Structure of PDB 3q7h Chain K Binding Site BS01
Receptor Information
>3q7h Chain K (length=189) Species:
360115
(Coxiella burnetii RSA 331) [
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VLVPMVVEQTRAYDIYSRLLKDRVIFLVGQVEDHMANLAIAQMLFLESEN
PNKDINLYINSPGGAVTSAMAIYDTMQFVKPDVRTLCIGQAASAGALLLA
GGAKGKRHCLPHSSVMIHQVLGGYQGQGTDIQIHAKQTQRVSDQLNQILA
KHTGKDIERVEKDTNRDYFLTPEEAVEYGLIDSIFKERP
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
3q7h Chain K Residue 198 [
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Receptor-Ligand Complex Structure
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PDB
3q7h
Structure of the ClpP subunit of the ATP-dependent Clp Protease from Coxiella burnetii
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
M82 V85 P87
Binding residue
(residue number reindexed from 1)
M76 V79 P81
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
G70 S99 A100 H124 D173
Catalytic site (residue number reindexed from 1)
G64 S93 A94 H118 D167
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
GO:0008236
serine-type peptidase activity
GO:0051117
ATPase binding
Biological Process
GO:0006508
proteolysis
GO:0006515
protein quality control for misfolded or incompletely synthesized proteins
Cellular Component
GO:0005737
cytoplasm
GO:0009368
endopeptidase Clp complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3q7h
,
PDBe:3q7h
,
PDBj:3q7h
PDBsum
3q7h
PubMed
UniProt
Q83DJ2
|CLPP_COXBU ATP-dependent Clp protease proteolytic subunit (Gene Name=clpP)
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