Structure of PDB 5ew0 Chain B Binding Site BS01
Receptor Information
>5ew0 Chain B (length=228) Species:
47917
(Serratia fonticola) [
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NLTLTHFKGPLYIVEDKEYVQENSMVYIGTDGITIIGATWTPETAETLYK
EIRKVSPLPINEVINTNYHTDRAGGNAYWKTLGAKIVATQMTYDLQKSQW
GSIVNFTRQGNNKYPNLEKSLPDTVFPGDFNLQNGSIRAMYLGEAHTKDG
IFVYFPAERVLYGNCILKENLGNMSFANRTEYPKTLEKLKGLIEQGELKV
DSIIAGHDTPIHDVGLIDHYLTLLEKAP
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
5ew0 Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5ew0
Cross-class metallo-beta-lactamase inhibition by bisthiazolidines reveals multiple binding modes.
Resolution
1.3 Å
Binding residue
(original residue number in PDB)
D111 C205 H247
Binding residue
(residue number reindexed from 1)
D71 C165 H207
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
N107 H109 D111 H186 C205 K208 N213 H247
Catalytic site (residue number reindexed from 1)
N67 H69 D71 H146 C165 K168 N173 H207
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:5ew0
,
PDBe:5ew0
,
PDBj:5ew0
PDBsum
5ew0
PubMed
27303030
UniProt
Q9RMI1
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