
146.02153
P77757
UniProt
1.0
Reaction5994
false
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
LEFT_TO_RIGHT
CHEBI:16908
ChEBI
2.4.2.43
false
2.4.2.43
(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
LEFT_TO_RIGHT
1.0
UDP-GLUCURONATE
BioCyc
SMILES
CCCCCCCCCCCCCC(=O)OC(CCCCCCCCCCC)CC(=O)OC1C(OP(O)(=O)OC2OCC(N)C(O)C2O)C(COC2(CC(OC3(CC(O)C(O)C(O3)C(O)CO)C(O)=O)C(O)C(O2)C(O)CO)C(O)=O)OC(OCC2OC(OP(O)(=O)OC3OCC(N)C(O)C3O)C(N=C(O)CC(O)CCCCCCCCCCC)C(OC(=O)CC(O)CCCCCCCCCCC)C2O)C1N=C(O)CC(CCCCCCCCCCC)OC(=O)CCCCCCCCCCC
1010
ChemSpider
ReactionCatalysis5956
ACTIVATION
1.0
C15H22N2O18P2
Uridine diphosphate glucuronic acid
580.0343
Hydrogen Ion
HMDB0000208
HMDB
Undecaprenyl-phosphate 4-deoxy-4-formamido-L-arabinose transferase
10-Formyltetrahydrofolate
SMILES
OC=N[C@@]1([H])CO[C@@]([H])(OP(O)(=O)OC\C([H])=C(\C)CC\C([H])=C(\C)CC\C([H])=C(\C)CC\C([H])=C(\C)CC\C([H])=C(\C)CC\C([H])=C(\C)CC\C([H])=C(\C)CC\C([H])=C(\C)CC\C([H])=C(/C)CC\C([H])=C(/C)CCC=C(C)C)[C@@](O)([H])[C@]1(O)[H]
C00234
KEGG Compound
CHEBI:47027
ChEBI
58-68-4
CAS
L-Glutamic acid
SMILES
OC(=O)CCC(=O)C(O)=O
122347
PubChem-compound
124-38-9
CAS
CHEBI:30915
ChEBI
CHEBI:15637
ChEBI
2.4.2.53
false
2.4.2.53
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
LEFT_TO_RIGHT
2.1.2.13
false
2.1.2.13
10-Formyltetrahydrofolate + UDP-4-amino-4-deoxy-β-L-arabinopyranose → Hydrogen Ion + Tetrahydrofolate + UDP-4-deoxy-4-formamido-β-L-arabinopyranose
LEFT_TO_RIGHT
Formic acid
2.6.1.87
false
2.6.1.87
L-Glutamic acid + UDP-β-L-threo-pentapyranos-4-ulose → Oxoglutaric acid + UDP-4-amino-4-deoxy-β-L-arabinopyranose
LEFT_TO_RIGHT
1.0
2.1.2.13
false
2.1.2.13
NAD + Uridine diphosphate glucuronic acid → Carbon dioxide + NADH + UDP-β-L-threo-pentapyranos-4-ulose
LEFT_TO_RIGHT
C120H220N4O45P2
L-Ara4N-modified KDO2-Lipid A
2499.4524
1.0
C00001
KEGG Compound
CHEBI:58540
ChEBI
SMILES
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
C00004
KEGG Compound
SMILES
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
C00003
KEGG Compound
17473
PubChem-compound
GLT
BioCyc
1.0
C21H28N7O14P2
NAD
664.11694
C00011
KEGG Compound
SMILES
O=C=O
1.0
HMDB0000902
HMDB
C21H29N7O14P2
NADH
665.12476
562
TAXONOMY
P77398
UniProt
H
Hydrogen Ion
1.007825
Undecaprenyl phosphate-alpha-4-amino-4-deoxy-L-arabinose arabinosyl transferase
53-84-9
CAS
UDP-4-deoxy-4-formamido-β-L-arabinopyranose
Uridine diphosphate glucuronic acid
C00026
KEGG Compound
UDP-4-amino-4-deoxy-β-L-arabinopyranose
C00025
KEGG Compound
4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate
SMILES
[H][C@@](O)(CCCCCCCCCCC)CC(=O)O[C@@]1([H])[C@]([H])(O)[C@@]([H])(CO[C@]2([H])O[C@]([H])(CO[C@@]3(C[C@@]([H])(O[C@@]4(C[C@@]([H])(O)[C@@]([H])(O)[C@]([H])(O4)[C@]([H])(O)CO)C([O-])=O)[C@@]([H])(O)[C@]([H])(O3)[C@]([H])(O)CO)C([O-])=O)[C@@]([H])(OP([O-])([O-])=O)[C@]([H])(OC(=O)C[C@@]([H])(CCCCCCCCCCC)OC(=O)CCCCCCCCCCCCC)[C@@]2([H])N=C([O-])C[C@@]([H])(CCCCCCCCCCC)OC(=O)CCCCCCCCCCC)O[C@]([H])(OP(O)(O)=O)[C@]1([H])N=C([O-])C[C@]([H])(O)CCCCCCCCCCC
