3SP6
Structural basis for iloprost as a dual PPARalpha/delta agonist
Summary for 3SP6
Entry DOI | 10.2210/pdb3sp6/pdb |
Related | 3SP9 |
Descriptor | Peroxisome proliferator-activated receptor alpha, Peroxisome proliferator-activated receptor gamma coactivator 1-beta, (5E)-5-[(3aS,4R,5R,6aS)-5-hydroxy-4-[(1E,3S,4R)-3-hydroxy-4-methyloct-1-en-6-yn-1-yl]hexahydropentalen-2(1H)-ylidene]pentanoic acid, ... (4 entities in total) |
Functional Keywords | ppar lbd, nuclear receptor fold, ligand binding, gene transcription, transcription |
Biological source | Homo sapiens (human) More |
Cellular location | Nucleus: Q07869 Q86YN6 |
Total number of polymer chains | 2 |
Total formula weight | 33916.59 |
Authors | |
Primary citation | Jin, L.,Lin, S.,Rong, H.,Zheng, S.,Jin, S.,Wang, R.,Li, Y. Structural basis for iloprost as a dual peroxisome proliferator-activated receptor alpha/delta agonist. J.Biol.Chem., 286:31473-31479, 2011 Cited by PubMed: 21775429DOI: 10.1074/jbc.M111.266023 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.21 Å) |
Structure validation
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