Structure of PDB 5y6e Chain B Binding Site BS02
Receptor Information
>5y6e Chain B (length=231) Species:
287
(Pseudomonas aeruginosa) [
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EYPTVSEIPVGEVRLYQIADGVWSHIATQSFDGAVYPSNGLIVRDGDELL
LIDTAWGAKNTAALLAEIEKQIGLPVTRAVSTHFHDDRVGGVDVLRAAGV
ATYASPSTRRLAEVEGNEIPTHSLEGLSSSGDAVRFGPVELFYPGAAHST
DNLVVYVPSASVLYGGCAIYELSRTSAGNVADADLAEWPTSIERIQQHYP
EAQFVIPGHGLPGGLDLLKHTTNVVKAHTNR
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
5y6e Chain B Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
5y6e
((S)-3-Mercapto-2-methylpropanamido)acetic acid derivatives as metallo-beta-lactamase inhibitors: Synthesis, kinetic and crystallographic studies.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
D118 C198 H240
Binding residue
(residue number reindexed from 1)
D87 C167 H209
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H114 H116 D118 H179 C198 Y201 N210 H240
Catalytic site (residue number reindexed from 1)
H83 H85 D87 H148 C167 Y170 N179 H209
Enzyme Commision number
3.5.2.6
: beta-lactamase.
Gene Ontology
Molecular Function
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
Biological Process
GO:0017001
antibiotic catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:5y6e
,
PDBe:5y6e
,
PDBj:5y6e
PDBsum
5y6e
PubMed
29353720
UniProt
Q9K2N0
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