4W4L

Crystal structure of EspG5 in complex with PE25 and PPE41 from the ESX-5 type VII secretion system of M. tuberculosis

4W4L の概要

• エントリーDOI: 10.2210/pdb4w4l/pdb
• 関連するPDBエントリー: 4W4I 4W4J 4W4K
• 分子名称: PE family protein PE25, PPE family protein PPE41, EspG5, ... (5 entities in total)
• 機能のキーワード: ternary complex, signal recognition, virulence factor, protein secretion, protein transport
• 由来する生物種: Mycobacterium tuberculosis; 詳細
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 65311.30

構造登録者

Ekiert, D.C.,Cox, J.S. (登録日: 2014-08-14, 公開日: 2014-10-01, 最終更新日: 2023-09-27)

主引用文献

Ekiert, D.C.,Cox, J.S.
Structure of a PE-PPE-EspG complex from Mycobacterium tuberculosis reveals molecular specificity of ESX protein secretion.
Proc.Natl.Acad.Sci.USA, 111:14758-14763, 2014

PubMed Abstract: Nearly 10% of the coding capacity of the Mycobacterium tuberculosis genome is devoted to two highly expanded and enigmatic protein families called PE and PPE, some of which are important virulence/immunogenicity factors and are secreted during infection via a unique alternative secretory system termed "type VII." How PE-PPE proteins function during infection and how they are translocated to the bacterial surface through the five distinct type VII secretion systems [ESAT-6 secretion system (ESX)] of M. tuberculosis is poorly understood. Here, we report the crystal structure of a PE-PPE heterodimer bound to ESX secretion-associated protein G (EspG), which adopts a novel fold. This PE-PPE-EspG complex, along with structures of two additional EspGs, suggests that EspG acts as an adaptor that recognizes specific PE-PPE protein complexes via extensive interactions with PPE domains, and delivers them to ESX machinery for secretion. Surprisingly, secretion of most PE-PPE proteins in M. tuberculosis is likely mediated by EspG from the ESX-5 system, underscoring the importance of ESX-5 in mycobacterial pathogenesis. Moreover, our results indicate that PE-PPE domains function as cis-acting targeting sequences that are read out by EspGs, revealing the molecular specificity for secretion through distinct ESX pathways.

PubMed: 25275011
DOI: 10.1073/pnas.1409345111

実験手法

X-RAY DIFFRACTION (2.45 Å)