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5FK9

Crystal structure of staphylococcal enterotoxin A F47A mutant in complex with a T cell receptor

5FK9 の概要
エントリーDOI10.2210/pdb5fk9/pdb
関連するPDBエントリー5FKA
分子名称T CELL RECEPTOR ALPHA CHAIN, T CELL RECEPTOR BETA CHAIN, ENTEROTOXIN TYPE A, ... (4 entities in total)
機能のキーワードimmune system, superantigen, staphylcococcal enterotoxin, t cell receptor, major histocompatibility complex
由来する生物種HOMO SAPIENS (HUMAN)
詳細
細胞内の位置Secreted: 5FK9
タンパク質・核酸の鎖数3
化学式量合計77632.17
構造登録者
Rodstrom, K.E.J.,Regenthal, P.,Lindkvist-Petersson, K. (登録日: 2015-10-15, 公開日: 2016-05-25, 最終更新日: 2024-10-16)
主引用文献Rodstrom, K.E.J.,Regenthal, P.,Bahl, C.,Ford, A.,Baker, D.,Lindkvist-Petersson, K.
Two Common Structural Motifs for Tcr Recognition by Staphylococcal Enterotoxins
Sci.Rep., 6:25796-, 2016
Cited by
PubMed Abstract: Superantigens are toxins produced by Staphylococcus aureus, called staphylococcal enterotoxins (abbreviated SEA to SEU). They can cross-link the T cell receptor (TCR) and major histocompatibility complex class II, triggering a massive T cell activation and hence disease. Due to high stability and toxicity, superantigens are potential agents of bioterrorism. Hence, antagonists may not only be useful in the treatment of disease but also serve as countermeasures to biological warfare. Of particular interest are inhibitors against SEA and SEB. SEA is the main cause of food poisoning, while SEB is a common toxin manufactured as a biological weapon. Here, we present the crystal structures of SEA in complex with TCR and SEE in complex with the same TCR, complemented with computational alanine-scanning mutagenesis of SEA, SEB, SEC3, SEE, and SEH. We have identified two common areas that contribute to the general TCR binding for these superantigens. This paves the way for design of single antagonists directed towards multiple toxins.
PubMed: 27180909
DOI: 10.1038/SREP25796
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3.1 Å)
構造検証レポート
Validation report summary of 5fk9
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2024-10-30に公開中

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