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4CEY

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

4CEY の概要
エントリーDOI10.2210/pdb4cey/pdb
関連するPDBエントリー4CDQ 4CDU 4CDW 4CDX 4CEW
分子名称VP1, VP2, VP3, ... (7 entities in total)
機能のキーワードvirus, hand-foot-and-mouth disease, enterovirus uncoating, inhibitor
由来する生物種ENTEROVIRUS A71
詳細
細胞内の位置Host cytoplasmic vesicle membrane; Peripheral membrane protein; Cytoplasmic side (By similarity): B2ZUN0 B2ZUN0 B2ZUN0 B2ZUN0
タンパク質・核酸の鎖数4
化学式量合計94880.82
構造登録者
主引用文献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: 24509833
DOI: 10.1038/NSMB.2769
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.75 Å)
構造検証レポート
Validation report summary of 4cey
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-07-23に公開中

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