Structure of PDB 5v8r Chain A Binding Site BS02
Receptor Information
>5v8r Chain A (length=402) Species:
1491
(Clostridium botulinum) [
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HHSSGLVPRGSHMQFVNKQFNYKDPVNGVDIAYIKIPNQMQPVKAFKIHN
KIWVIPERDTFTNPEEGDLNPPPVSYYDSTYLSTDNEKDNYLKGVTKLFE
RIYSTDLGRMLLTSIVRGIPFWGGSTIDTELKVIDTNCINVIQPDGSYRS
EELNLVIIGPSADIIQFECKSFGHEVLNLTRNGYGSTQYIRFSPDFTFGF
EESLEPLLGAGKFATDPAVTLAHELIHAGHRLYGIAINPNRVFKVSFEEL
RTFGGHDAKFIDSLQENEFRLYYYNKFKDIASTLNKAKSIVGASLQYMKN
VFKEKYLLSEDTSGKFSVDKLKFDKLYKMLTEIYTEDNFVKFFKVLNRKT
YLNDKAVFKINIVPKVNYTIYDGFNLRNTNLAANFNGQNTEINNMNFTKL
KN
Ligand information
Ligand ID
90J
InChI
InChI=1S/C11H10FN3OS/c12-8-3-1-7(2-4-8)9-5-13-15-11(9)14-10(16)6-17/h1-5,17H,6H2,(H2,13,14,15,16)
InChIKey
HWWIANSIKWTQRY-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
Fc1ccc(cc1)c2c[nH]nc2NC(=O)CS
ACDLabs 12.01
c2c(c1ccc(F)cc1)c(nn2)NC(=O)CS
OpenEye OEToolkits 2.0.6
c1cc(ccc1c2c[nH]nc2NC(=O)CS)F
Formula
C11 H10 F N3 O S
Name
N-[4-(4-fluorophenyl)-1H-pyrazol-3-yl]-2-sulfanylacetamide
ChEMBL
DrugBank
ZINC
PDB chain
5v8r Chain A Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
5v8r
Small molecule metalloprotease inhibitor with in vitro, ex vivo and in vivo efficacy against botulinum neurotoxin serotype A.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
I161 Q162 F163 F194 T220 H223 E224 E262 R363 Y366
Binding residue
(residue number reindexed from 1)
I165 Q166 F167 F198 T220 H223 E224 E249 R348 Y351
Annotation score
1
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 R348
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
View graph for
Biological Process
External links
PDB
RCSB:5v8r
,
PDBe:5v8r
,
PDBj:5v8r
PDBsum
5v8r
PubMed
28698055
UniProt
P0DPI1
|BXA1_CLOBH Botulinum neurotoxin type A (Gene Name=botA)
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