Structure of PDB 2fhx Chain B Binding Site BS02
Receptor Information
>2fhx Chain B (length=245) Species:
287
(Pseudomonas aeruginosa) [
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DHVDLPYNLTATKIDSDVFVVTDRDFYSSNVLVAKMLDGTVVIVSSPFEN
LGTQTLMDWVAKTMKPKKVVAINTHFHLDGTGGNEIYKKMGAETWSSDLT
KQLRLEENKKDRIKAAEFYKNEDLKRRILSSHPVPADNVFDLKQGKVFSF
SNELVEVSFPGPAHSPDNVVVYFPKKKLLFGGCMIKPKELGYLGDANVKA
WPDSARRLKKFDAKIVIPGHGEWGGPEMVNKTIKVAEKAVGEMRL
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
2fhx Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
2fhx
Crystal Structure of Pseudomonas aeruginosa SPM-1 Provides Insights into Variable Zinc Affinity of Metallo-beta-lactamases.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
H196 C221 K224 Y233
Binding residue
(residue number reindexed from 1)
H164 C183 K186 Y192
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H116 H118 D120 H196 C221 K224 Y233 H263
Catalytic site (residue number reindexed from 1)
H75 H77 D79 H164 C183 K186 Y192 H220
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:2fhx
,
PDBe:2fhx
,
PDBj:2fhx
PDBsum
2fhx
PubMed
16460758
UniProt
Q8G9Q0
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