UDP-β-L-threo-pentapyranos-4-ulose
SMILES
O[C@H]1[C@@H](O)[C@@H](O[C@@H]1COP(O)(=O)OP(O)(O)=O)N1C=CC(=O)NC1=O
1.0
1.0
SMILES
NC(=O)C1=C[N+](=CC=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O
C03541
KEGG Compound
5682
ChemSpider
Bifunctional polymyxin resistance protein ArnA
SMILES
NC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](CO[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C(N)N=CN=C23)[C@@H](O)[C@H]1O
328-50-7
CAS
1.0
Water
HMDB0000935
HMDB
C06026
KEGG Compound
C00167
KEGG Compound
1.0
HMDB0000148
HMDB
18971002
PubChem-compound
Polymyxin Resistance
HMDB0000142
HMDB
L-Ara4N-modified KDO2-Lipid A
2.0
Escherichia coli
388299
ChemSpider
7732-18-5
CAS
C00058
KEGG Compound
HMDB0001487
HMDB
CH2O2
Formic acid
46.005478
1.0
UDP-4-amino-4-deoxy-L-arabinose--oxoglutarate aminotransferase
56-86-0
CAS
FORMATE
BioCyc
16522
ChemSpider
C5H9NO4
L-Glutamic acid
147.05316
33032
PubChem-compound
CHEBI:16526
ChEBI
C14H20N2O16P2
UDP-β-L-threo-pentapyranos-4-ulose
534.0288
C20H23N7O7
10-Formyltetrahydrofolate
473.1659
PW002052
PathWhiz
1.0
1.0
2800-34-2
CAS
C19H23N7O6
Tetrahydrofolate
445.171
656478
PubChem-compound
Tetrahydrofolate
962
PubChem-compound
P77690
UniProt
2-KETOGLUTARATE
BioCyc
1.0
UDP-L-Ara4N formyltransferase / UDP-GlcA C-4"-decarboxylase
6.0
CO2
Carbon dioxide
43.98983
5893
PubChem-compound
di-trans,octa-cis-undecaprenyl diphosphate
di-trans,octa-cis-undecaprenyl phosphate
C00080
KEGG Compound
HMDB0000972
HMDB
CHEBI:30751
ChEBI
Oxoglutaric acid
SMILES
NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C=C3)C(=O)N[C@@H](CCC(O)=O)C(O)=O)N2)N1
SMILES
N[C@@H](CCC(O)=O)C(O)=O
HMDB0002111
HMDB
SMP0002065
SMPDB
SMILES
OC=O
CHEBI:15377
ChEBI
2.0
P76473
UniProt
CHEBI:15378
ChEBI
SMILES
[H+]
Bifunctional polymyxin resistance protein ArnA
4-Amino-4-deoxy-α-L-arabinopyranosyl di-trans,octa-cis-undecaprenyl phosphate
280
PubChem-compound
SMILES
[H][C@]1(COP(O)(=O)OP(O)(=O)O[C@@]2([H])OC[C@]([H])(N)[C@]([H])(O)[C@@]2([H])O)O[C@@]([H])(N2C=CC([O-])=NC2=O)[C@]([H])(O)[C@]1([H])O
SMILES
[H][C@]1(COP(O)(=O)OP(O)(=O)O[C@@]2([H])OC[C@]([H])(N=CO)[C@]([H])(O)[C@@]2([H])O)O[C@@]([H])(N2C=CC(O)=NC2=O)[C@]([H])(O)[C@]1([H])O
64-18-6
CAS
C61H100NO8P
4-Amino-4-deoxy-α-L-arabinopyranosyl di-trans,octa-cis-undecaprenyl phosphate
1005.7186
SMILES
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
SMILES
O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)O[C@H]([C@@H]1O)N1C=CC(=O)NC1=O
ReactionCatalysis3327
ACTIVATION
ReactionCatalysis3328
ACTIVATION
ReactionCatalysis3325
ACTIVATION
ReactionCatalysis3326
ACTIVATION
CHEBI:58708
ChEBI
H2O
Water
18.010565
CHEBI:47028
ChEBI
NADH
BioCyc
NAD
BioCyc
HMDB0059597
HMDB
109092
ChemSpider
Carbon dioxide
C55H92O7P2
di-trans,octa-cis-undecaprenyl diphosphate
926.63184
HMDB0001967
HMDB
Undecaprenyl-phosphate 4-deoxy-4-formamido-L-arabinose transferase
UDP-4-amino-4-deoxy-L-arabinose--oxoglutarate aminotransferase
C55H91O4P
di-trans,octa-cis-undecaprenyl phosphate
846.6655
1.0
CHEBI:53028
ChEBI
2.0