4CDW
Crystal structure of human Enterovirus 71 in complex with the uncoating inhibitor GPP4
Summary for 4CDW
Entry DOI | 10.2210/pdb4cdw/pdb |
Related | 4CDQ 4CDU 4CDX 4CEW 4CEY |
Descriptor | VP1, VP2, VP3, ... (7 entities in total) |
Functional Keywords | virus, hand-foot-and-mouth disease, enterovirus uncoating, inhibitor |
Biological source | ENTEROVIRUS A71 More |
Total number of polymer chains | 4 |
Total formula weight | 94920.69 |
Authors | De Colibus, L.,Wang, X.,Spyrou, J.A.B.,Kelly, J.,Ren, J.,Grimes, J.,Puerstinger, G.,Stonehouse, N.,Walter, T.S.,Hu, Z.,Wang, J.,Li, X.,Peng, W.,Rowlands, D.,Fry, E.E.,Rao, Z.,Stuart, D.I. (deposition date: 2013-11-06, release date: 2014-02-12, Last modification date: 2024-05-08) |
Primary citation | De Colibus, L.,Wang, X.,Spyrou, J.A.B.,Kelly, J.,Ren, J.,Grimes, J.,Puerstinger, G.,Stonehouse, N.,Walter, T.S.,Hu, Z.,Wang, J.,Li, X.,Peng, W.,Rowlands, D.J.,Fry, E.E.,Rao, Z.,Stuart, D.I. More-Powerful Virus Inhibitors from Structure-Based Analysis of Hev71 Capsid-Binding Molecules Nat.Struct.Mol.Biol., 21:282-, 2014 Cited by PubMed Abstract: Enterovirus 71 (HEV71) epidemics in children and infants result mainly in mild symptoms; however, especially in the Asia-Pacific region, infection can be fatal. At present, no therapies are available. We have used structural analysis of the complete virus to guide the design of HEV71 inhibitors. Analysis of complexes with four 3-(4-pyridyl)-2-imidazolidinone derivatives with varying anti-HEV71 activities pinpointed key structure-activity correlates. We then identified additional potentially beneficial substitutions, developed methods to reliably triage compounds by quantum mechanics-enhanced ligand docking and synthesized two candidates. Structural analysis and in vitro assays confirmed the predicted binding modes and their ability to block viral infection. One ligand (with IC50 of 25 pM) is an order of magnitude more potent than the best previously reported inhibitor and is also more soluble. Our approach may be useful in the design of effective drugs for enterovirus infections. PubMed: 24509833DOI: 10.1038/NSMB.2769 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.8 Å) |
Structure validation
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