3DY6
PPARdelta complexed with an anthranilic acid partial agonist
Summary for 3DY6
Entry DOI | 10.2210/pdb3dy6/pdb |
Related | 1gwx |
Descriptor | Peroxisome proliferator-activated receptor delta, IODIDE ION, 2-({[3-(3,4-dihydroisoquinolin-2(1H)-ylsulfonyl)phenyl]carbonyl}amino)benzoic acid, ... (4 entities in total) |
Functional Keywords | ppar, nulear receptor, activator, dna-binding, metal-binding, nucleus, transcription, transcription regulation, zinc-finger |
Biological source | Homo sapiens (human) |
Cellular location | Nucleus: Q03181 |
Total number of polymer chains | 2 |
Total formula weight | 63033.99 |
Authors | Lambert, M.L.,Xu, R.,Shearer, B.G.,Wilson, T.M. (deposition date: 2008-07-25, release date: 2008-10-07, Last modification date: 2023-08-30) |
Primary citation | Shearer, B.G.,Patel, H.S.,Billin, A.N.,Way, J.M.,Winegar, D.A.,Lambert, M.H.,Xu, R.X.,Leesnitzer, L.M.,Merrihew, R.V.,Huet, S.,Willson, T.M. Discovery of a novel class of PPARdelta partial agonists Bioorg.Med.Chem.Lett., 18:5018-5022, 2008 Cited by PubMed Abstract: Anthranilic acid GW9371 was identified as a novel class of PPARdelta partial agonist through high-throughput screening. The design and synthesis of SAR analogues is described. GSK1115 and GSK7227 show potent partial agonism of the PPARdelta target genes CPT1a and PDK4 in skeletal muscle cells. PubMed: 18722772DOI: 10.1016/j.bmcl.2008.08.011 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.9 Å) |
Structure validation
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