2GTM
Mutated Mouse P38 MAP Kinase Domain in complex with Inhibitor PG-892579
Summary for 2GTM
Entry DOI | 10.2210/pdb2gtm/pdb |
Related | 1yw2 1ywr 2ghl 2ghm |
Descriptor | Mitogen-activated protein kinase 14, 8-(2-CHLOROPHENYLAMINO)-2-(2,6-DIFLUOROPHENYLAMINO)-9-ETHYL-9H-PURINE-1,7-DIIUM (3 entities in total) |
Functional Keywords | map kinase p38, p38, transferase |
Biological source | Mus musculus (house mouse) |
Cellular location | Cytoplasm : P47811 |
Total number of polymer chains | 1 |
Total formula weight | 40301.47 |
Authors | Walter, R.L.,Mekel, M.J.,Evdokimov, A.G.,Pokross, M.E.,Sabat, M. (deposition date: 2006-04-28, release date: 2006-05-23, Last modification date: 2024-04-03) |
Primary citation | Sabat, M.,Vanrens, J.C.,Clark, M.P.,Brugel, T.A.,Maier, J.,Bookland, R.G.,Laufersweiler, M.J.,Laughlin, S.K.,Golebiowski, A.,De, B.,Hsieh, L.C.,Walter, R.L.,Mekel, M.J.,Janusz, M.J. The development of novel C-2, C-8, and N-9 trisubstituted purines as inhibitors of TNF-alpha production. Bioorg.Med.Chem.Lett., 16:4360-4365, 2006 Cited by PubMed Abstract: A series of C-2, C-8, and N-9 trisubstituted purine based inhibitors of TNF-alpha production are described. The most potent analogs showed low nanomolar activity against LPS-induced TNF-alpha production in a THP-1 cell based assay. The SAR of the series was optimized with the aid of X-ray co-crystal structures of these inhibitors bound with mutated p38 (mp38). PubMed: 16750367DOI: 10.1016/j.bmcl.2006.05.050 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.9 Å) |
Structure validation
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