Structure of PDB 4phk Chain A Binding Site BS05
Receptor Information
>4phk Chain A (length=173) Species:
9606
(Homo sapiens) [
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EEVRQFRRLFAQLAGDDMEVSATELMNILNKVVTRHPDLKTDGFGIDTCR
SMVAVMDSDTTGKLGFEEFKYLWNNIKRWQAIYKQFDTDRSGTICSSELP
GAFEAAGFHLNEHLYNMIIRRYSDESGNMDFDNFISCLVRLDAMFRAFKS
LDKDGTGQIQVNIQEWLQLTMYS
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
4phk Chain A Residue 305 [
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Receptor-Ligand Complex Structure
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PDB
4phk
The structural basis of differential inhibition of human calpain by indole and phenyl alpha-mercaptoacrylic acids.
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
D137 D225 D227 N228
Binding residue
(residue number reindexed from 1)
D42 D130 D132 N133
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
F164 G187 I189
Catalytic site (residue number reindexed from 1)
F69 G92 I94
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005509
calcium ion binding
View graph for
Molecular Function
External links
PDB
RCSB:4phk
,
PDBe:4phk
,
PDBj:4phk
PDBsum
4phk
PubMed
25086406
UniProt
P04632
|CPNS1_HUMAN Calpain small subunit 1 (Gene Name=CAPNS1)
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