Structure of PDB 5o1g Chain A Binding Site BS02
Receptor Information
>5o1g Chain A (length=196) Species:
9606
(Homo sapiens) [
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SVPSQKTYQGSYGFRLGFLHSGTAKSVTCTYSPALNKLFCQLAKTCPVQL
WVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLI
RVEGNLRAEYLDDRNTFRHSVVVPCEPPEVGSDCTTIHYNYMCYSSCMGG
MNRRPILTIITLEDSSGNLLGRDSFEVRVCACPGRDRRTEEENLRK
Ligand information
Ligand ID
9GK
InChI
InChI=1S/C19H16INO4/c20-16-17(21-9-4-5-10-21)15(12-14(18(16)22)19(23)24)25-11-8-13-6-2-1-3-7-13/h1-7,9-10,12,22H,8,11H2,(H,23,24)
InChIKey
SLRGCKWWQXFSSN-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.6
c1ccc(cc1)CCOc2cc(c(c(c2n3cccc3)I)O)C(=O)O
CACTVS 3.385
OC(=O)c1cc(OCCc2ccccc2)c(n3cccc3)c(I)c1O
Formula
C19 H16 I N O4
Name
3-iodanyl-2-oxidanyl-5-(2-phenylethoxy)-4-pyrrol-1-yl-benzoic acid
ChEMBL
CHEMBL4171798
DrugBank
ZINC
PDB chain
5o1g Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
5o1g
Aminobenzothiazole derivatives stabilize the thermolabile p53 cancer mutant Y220C and show anticancer activity in p53-Y220C cell lines.
Resolution
1.35 Å
Binding residue
(original residue number in PDB)
L145 V147 T150 P151 P153 V157 C220 E221 P223 T230
Binding residue
(residue number reindexed from 1)
L50 V52 T55 P56 P58 V62 C125 E126 P128 T135
Annotation score
1
Binding affinity
MOAD
: Kd=116uM
PDBbind-CN
: -logKd/Ki=3.94,Kd=116uM
BindingDB: Kd=116000nM
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:5o1g
,
PDBe:5o1g
,
PDBj:5o1g
PDBsum
5o1g
PubMed
29702446
UniProt
P04637
|P53_HUMAN Cellular tumor antigen p53 (Gene Name=TP53)
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