Structure of PDB 8gjh Chain A Binding Site BS01
Receptor Information
>8gjh Chain A (length=639) Species:
90371
(Salmonella enterica subsp. enterica serovar Typhimurium) [
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MKAVIFAYHDMGCQGVQAVLDAGYEIAAIFTHADGSVSRQAAELGIPVYA
PDNVNHPIWVDRIAELAPDIIFSFYYRNLLSEEILHLAPAGAFNLHGSLL
PAYRGRAPLNWVLVNGESETGVTLHRMVKRADAGEIVASQRVAIAQDDVA
LTLHHKLCQAARQLLNSILPTMKCGDIPSVPQRESDSTYYGRRRPEDGLI
DWHKPVSTVHNLVRAVAAPWPGAFSYNGSQKFTIWSSRMCPDAQGALPGS
VISVSPLRVACADGALEIITGQAGDDITVQGSQLAQTLGLVAGARLRRIR
VLILGVNGFIGNHLTERLLNEENYEVYGMDIGSNAISRFLLHPRFHFVEG
DISIHSEWIEYHVKKCDVVLPLVAIATPIEYTRNPLRVFELDFEENLRII
RYCVKYRKRVVFPSTSEVYGMCTDASFDEDKSNLIVGPVNKPRWIYSVSK
QLLDRVIWAYGEKEGLRFTLFRPFNWMGPRLDSLNAARIGSSRAITQLIL
NLVEGTPIKLIDGGQQKRCFTDIRDGIEALFRIIVNDGDRCDGKIINIGN
PDNEASIQELATLLLDSFDKHPLRCHFPPFAGFQVVESRSYYGKGYQDVA
HRKPSIDNARRCLGWEPSIAMRDTVEETLDFFLRSVDIA
Ligand information
Ligand ID
UGA
InChI
InChI=1S/C15H22N2O18P2/c18-5-1-2-17(15(26)16-5)12-9(22)6(19)4(32-12)3-31-36(27,28)35-37(29,30)34-14-10(23)7(20)8(21)11(33-14)13(24)25/h1-2,4,6-12,14,19-23H,3H2,(H,24,25)(H,27,28)(H,29,30)(H,16,18,26)/t4-,6-,7+,8+,9-,10-,11+,12-,14-/m1/s1
InChIKey
HDYANYHVCAPMJV-LXQIFKJMSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(O)C3OC(OP(=O)(O)OP(=O)(O)OCC2OC(N1C(=O)NC(=O)C=C1)C(O)C2O)C(O)C(O)C3O
CACTVS 3.341
O[CH]1[CH](O)[CH](O[CH]([CH]1O)C(O)=O)O[P](O)(=O)O[P](O)(=O)OC[CH]2O[CH]([CH](O)[CH]2O)N3C=CC(=O)NC3=O
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)(O)O[P@@](=O)(O)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)C(=O)O)O)O)O)O)O
CACTVS 3.341
O[C@@H]1[C@@H](O)[C@H](O[C@@H]([C@H]1O)C(O)=O)O[P@@](O)(=O)O[P@@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N3C=CC(=O)NC3=O
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OC3C(C(C(C(O3)C(=O)O)O)O)O)O)O
Formula
C15 H22 N2 O18 P2
Name
URIDINE-5'-DIPHOSPHATE-GLUCURONIC ACID;
UDP-GLUCURONIC ACID
ChEMBL
CHEMBL228057
DrugBank
DB03041
ZINC
ZINC000008215691
PDB chain
8gjh Chain A Residue 1100 [
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Receptor-Ligand Complex Structure
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PDB
8gjh
Targeting the Conformational Change in ArnA Dehydrogenase for Selective Inhibition of Polymyxin Resistance.
Resolution
3.6 Å
Binding residue
(original residue number in PDB)
A393 P395 Y398 S433 R460 N492 R510 A511 K526 I528 R535 I574 Y609 R619
Binding residue
(residue number reindexed from 1)
A376 P378 Y381 S416 R443 N475 R493 A494 K509 I511 R518 I557 Y592 R602
Annotation score
4
Enzymatic activity
Enzyme Commision number
1.1.1.305
: UDP-glucuronic acid oxidase (UDP-4-keto-hexauronic acid decarboxylating).
2.1.2.13
: UDP-4-amino-4-deoxy-L-arabinose formyltransferase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0016740
transferase activity
GO:0016742
hydroxymethyl-, formyl- and related transferase activity
GO:0016831
carboxy-lyase activity
GO:0099618
UDP-glucuronic acid dehydrogenase activity
GO:0099619
UDP-4-amino-4-deoxy-L-arabinose formyltransferase activity
Biological Process
GO:0009058
biosynthetic process
GO:0009103
lipopolysaccharide biosynthetic process
GO:0009245
lipid A biosynthetic process
GO:0046493
lipid A metabolic process
GO:0046677
response to antibiotic
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:8gjh
,
PDBe:8gjh
,
PDBj:8gjh
PDBsum
8gjh
PubMed
37410993
UniProt
O52325
|ARNA_SALTY Bifunctional polymyxin resistance protein ArnA (Gene Name=arnA)
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