Structure of PDB 5v8p Chain B Binding Site BS02
Receptor Information
>5v8p Chain B (length=402) Species:
1491
(Clostridium botulinum) [
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SSGLVPRGSHMQFVNKQFNYKDPVNGVDIAYIKIPQMQPVKAFKIHNKIW
VIPERDTFTNPEEGDLNPPVSYYDSTYLSTDNEKDNYLKGVTKLFERIYS
TDLGRMLLTSIVRGIPFWGGSTIDTELKVIDTNCINVIQPDGSYRSEELN
LVIIGPSADIIQFECKSFGHEVLNLTRNGYGSTQYIRFSPDFTFGFEESL
EVDTNPLLGAGKFATDPAVTLAHELIHAGHRLYGIAINPNRVFEVSFEEL
RTFGGHDAKFIDSLQENEFRLYYYNKFKDIASTLNKAKSIVGTASLQYMK
NVFKEKYLLSEDTSGKFSVDKLKFDKLYKMLTEIYTEDNFVKFFKVLNRK
TYLNFDKAVFKINIVPKVNYTIYDGFNLRNTNLAANFNGQNTEINNMNFT
KL
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
5v8p Chain B Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
5v8p
Small molecule metalloprotease inhibitor with in vitro, ex vivo and in vivo efficacy against botulinum neurotoxin serotype A.
Resolution
2.501 Å
Binding residue
(original residue number in PDB)
H223 H227 E262
Binding residue
(residue number reindexed from 1)
H223 H227 E249
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H223 E224 H227 E262 R363
Catalytic site (residue number reindexed from 1)
H223 E224 H227 E249 R349
Enzyme Commision number
3.4.24.69
: bontoxilysin.
Gene Ontology
Molecular Function
GO:0004222
metalloendopeptidase activity
GO:0008270
zinc ion binding
Biological Process
GO:0006508
proteolysis
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:5v8p
,
PDBe:5v8p
,
PDBj:5v8p
PDBsum
5v8p
PubMed
28698055
UniProt
P0DPI1
|BXA1_CLOBH Botulinum neurotoxin type A (Gene Name=botA)
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