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6XDC

Cryo-EM structure of SARS-CoV-2 ORF3a

6XDC の概要
エントリーDOI10.2210/pdb6xdc/pdb
EMDBエントリー22136 22138 22139
分子名称ORF3a protein (1 entity in total)
機能のキーワードsars-cov-2, coronavirus, viroporin, ion channel, transport protein
由来する生物種Severe acute respiratory syndrome coronavirus 2 (2019-nCoV)
タンパク質・核酸の鎖数2
化学式量合計64331.80
構造登録者
Kern, D.M.,Hoel, C.M.,Brohawn, S.G. (登録日: 2020-06-10, 公開日: 2020-06-17, 最終更新日: 2024-05-15)
主引用文献Kern, D.M.,Sorum, B.,Mali, S.S.,Hoel, C.M.,Sridharan, S.,Remis, J.P.,Toso, D.B.,Kotecha, A.,Bautista, D.M.,Brohawn, S.G.
Cryo-EM structure of SARS-CoV-2 ORF3a in lipid nanodiscs.
Nat.Struct.Mol.Biol., 28:573-582, 2021
Cited by
PubMed Abstract: SARS-CoV-2 ORF3a is a putative viral ion channel implicated in autophagy inhibition, inflammasome activation and apoptosis. 3a protein and anti-3a antibodies are found in infected patient tissues and plasma. Deletion of 3a in SARS-CoV-1 reduces viral titer and morbidity in mice, suggesting it could be an effective target for vaccines or therapeutics. Here, we present structures of SARS-CoV-2 3a determined by cryo-EM to 2.1-Å resolution. 3a adopts a new fold with a polar cavity that opens to the cytosol and membrane through separate water- and lipid-filled openings. Hydrophilic grooves along outer helices could form ion-conduction paths. Using electrophysiology and fluorescent ion imaging of 3a-reconstituted liposomes, we observe Ca-permeable, nonselective cation channel activity, identify mutations that alter ion permeability and discover polycationic inhibitors of 3a activity. 3a-like proteins are found across coronavirus lineages that infect bats and humans, suggesting that 3a-targeted approaches could treat COVID-19 and other coronavirus diseases.
PubMed: 34158638
DOI: 10.1038/s41594-021-00619-0
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.9 Å)
構造検証レポート
Validation report summary of 6xdc
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2026-02-11に公開中

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