Structure of PDB 2wer Chain B Binding Site BS01
Receptor Information
>2wer Chain B (length=214) Species:
4932
(Saccharomyces cerevisiae) [
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MASETFEFQAEITQLMSLIINTVYSNKEIFLREIVSNASDALDKIRYKSL
SDPKQLETEPDLFIRITPKPEQKVLEIRDSGIGMTKAELINNLGTIAKSG
TKAFMEALSAGADVSMIGQFGVGFYSLFLVADRVQVISKSNDDEQYIWES
NAGGSFTVTLDEVNERIGRGTILRLFLKDDQLEYLEEKRIKEVIKRHSEF
VAYPIQLVVTKEVE
Ligand information
Ligand ID
RDC
InChI
InChI=1S/C18H17ClO6/c1-9-6-15-14(25-15)5-3-2-4-10(20)7-11-16(18(23)24-9)12(21)8-13(22)17(11)19/h2-5,8-9,14-15,21-22H,6-7H2,1H3/b4-2+,5-3-/t9-,14-,15-/m1/s1
InChIKey
WYZWZEOGROVVHK-GTMNPGAYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC1CC2C(O2)C=CC=CC(=O)Cc3c(c(cc(c3Cl)O)O)C(=O)O1
OpenEye OEToolkits 1.5.0
C[C@@H]1C[C@@H]2[C@H](O2)\C=C/C=C/C(=O)Cc3c(c(cc(c3Cl)O)O)C(=O)O1
CACTVS 3.341
C[C@@H]1C[C@H]2O[C@@H]2\C=C/C=C/C(=O)Cc3c(Cl)c(O)cc(O)c3C(=O)O1
ACDLabs 10.04
O=C2C=CC=CC3OC3CC(OC(=O)c1c(O)cc(O)c(Cl)c1C2)C
CACTVS 3.341
C[CH]1C[CH]2O[CH]2C=CC=CC(=O)Cc3c(Cl)c(O)cc(O)c3C(=O)O1
Formula
C18 H17 Cl O6
Name
RADICICOL;
MONORDEN
ChEMBL
CHEMBL414883
DrugBank
DB03758
ZINC
ZINC000013521629
PDB chain
2wer Chain B Residue 1215 [
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Receptor-Ligand Complex Structure
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PDB
2wer
Structural Basis of the Radicicol Resistance Displayed by a Fungal Hsp90.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
N37 D40 A41 K44 D79 I82 M84 F124 L173
Binding residue
(residue number reindexed from 1)
N37 D40 A41 K44 D79 I82 M84 F124 L173
Annotation score
1
Binding affinity
MOAD
: Kd=90nM
BindingDB: IC50=2e+2nM
Enzymatic activity
Enzyme Commision number
?
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
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2wer
,
PDBe:2wer
,
PDBj:2wer
PDBsum
2wer
PubMed
19236053
UniProt
P02829
|HSP82_YEAST ATP-dependent molecular chaperone HSP82 (Gene Name=HSP82)
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