Structure of PDB 5g4o Chain A Binding Site BS02
Receptor Information
>5g4o Chain A (length=196) Species:
9606
(Homo sapiens) [
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SVPSQKTYQGSYGFRLGFLHSGTAKSVTCTYSPALNKLFCQLAKTCPVQL
WVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLI
RVEGNLRAEYLDDRNTFRHSVVVPCEPPEVGSDCTTIHYNYMCYSSCMGG
MNRRPILTIITLEDSSGNLLGRDSFEVRVCACPGRDRRTEEENLRK
Ligand information
Ligand ID
O80
InChI
InChI=1S/C17H17F3N2/c1-21(2)10-12-7-8-16-14(9-12)13-5-3-4-6-15(13)22(16)11-17(18,19)20/h3-9H,10-11H2,1-2H3
InChIKey
FRGFVBVPVDCZLO-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
CN(C)Cc1ccc2c(c1)c3ccccc3n2CC(F)(F)F
CACTVS 3.385
CN(C)Cc1ccc2n(CC(F)(F)F)c3ccccc3c2c1
ACDLabs 12.01
c12n(c3c(c1cccc2)cc(cc3)CN(C)C)CC(F)(F)F
Formula
C17 H17 F3 N2
Name
N,N-dimethyl-1-[9-(2,2,2-trifluoroethyl)-9H-carbazol-3-yl]methanamine
ChEMBL
DrugBank
ZINC
ZINC000584905634
PDB chain
5g4o Chain A Residue 1293 [
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Receptor-Ligand Complex Structure
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PDB
5g4o
Harnessing Fluorine-Sulfur Contacts and Multipolar Interactions for the Design of P53 Mutant Y220C Rescue Drugs.
Resolution
1.48 Å
Binding residue
(original residue number in PDB)
L145 V147 T150 C220 E221 P222 P223 D228 T230
Binding residue
(residue number reindexed from 1)
L50 V52 T55 C125 E126 P127 P128 D133 T135
Annotation score
1
Binding affinity
MOAD
: Kd=37.2uM
PDBbind-CN
: -logKd/Ki=4.43,Kd=37uM
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:5g4o
,
PDBe:5g4o
,
PDBj:5g4o
PDBsum
5g4o
PubMed
27267810
UniProt
P04637
|P53_HUMAN Cellular tumor antigen p53 (Gene Name=TP53)
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