Structure of PDB 2qf6 Chain C Binding Site BS01
Receptor Information
>2qf6 Chain C (length=207) Species:
9606
(Homo sapiens) [
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VETFAFQAEIAQLMSLIINTFYSNKEIFLRELISNSSDALDKIRYETLTD
PSKLDSGKELHINLIPNKQDRTLTIVDTGIGMTKADLINNLGTIAKSGTK
AFMEALQAGADISMIGQFGVGFYSAYLVAEKVTVITKHNDDEQYAWESSA
GGSFTVRTDTGEPMGRGTKVILHLKEDQTEYLEERRIKEIVKKHSQFIGY
PITLFVE
Ligand information
Ligand ID
A56
InChI
InChI=1S/C13H10BrN5/c14-10-6-8-4-2-1-3-7(8)5-9(10)11-17-12(15)19-13(16)18-11/h1-6H,(H4,15,16,17,18,19)
InChIKey
RXSSKAZHCZWJPP-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1ccc2cc(c(cc2c1)c3nc(nc(n3)N)N)Br
CACTVS 3.341
Nc1nc(N)nc(n1)c2cc3ccccc3cc2Br
ACDLabs 10.04
Brc3c(c1nc(nc(n1)N)N)cc2ccccc2c3
Formula
C13 H10 Br N5
Name
6-(3-BROMO-2-NAPHTHYL)-1,3,5-TRIAZINE-2,4-DIAMINE
ChEMBL
DrugBank
DB07319
ZINC
ZINC000036966120
PDB chain
2qf6 Chain C Residue 256 [
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Receptor-Ligand Complex Structure
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PDB
2qf6
Discovery and design of novel HSP90 inhibitors using multiple fragment-based design strategies.
Resolution
3.1 Å
Binding residue
(original residue number in PDB)
M98 N106 L107 F138 T184
Binding residue
(residue number reindexed from 1)
M82 N90 L91 F122 T168
Annotation score
1
Binding affinity
BindingDB: Ki=3.2e+2nM,Kd=<1.0e+4nM
Enzymatic activity
Enzyme Commision number
3.6.4.10
: non-chaperonin molecular chaperone ATPase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
GO:0051082
unfolded protein binding
GO:0140662
ATP-dependent protein folding chaperone
Biological Process
GO:0006457
protein folding
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Molecular Function
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Biological Process
External links
PDB
RCSB:2qf6
,
PDBe:2qf6
,
PDBj:2qf6
PDBsum
2qf6
PubMed
17630989
UniProt
P07900
|HS90A_HUMAN Heat shock protein HSP 90-alpha (Gene Name=HSP90AA1)
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