Structure of PDB 6h23 Chain N Binding Site BS01
Receptor Information
>6h23 Chain N (length=168) Species:
9606
(Homo sapiens) [
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YDIYSRLLRERIVCVMGPIDDSVASLVIAQLLFLQSESNKKPIHMAINSP
GGVVTAGLAIYDTMQYILNPICTWCVGQAASMGSLLLAAGTPGMRHSLPN
SRIMIHQPSIAIQAEEIMKLKKQLYNIYAKHTKQSLQVIESAMERDRYMS
PMEAQEFGILDKVLVHPP
Ligand information
Ligand ID
FJT
InChI
InChI=1S/C18H13ClFN3O4/c19-13-7-12(20)3-2-11(13)6-16-22-23-18(27-16)17(24)21-8-10-1-4-14-15(5-10)26-9-25-14/h1-5,7H,6,8-9H2,(H,21,24)
InChIKey
DDGOMXRMDQDHAN-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
Fc1ccc(Cc2oc(nn2)C(=O)NCc3ccc4OCOc4c3)c(Cl)c1
OpenEye OEToolkits 2.0.6
c1cc2c(cc1CNC(=O)c3nnc(o3)Cc4ccc(cc4Cl)F)OCO2
Formula
C18 H13 Cl F N3 O4
Name
~{N}-(1,3-benzodioxol-5-ylmethyl)-5-[(2-chloranyl-4-fluoranyl-phenyl)methyl]-1,3,4-oxadiazole-2-carboxamide
ChEMBL
DrugBank
ZINC
ZINC000013364070
PDB chain
6h23 Chain H Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
6h23
Selective Activation of Human Caseinolytic Protease P (ClpP).
Resolution
3.089 Å
Binding residue
(original residue number in PDB)
L104 F105 S108 Y138
Binding residue
(residue number reindexed from 1)
L32 F33 S36 Y66
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.4.21.92
: endopeptidase Clp.
Gene Ontology
Molecular Function
GO:0004176
ATP-dependent peptidase activity
GO:0004252
serine-type endopeptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:6h23
,
PDBe:6h23
,
PDBj:6h23
PDBsum
6h23
PubMed
30129683
UniProt
Q16740
|CLPP_HUMAN ATP-dependent Clp protease proteolytic subunit, mitochondrial (Gene Name=CLPP)
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