Structure of PDB 4h5n Chain A Binding Site BS06
Receptor Information
>4h5n Chain A (length=382) Species:
9606
(Homo sapiens) [
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KGPAVGIDLGTTYSCVGVFQHGKVEIIANDQGNRTTPSYVAFTDTERLIG
DAAKNQVAMNPTNTVFDAKRLIGRRFDDAVVQSDMKHWPFMVVNDAGRPK
VQVEYKGETKSFYPEEVSSMVLTKMKEIAEAYLGKTVTNAVVTVPAYFND
SQRQATKDAGTIAGLNVLRIINEPTAAAIAYGLDKKVGAERNVLIFDLGG
GTFDVSILTIEDGIFEVKSTAGDTHLGGEDFDNRMVNHFIAEFKRKHKKD
ISENKRAVRRLRTACERAKRTLSSSTQASIEIDSLYEGIDFYTSITRARF
EELNADLFRGTLDPVEKALRDAKLDKSQIHDIVLVGGSTRIPKIQKLLQD
FFNGKELNKSINPDEAVAYGAAVQAAILSGDK
Ligand information
Ligand ID
GOL
InChI
InChI=1S/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2
InChIKey
PEDCQBHIVMGVHV-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
C(C(CO)O)O
ACDLabs 12.01
CACTVS 3.370
OCC(O)CO
Formula
C3 H8 O3
Name
GLYCEROL;
GLYCERIN;
PROPANE-1,2,3-TRIOL
ChEMBL
CHEMBL692
DrugBank
DB09462
ZINC
ZINC000000895048
PDB chain
4h5n Chain A Residue 408 [
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Receptor-Ligand Complex Structure
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PDB
4h5n
New crystal structures of HSC-70 ATP binding domain confirm the role of individual binding pockets and suggest a new method of inhibition.
Resolution
1.86 Å
Binding residue
(original residue number in PDB)
R272 S275 G339 R342
Binding residue
(residue number reindexed from 1)
R270 S273 G337 R340
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D10 K71 E175 D199
Catalytic site (residue number reindexed from 1)
D8 K69 E173 D197
Enzyme Commision number
3.6.4.10
: non-chaperonin molecular chaperone ATPase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0140662
ATP-dependent protein folding chaperone
View graph for
Molecular Function
External links
PDB
RCSB:4h5n
,
PDBe:4h5n
,
PDBj:4h5n
PDBsum
4h5n
PubMed
25433210
UniProt
P11142
|HSP7C_HUMAN Heat shock cognate 71 kDa protein (Gene Name=HSPA8)
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