7P4E
Crystal structure of PPARgamma in complex with compound FL217
Summary for 7P4E
Entry DOI | 10.2210/pdb7p4e/pdb |
Descriptor | Peroxisome proliferator-activated receptor gamma, ~{N}-[[4-(cyclopropylsulfonylamino)-2-(trifluoromethyl)phenyl]methyl]-1-[(3-fluorophenyl)methyl]indole-5-carboxamide, SULFATE ION, ... (5 entities in total) |
Functional Keywords | complex, structural genomics, structural genomics consortium, sgc, dna binding protein |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 1 |
Total formula weight | 32681.81 |
Authors | Ni, X.,Lillich, F.,Proschak, E.,Chaikuad, A.,Knapp, S.,Structural Genomics Consortium (SGC) (deposition date: 2021-07-11, release date: 2022-07-06, Last modification date: 2024-01-31) |
Primary citation | Lillich, F.F.,Willems, S.,Ni, X.,Kilu, W.,Borkowsky, C.,Brodsky, M.,Kramer, J.S.,Brunst, S.,Hernandez-Olmos, V.,Heering, J.,Schierle, S.,Kestner, R.I.,Mayser, F.M.,Helmstadter, M.,Gobel, T.,Weizel, L.,Namgaladze, D.,Kaiser, A.,Steinhilber, D.,Pfeilschifter, W.,Kahnt, A.S.,Proschak, A.,Chaikuad, A.,Knapp, S.,Merk, D.,Proschak, E. Structure-Based Design of Dual Partial Peroxisome Proliferator-Activated Receptor gamma Agonists/Soluble Epoxide Hydrolase Inhibitors. J.Med.Chem., 64:17259-17276, 2021 Cited by PubMed: 34818007DOI: 10.1021/acs.jmedchem.1c01331 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.4 Å) |
Structure validation
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