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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 HMDB00148 HMDB 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 HMDB00142 HMDB 1.0 51 PubChem-compound CHEBI:15846 ChEBI HMDB00935 HMDB 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 HMDB59597 HMDB 274 ChemSpider C5H6O5 Oxoglutaric acid 146.02153 P77757 UniProt HMDB00902 HMDB 1.0 Reaction5994 false 2 4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate + 2 Water → 4-Amino-4-deoxy-alpha-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-alpha-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 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 HMDB00208 HMDB 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 → UDP + 4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate 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 C21H29N7O14P2 NADH 665.12476 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 polymyxin resistance C06026 KEGG Compound C00167 KEGG Compound 1.0 18971002 PubChem-compound L-Ara4N-modified KDO2-Lipid A 2.0 388299 ChemSpider 7732-18-5 CAS C00058 KEGG Compound CH2O2 Formic acid 46.005478 1.0 UDP-4-amino-4-deoxy-L-arabinose--oxoglutarate aminotransferase 56-86-0 CAS FORMATE BioCyc http://identifiers.org/smpdb/SMP02065 SMPDB 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 HMDB01967 HMDB 962 PubChem-compound HMDB00972 HMDB 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 HMDB02111 HMDB C00080 KEGG Compound 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 SMILES OC=O CHEBI:15377 ChEBI 2.0 P76473 UniProt CHEBI:15378 ChEBI SMILES [H+] Bifunctional polymyxin resistance protein ArnA 4-Amino-4-deoxy-alpha-L-arabinopyranosyl di-trans,octa-cis-undecaprenyl phosphate 280 PubChem-compound HMDB01487 HMDB 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-alpha-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 109092 ChemSpider Carbon dioxide C55H92O7P2 di-trans,octa-cis-undecaprenyl diphosphate 926.63184 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 Bifunctional polymyxin resistance protein ArnA UDP-4-amino- 4-deoxy-L- arabinose-- oxoglutarate aminotransferase Bifunctional polymyxin resistance protein ArnA Undecaprenyl- phosphate 4-deoxy-4- formamido-L- arabinose transferase Undecaprenyl phosphate- alpha-4- amino-4- deoxy-L- arabinose arabinosyl transferase Uridine diphosphate glucuronic acid NAD CO 2 NADH UDP-β-L- threo- pentapyranos- 4-ulose L-Glutamic acid Oxoglutaric acid UDP-4-amino- 4-deoxy-β-L- arabinopyranose 10- Formyltetrahydrofolate UDP-4-deoxy- 4-formamido- β-L- arabinopyranose H + Tetrahydrofolate di- trans,octa- cis- undecaprenyl phosphate UDP 4-deoxy-4- formamido-α- L- arabinopyranosyl ditrans,octacis- undecaprenyl phosphate H 2 O Formic acid 4-Amino-4- deoxy-alpha- L- arabinopyranosyl di- trans,octa- cis- undecaprenyl phosphate (KDO)2-lipid A di- trans,octa- cis- undecaprenyl diphosphate L-Ara4N- modified KDO2-Lipid A
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 HMDB00148 HMDB 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 HMDB00142 HMDB 1.0 51 PubChem-compound CHEBI:15846 ChEBI HMDB00935 HMDB 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 HMDB59597 HMDB 274 ChemSpider C5H6O5 Oxoglutaric acid 146.02153 P77757 UniProt HMDB00902 HMDB 1.0 Reaction5994 false 2 4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate + 2 Water → 4-Amino-4-deoxy-alpha-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-alpha-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 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 HMDB00208 HMDB 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 → UDP + 4-deoxy-4-formamido-α-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate 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 C21H29N7O14P2 NADH 665.12476 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 polymyxin resistance C06026 KEGG Compound C00167 KEGG Compound 1.0 18971002 PubChem-compound L-Ara4N-modified KDO2-Lipid A 2.0 388299 ChemSpider 7732-18-5 CAS C00058 KEGG Compound CH2O2 Formic acid 46.005478 1.0 UDP-4-amino-4-deoxy-L-arabinose--oxoglutarate aminotransferase 56-86-0 CAS FORMATE BioCyc http://identifiers.org/smpdb/SMP02065 SMPDB 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 HMDB01967 HMDB 962 PubChem-compound HMDB00972 HMDB 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 HMDB02111 HMDB C00080 KEGG Compound 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 SMILES OC=O CHEBI:15377 ChEBI 2.0 P76473 UniProt CHEBI:15378 ChEBI SMILES [H+] Bifunctional polymyxin resistance protein ArnA 4-Amino-4-deoxy-alpha-L-arabinopyranosyl di-trans,octa-cis-undecaprenyl phosphate 280 PubChem-compound HMDB01487 HMDB 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-alpha-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 109092 ChemSpider Carbon dioxide C55H92O7P2 di-trans,octa-cis-undecaprenyl diphosphate 926.63184 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 arnA arnB arnA arnC arnT Uridine diphosphate glucuronic acid NAD Carbon dioxide NADH UDP-β-L- threo- pentapyranos- 4-ulose L-Glutamic acid Oxoglutaric acid UDP-4-amino- 4-deoxy-β-L- arabinopyranose 10- Formyltetrahydrofolate UDP-4-deoxy- 4-formamido- β-L- arabinopyranose Hydrogen Ion Tetrahydrofolate di- trans,octa- cis- undecaprenyl phosphate UDP 4-deoxy-4- formamido-α- L- arabinopyranosyl ditrans,octacis- undecaprenyl phosphate Water Formic acid 4-Amino-4- deoxy-alpha- L- arabinopyranosyl di- trans,octa- cis- undecaprenyl phosphate (KDO)2-lipid A di- trans,octa- cis- undecaprenyl diphosphate L-Ara4N- modified KDO2-Lipid A