Structure of PDB 2hdq Chain B Binding Site BS02
Receptor Information
>2hdq Chain B (length=358) Species:
83333
(Escherichia coli K-12) [
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APQQINDIVHRTITPLIEQQKIPGMAVAVIYQGKPYYFTWGYADIAKKQP
VTQQTLFELGSVSKTFTGVLGGDAIARGEIKLSDPTTKYWPELTAKQWNG
ITLLHLATYTAGGLPLQVPDEVKSSSDLLRFYQNWQPAWAPGTQRLYANS
SIGLFGALAVKPSGLSFEQAMQTRVFQPLKLNHTWINVPPAEEKNYAWGY
REGKAVHVSPGALDAEAYGVKSTIEDMARWVQSNLKPLDINEKTLQQGIQ
LAQSRYWQTGDMYQGLGWEMLDWPVNPDSIINGSDNKIALAARPVKAITP
PTPAVRASWVHKTGATGGFGSYVAFIPEKELGIVMLANKNYPNPARVDAA
WQILNALQ
Ligand information
Ligand ID
C21
InChI
InChI=1S/C5H4O2S/c6-5(7)4-2-1-3-8-4/h1-3H,(H,6,7)
InChIKey
QERYCTSHXKAMIS-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(sc1)C(=O)O
CACTVS 3.341
OC(=O)c1sccc1
ACDLabs 10.04
O=C(O)c1sccc1
Formula
C5 H4 O2 S
Name
THIOPHENE-2-CARBOXYLIC ACID
ChEMBL
CHEMBL1222314
DrugBank
ZINC
ZINC000000157468
PDB chain
2hdq Chain B Residue 505 [
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Receptor-Ligand Complex Structure
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PDB
2hdq
Deconstructing fragment-based inhibitor discovery
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
P140 W142 A143
Binding residue
(residue number reindexed from 1)
P137 W139 A140
Annotation score
1
Binding affinity
MOAD
: Ki=40mM
BindingDB: Ki=40000000nM
Enzymatic activity
Catalytic site (original residue number in PDB)
S64 K67 Y112 A114 V121 Y150 G156 E272 K315 A318
Catalytic site (residue number reindexed from 1)
S61 K64 Y109 A111 V118 Y147 G153 E269 K312 A315
Enzyme Commision number
3.5.2.6
: beta-lactamase.
Gene Ontology
Molecular Function
GO:0008800
beta-lactamase activity
GO:0016787
hydrolase activity
Biological Process
GO:0017001
antibiotic catabolic process
GO:0046677
response to antibiotic
Cellular Component
GO:0030288
outer membrane-bounded periplasmic space
GO:0042597
periplasmic space
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2hdq
,
PDBe:2hdq
,
PDBj:2hdq
PDBsum
2hdq
PubMed
17072304
UniProt
P00811
|AMPC_ECOLI Beta-lactamase (Gene Name=ampC)
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