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3VCB

C425S mutant of the C-terminal cytoplasmic domain of non-structural protein 4 from mouse hepatitis virus A59

3VCB の概要
エントリーDOI10.2210/pdb3vcb/pdb
分子名称RNA-directed RNA polymerase (2 entities in total)
機能のキーワードnew fold; homodimer, host membrane; multi-pass membrane protein, cytoplasmic, hydrolase, viral protein
由来する生物種Murine hepatitis virus
細胞内の位置Host cytoplasm, host perinuclear region (By similarity). Host membrane; Multi-pass membrane protein (By similarity): Q9J3E9
タンパク質・核酸の鎖数2
化学式量合計21169.71
構造登録者
Xu, X.,Lou, Z.,Ma, Y.,Chen, X.,Yang, Z.,Tong, X.,Zhao, Q.,Xu, Y.,Deng, H.,Bartlam, M.,Rao, Z. (登録日: 2012-01-03, 公開日: 2012-01-11, 最終更新日: 2024-02-28)
主引用文献Xu, X.,Lou, Z.,Ma, Y.,Chen, X.,Yang, Z.,Tong, X.,Zhao, Q.,Xu, Y.,Deng, H.,Bartlam, M.,Rao, Z.
Crystal structure of the C-terminal cytoplasmic domain of non-structural protein 4 from mouse hepatitis virus A59.
Plos One, 4:e6217-e6217, 2009
Cited by
PubMed Abstract: The replication of coronaviruses takes place on cytoplasmic double membrane vesicles (DMVs) originating in the endoplasmic reticulum (ER). Three trans-membrane non-structural proteins, nsp3, nsp4 and nsp6, are understood to be membrane anchors of the coronavirus replication complex. Nsp4 is localized to the ER membrane when expressed alone but is recruited into the replication complex in infected cells. It is revealed to contain four trans-membrane regions and its N- and C-termini are exposed to the cytosol.
PubMed: 19593433
DOI: 10.1371/journal.pone.0006217
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.4 Å)
構造検証レポート
Validation report summary of 3vcb
検証レポート(詳細版)ダウンロードをダウンロード

250059

件を2026-03-04に公開中

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