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5H7Z

Apo structure of immunity protein TplEi of T6SS from Pseudomonas aeruginosa

5H7Z の概要
エントリーDOI10.2210/pdb5h7z/pdb
関連するPDBエントリー5H7Y
分子名称Uncharacterized protein, SULFATE ION (2 entities in total)
機能のキーワードantimicrobial peptide, effector -immunity complex, inhibitor, hydrolase inhibitor
由来する生物種Pseudomonas aeruginosa PAO1
タンパク質・核酸の鎖数2
化学式量合計85783.05
構造登録者
Gao, X.P.,Mu, Z.X.,Cui, S. (登録日: 2016-11-21, 公開日: 2017-10-04, 最終更新日: 2024-10-09)
主引用文献Gao, X.P.,Mu, Z.X.,Qin, B.,Sun, Y.,Cui, S.
Structure-Based Prototype Peptides Targeting the Pseudomonas aeruginosa Type VI Secretion System Effector as a Novel Antibacterial Strategy
Front Cell Infect Microbiol, 7:411-411, 2017
Cited by
PubMed Abstract: The type VI secretion system (T6SS) secretes numerous toxins for bacteria-bacteria competition. TplE is a newly identified trans-kingdom toxin secreted by the T6SS in , while TplEi neutralizes the toxic effect of TplE to protect bacteria autointoxication. Blocking the interaction of TplE-TplEi could unleash the toxin, causing bacterial cell death. In this study, we applied a crystallographic approach to design a structural-based antimicrobial peptides targeting the interaction of TplE and TplEi. We found that a peptide (designed as "L" peptide based on its shape) derived from TplE can form a crystal complex with TplEi after subtilisin treatment and the crystal structure was solved at 2.2Å. The "L" peptide displays strong binding affinity to TplEi and can release the TplE toxin to induce bacteria death . Our findings suggest that as a toxin activator, the "L" peptide could be a possible drug lead for treating infection. Our findings provide an example that the T6SS effector and immunity protein could be a potential drug target against bacteria infection.
PubMed: 28979890
DOI: 10.3389/fcimb.2017.00411
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3.057 Å)
構造検証レポート
Validation report summary of 5h7z
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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