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4CDW

Crystal structure of human Enterovirus 71 in complex with the uncoating inhibitor GPP4

Summary for 4CDW
Entry DOI10.2210/pdb4cdw/pdb
Related4CDQ 4CDU 4CDX 4CEW 4CEY
DescriptorVP1, VP2, VP3, ... (7 entities in total)
Functional Keywordsvirus, hand-foot-and-mouth disease, enterovirus uncoating, inhibitor
Biological sourceENTEROVIRUS A71
More
Total number of polymer chains4
Total formula weight94920.69
Authors
Primary citationDe 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: 24509833
DOI: 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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數據於2024-11-06公開中

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