5H7Y

Structure of immunity protein TplEi of T6SS from Pseudomonas aeruginosa complexed with "L" peptide

5H7Y の概要

• エントリーDOI: 10.2210/pdb5h7y/pdb
• 関連するPDBエントリー: 5H7Z
• 分子名称: Uncharacterized protein (3 entities in total)
• 機能のキーワード: antimicrobial peptide, effector -immunity complex, inhibitor, hydrolase inhibitor-peptide complex, hydrolase inhibitor/peptide
• 由来する生物種: Pseudomonas aeruginosa PAO1; 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 45419.71

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: 2024-11-06)

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

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

実験手法

X-RAY DIFFRACTION (2.195 Å)