PDB ID: 6K0T
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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CTU | 3-[(1~{E})-1-[8-[(8-chloranyl-2-cyclopropyl-imidazo[1,2-a]pyridin-3-yl)methyl]-3-fluoranyl-6~{H}-benzo[C][1]benzoxepin-11-ylidene]ethyl]-4~{H}-1,2,4-oxadiazol-5-one | PoSSuM |
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CME | S,S-(2-hydroxyethyl)thiocysteine |
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Download interaction data: 6K0T
Structure summary
Code : | 6K0T PDBj RCSB PDB PDBe | ||||||||||||||||||||||||
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Header : | NUCLEAR PROTEIN | ||||||||||||||||||||||||
Title : | Crystal Structure of PPARgamma Ligand Binding Domain in complex with dibenzooxepine derivative compound-17 | ||||||||||||||||||||||||
Release Data : | 2019-10-30 | ||||||||||||||||||||||||
Compound : |
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Source : |
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Authors : | Suzuki, M., Yamamoto, K., Takahashi, Y., Saito, J. | ||||||||||||||||||||||||
Keywords : | PPARgamma, Ligand binding domain, PPARg modulator, Cancer, NUCLEAR PROTEIN | ||||||||||||||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.84 Å ) | ||||||||||||||||||||||||
Citation : |
Development of a novel class of peroxisome proliferator-activated receptor (PPAR) gamma ligands as an anticancer agent with a unique binding mode based on a non-thiazolidinedione scaffold.
Yamamoto, K.,Tamura, T.,Nakamura, R.
et al.
PubMed: 31623970 |
Reaction
Chain : | A, C |
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UniProt : | P37231 (PPARG_HUMAN) |
Reaction : | - |