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6F2L

Crystal structure of the complex between PPARgamma LBD and the ligand LJ570: structure obtained from crystals of the apo-form soaked for 15 days.

Summary for 6F2L
Entry DOI10.2210/pdb6f2l/pdb
Related4JL4
DescriptorPeroxisome proliferator-activated receptor gamma, (2S)-3-(biphenyl-4-yl)-2-(biphenyl-4-yloxy)propanoic acid (3 entities in total)
Functional Keywordsnuclear receptor, transcription factor, complex with an agonist, transcription
Biological sourceHomo sapiens (Human)
Cellular locationNucleus: P37231
Total number of polymer chains2
Total formula weight69560.27
Authors
Pochetti, G.,Montanari, M. (deposition date: 2017-11-24, release date: 2018-01-10, Last modification date: 2024-02-07)
Primary citationLaghezza, A.,Piemontese, L.,Cerchia, C.,Montanari, R.,Capelli, D.,Giudici, M.,Crestani, M.,Tortorella, P.,Peiretti, F.,Pochetti, G.,Lavecchia, A.,Loiodice, F.
Identification of the First PPAR alpha / gamma Dual Agonist Able To Bind to Canonical and Alternative Sites of PPAR gamma and To Inhibit Its Cdk5-Mediated Phosphorylation.
J.Med.Chem., 61:8282-8298, 2018
Cited by
PubMed: 30199253
DOI: 10.1021/acs.jmedchem.8b00835
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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