Structure of PDB 5o1h Chain A Binding Site BS02
Receptor Information
>5o1h Chain A (length=196) Species:
9606
(Homo sapiens) [
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SVPSQKTYQGSYGFRLGFLHSGTAKSVTCTYSPALNKLFCQLAKTCPVQL
WVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLI
RVEGNLRAEYLDDRNTFRHSVVVPCEPPEVGSDCTTIHYNYMCYSSCMGG
MNRRPILTIITLEDSSGNLLGRDSFEVRVCACPGRDRRTEEENLRK
Ligand information
Ligand ID
9GN
InChI
InChI=1S/C14H14INO3S/c1-2-7-20-10-8-9(14(18)19)13(17)11(15)12(10)16-5-3-4-6-16/h3-6,8,17H,2,7H2,1H3,(H,18,19)
InChIKey
IUCGBTPKFYQLQH-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.6
CCCSc1cc(c(c(c1n2cccc2)I)O)C(=O)O
CACTVS 3.385
CCCSc1cc(C(O)=O)c(O)c(I)c1n2cccc2
Formula
C14 H14 I N O3 S
Name
3-iodanyl-2-oxidanyl-5-propylsulfanyl-4-pyrrol-1-yl-benzoic acid
ChEMBL
CHEMBL4168439
DrugBank
ZINC
PDB chain
5o1h Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
5o1h
Aminobenzothiazole derivatives stabilize the thermolabile p53 cancer mutant Y220C and show anticancer activity in p53-Y220C cell lines.
Resolution
1.32 Å
Binding residue
(original residue number in PDB)
L145 V147 T150 P151 C220 P223 T230
Binding residue
(residue number reindexed from 1)
L50 V52 T55 P56 C125 P128 T135
Annotation score
1
Binding affinity
MOAD
: Kd=14uM
PDBbind-CN
: -logKd/Ki=4.85,Kd=14uM
BindingDB: Kd=14000nM
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000976
transcription cis-regulatory region binding
GO:0003677
DNA binding
GO:0003700
DNA-binding transcription factor activity
Biological Process
GO:0006355
regulation of DNA-templated transcription
GO:0006915
apoptotic process
Cellular Component
GO:0005634
nucleus
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5o1h
,
PDBe:5o1h
,
PDBj:5o1h
PDBsum
5o1h
PubMed
29702446
UniProt
P04637
|P53_HUMAN Cellular tumor antigen p53 (Gene Name=TP53)
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