Structure of PDB 2bg6 Chain B Binding Site BS01
Receptor Information
>2bg6 Chain B (length=218) Species:
1396
(Bacillus cereus) [
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KTVIKNETGTISISQLNKNVWVHTELGSAVPSNGLVLNTSKGLVLVDSSW
DDKLTKELIEMVEKKFQKRVTDVIITHAHADCIGGIKTLKERGIKAHSTA
LTAELAKKNGYEEPLGDLQTVTNLKFGNMKVETFYPGKGHTEDNIVVWLP
QYNILVGGCLVKSTSAKDLGNVADAYVNEWSTSIENVLKRYRNINAVVPG
HGEVGDKGLLLHTLDLLK
Ligand information
Ligand ID
AZI
InChI
InChI=1S/N3/c1-3-2/q-1
InChIKey
IVRMZWNICZWHMI-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[N-]=[N+]=[N-]
Formula
N3
Name
AZIDE ION
ChEMBL
CHEMBL79455
DrugBank
ZINC
PDB chain
2bg6 Chain B Residue 1299 [
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Receptor-Ligand Complex Structure
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PDB
2bg6
Effect of Ph on the Active Site of an Arg121Cys Mutant of the Metallo-Beta-Lactamase from Bacillus Cereus: Implications for the Enzyme Mechanism
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
H196 N233
Binding residue
(residue number reindexed from 1)
H140 N171
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H116 H118 D120 H196 C221 K224 N233 H263
Catalytic site (residue number reindexed from 1)
H77 H79 D81 H140 C159 K162 N171 H201
Enzyme Commision number
3.5.2.6
: beta-lactamase.
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0008800
beta-lactamase activity
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
Biological Process
GO:0017001
antibiotic catabolic process
GO:0046677
response to antibiotic
Cellular Component
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:2bg6
,
PDBe:2bg6
,
PDBj:2bg6
PDBsum
2bg6
PubMed
15779910
UniProt
P04190
|BLA2_BACCE Metallo-beta-lactamase type 2 (Gene Name=blm)
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