Structure of PDB 2bfz Chain B Binding Site BS01
Receptor Information
>2bfz Chain B (length=218) Species:
1396
(Bacillus cereus) [
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KTVIKNETGTISISQLNKNVWVHTELGSAVPSNGLVLNTSKGLVLVDSSW
DDKLTKELIEMVEKKFQKRVTDVIITHAHADCIGGIKTLKERGIKAHSTA
LTAELAKKNGYEEPLGDLQTVTNLKFGNMKVETFYPGKGHTEDNIVVWLP
QYNILVGGCLVKSTSAKDLGNVADAYVNEWSTSIENVLKRYRNINAVVPG
HGEVGDKGLLLHTLDLLK
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
2bfz Chain B Residue 1297 [
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Receptor-Ligand Complex Structure
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PDB
2bfz
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)
H116 H118 H196
Binding residue
(residue number reindexed from 1)
H77 H79 H140
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:2bfz
,
PDBe:2bfz
,
PDBj:2bfz
PDBsum
2bfz
PubMed
15779910
UniProt
P04190
|BLA2_BACCE Metallo-beta-lactamase type 2 (Gene Name=blm)
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