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6LNT

Cryo-EM structure of immature Zika virus in complex with human antibody DV62.5 Fab

6LNT の概要
エントリーDOI10.2210/pdb6lnt/pdb
関連するPDBエントリー6LNU
EMDBエントリー0932 0934
分子名称Envelope protein, pre-membrane protein, Fab DV62.5 heavy-chain variable region, ... (5 entities in total)
機能のキーワードimmature zika virus, human antibody, virus
由来する生物種Homo sapiens (Human)
詳細
タンパク質・核酸の鎖数12
化学式量合計293954.06
構造登録者
Tan, T.Y.,Fibriansah, G.,Kostyuchenko, V.A.,Ng, T.S.,Lim, X.X.,Lim, X.N.,Shi, J.,Morais, M.C.,Corti, D.,Lok, S.M. (登録日: 2020-01-02, 公開日: 2020-02-26, 最終更新日: 2024-03-27)
主引用文献Tan, T.Y.,Fibriansah, G.,Kostyuchenko, V.A.,Ng, T.S.,Lim, X.X.,Zhang, S.,Lim, X.N.,Wang, J.,Shi, J.,Morais, M.C.,Corti, D.,Lok, S.M.
Capsid protein structure in Zika virus reveals the flavivirus assembly process.
Nat Commun, 11:895-895, 2020
Cited by
PubMed Abstract: Structures of flavivirus (dengue virus and Zika virus) particles are known to near-atomic resolution and show detailed structure and arrangement of their surface proteins (E and prM in immature virus or M in mature virus). By contrast, the arrangement of the capsid proteins:RNA complex, which forms the core of the particle, is poorly understood, likely due to inherent dynamics. Here, we stabilize immature Zika virus via an antibody that binds across the E and prM proteins, resulting in a subnanometer resolution structure of capsid proteins within the virus particle. Fitting of the capsid protein into densities shows the presence of a helix previously thought to be removed via proteolysis. This structure illuminates capsid protein quaternary organization, including its orientation relative to the lipid membrane and the genomic RNA, and its interactions with the transmembrane regions of the surface proteins. Results show the capsid protein plays a central role in the flavivirus assembly process.
PubMed: 32060358
DOI: 10.1038/s41467-020-14647-9
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (8 Å)
構造検証レポート
Validation report summary of 6lnt
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2026-04-22に公開中

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