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4NSO

Crystal structure of the effector-immunity protein complex

4NSO の概要
エントリーDOI10.2210/pdb4nso/pdb
関連するPDBエントリー4NSR
分子名称Effector protein, Immunity protein (3 entities in total)
機能のキーワードhelix, peptidoglycan, protein binding
由来する生物種Vibrio cholerae O1 biovar El Tor
詳細
タンパク質・核酸の鎖数2
化学式量合計46841.88
構造登録者
Dong, C. (登録日: 2013-11-28, 公開日: 2014-04-16, 最終更新日: 2024-10-30)
主引用文献Zhang, J.,Zhang, H.,Gao, Z.,Hu, H.,Dong, C.,Dong, Y.H.
Structural basis for recognition of the type VI spike protein VgrG3 by a cognate immunity protein.
Febs Lett., 588:1891-1898, 2014
Cited by
PubMed Abstract: The bacterial type VI secretion system (T6SS) is used by donor cells to inject toxic effectors into receptor cells. The donor cells produce the corresponding immunity proteins to protect themselves against the effector proteins, thereby preventing their self-intoxication. Recently, the C-terminal domain of VgrG3 was identified as a T6SS effector. Information on the molecular mechanism of VgrG3 and its immunity protein TsaB has been lacking. Here, we determined the crystal structures of native TsaB and the VgrG3C-TsaB complex. VgrG3C adopts a canonical phage-T4-lysozyme-like fold. TsaB interacts with VgrG3C through molecular mimicry, and inserts into the VgrG3C pocket.
PubMed: 24751834
DOI: 10.1016/j.febslet.2014.04.016
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 4nso
検証レポート(詳細版)ダウンロードをダウンロード

236060

件を2025-05-14に公開中

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