Structure of PDB 3k8s Chain B Binding Site BS02
Receptor Information
>3k8s Chain B (length=258) Species:
9606
(Homo sapiens) [
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ESADLRALAKHLYDSYIKSFPLTKAKARAILTGKTTDKSPFVIYDMNSLM
MGEDKKEVAIRIFQGCQFRSVEAVQEITEYAKSIPGFVNLDLNDQVTLLK
YGVHEIIYTMLASLMNKDGVLISEGQGFMTREFLKSLRKPFGDFMEPKFE
FAVKFNALELDDSDLAIFIAVIILSGDRPGLLNVKPIEDIQDNLLQALEL
QLKLNHPESSQLFAKLLQKMTDLRQIVTEHVQLLQVIKKTETDMSLHPLL
QEIYKDLY
Ligand information
Ligand ID
Z27
InChI
InChI=1S/C20H10Cl3F3N2O2S3/c21-11-2-4-17-15(8-11)27-19(32-17)31-16-5-3-12(9-13(16)22)28-33(29,30)18-6-1-10(7-14(18)23)20(24,25)26/h1-9,28H
InChIKey
BYUHFXVHEGWPSE-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 11.02
FC(F)(F)c1ccc(c(Cl)c1)S(=O)(=O)Nc4ccc(Sc2nc3cc(Cl)ccc3s2)c(Cl)c4
CACTVS 3.352
FC(F)(F)c1ccc(c(Cl)c1)[S](=O)(=O)Nc2ccc(Sc3sc4ccc(Cl)cc4n3)c(Cl)c2
OpenEye OEToolkits 1.7.0
c1cc(c(cc1C(F)(F)F)Cl)S(=O)(=O)Nc2ccc(c(c2)Cl)Sc3nc4cc(ccc4s3)Cl
Formula
C20 H10 Cl3 F3 N2 O2 S3
Name
2-chloro-N-{3-chloro-4-[(5-chloro-1,3-benzothiazol-2-yl)sulfanyl]phenyl}-4-(trifluoromethyl)benzenesulfonamide
ChEMBL
CHEMBL1236927
DrugBank
ZINC
ZINC000037868313
PDB chain
3k8s Chain B Residue 1 [
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Receptor-Ligand Complex Structure
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PDB
3k8s
T2384, a novel antidiabetic agent with unique peroxisome proliferator-activated receptor gamma binding properties
Resolution
2.55 Å
Binding residue
(original residue number in PDB)
L228 I281 F282 C285 R288 S289 I326 Y327 L330 L333 F360 F363 M364 K367 H449
Binding residue
(residue number reindexed from 1)
L22 I62 F63 C66 R69 S70 I107 Y108 L111 L114 F141 F144 M145 K148 H230
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0003677
DNA binding
GO:0004879
nuclear receptor activity
Biological Process
GO:0006355
regulation of DNA-templated transcription
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:3k8s
,
PDBe:3k8s
,
PDBj:3k8s
PDBsum
3k8s
PubMed
18263587
UniProt
P37231
|PPARG_HUMAN Peroxisome proliferator-activated receptor gamma (Gene Name=PPARG)
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