Structure of PDB 5fat Chain B Binding Site BS01
Receptor Information
>5fat Chain B (length=243) Species:
573
(Klebsiella pneumoniae) [
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KEWQENKSWNAHFTEHKSQGVVVLWNENKQQGFTNNLKRANQAFLPASTF
KIPNSLIALDLGVVKDEHQVFKWDGQTRDIATWNRDHNLITAMKYSVVPV
YQEFARQIGEARMSKMLHAFDYGNEDISGNVDSFWLDGGIRISATEQISF
LRKLYHNKLHVSERSQRIVKQAMLTEANGDYIIRAKTGYSTRIEPKIGWW
VGWVELDDNVWFFAMNMDMPTSDGLGLRQAITKEVLKQEKIIP
Ligand information
Ligand ID
CO
InChI
InChI=1S/Co/q+2
InChIKey
XLJKHNWPARRRJB-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Co+2]
CACTVS 3.341
[Co++]
Formula
Co
Name
COBALT (II) ION
ChEMBL
DrugBank
DB14205
ZINC
PDB chain
5fat Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5fat
Structural and Kinetic Characterization of Diazabicyclooctanes as Dual Inhibitors of Both Serine-beta-Lactamases and Penicillin-Binding Proteins.
Resolution
2.09 Å
Binding residue
(original residue number in PDB)
H34 E256
Binding residue
(residue number reindexed from 1)
H12 E234
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S70 K73 S118 Y123 W157 Y211
Catalytic site (residue number reindexed from 1)
S48 K51 S96 Y101 W135 Y189
Enzyme Commision number
3.5.2.6
: beta-lactamase.
Gene Ontology
Molecular Function
GO:0008658
penicillin 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
GO:0071555
cell wall organization
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Molecular Function
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Biological Process
External links
PDB
RCSB:5fat
,
PDBe:5fat
,
PDBj:5fat
PDBsum
5fat
PubMed
26731698
UniProt
Q6XEC0
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