3GWT
Catalytic domain of human phosphodiesterase 4B2B in complex with a quinoline inhibitor
Summary for 3GWT
Entry DOI | 10.2210/pdb3gwt/pdb |
Related | 3FRG |
Descriptor | cAMP-specific 3',5'-cyclic phosphodiesterase 4B, 6-{[3-(dimethylcarbamoyl)phenyl]sulfonyl}-4-[(3-methoxyphenyl)amino]-8-methylquinoline-3-carboxamide, ZINC ION, ... (7 entities in total) |
Functional Keywords | pde, phosphodiesterase, camp, hydrolase |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 41768.22 |
Authors | Somers, D.O.,Neu, M. (deposition date: 2009-04-01, release date: 2010-04-07, Last modification date: 2023-09-06) |
Primary citation | Woodrow, M.D.,Ballantine, S.P.,Barker, M.D.,Clarke, B.J.,Dawson, J.,Dean, T.W.,Delves, C.J.,Evans, B.,Gough, S.L.,Guntrip, S.B.,Holman, S.,Holmes, D.S.,Kranz, M.,Lindvaal, M.K.,Lucas, F.S.,Neu, M.,Ranshaw, L.E.,Solanke, Y.E.,Somers, D.O.,Ward, P.,Wiseman, J.O. Quinolines as a novel structural class of potent and selective PDE4 inhibitors. Optimisation for inhaled administration. Bioorg.Med.Chem.Lett., 19:5261-5265, 2009 Cited by PubMed: 19656678DOI: 10.1016/j.bmcl.2009.04.012 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.75 Å) |
Structure validation
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