7DYM

Pseudomonas aeruginosa TseT-TsiT complex

7DYM の概要

• エントリーDOI: 10.2210/pdb7dym/pdb
• 分子名称: Tox-REase-5 domain-containing protein, Imm52 domain-containing protein (2 entities in total)
• 機能のキーワード: t6ss, immunity, effector, nuclease, toxin
• 由来する生物種: Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 55037.61

構造登録者

She, Z. (登録日: 2021-01-22, 公開日: 2021-08-25, 最終更新日: 2024-11-20)

主引用文献

Wen, H.,Liu, G.,Geng, Z.,Zhang, H.,Li, Y.,She, Z.,Dong, Y.
Structure and SAXS studies unveiled a novel inhibition mechanism of the Pseudomonas aeruginosa T6SS TseT-TsiT complex.
Int.J.Biol.Macromol., 188:450-459, 2021

PubMed Abstract: The bacterial type VI secretion system (T6SS) is a powerful arsenal that fires many toxic effectors into neighboring cells to gain advantage over inter-bacterial competition and eukaryotic host infection. Meanwhile, the cognate immunity proteins of these effectors are employed to protect themselves from the virulence. TseT-TsiT is a newly discovered effector-immunity (E-I) protein pair secreted by T6SS of Pseudomonas aeruginosa. Our group had reported the crystal structure of TsiT before. Here, we report the crystal structure of P. aeruginosa TseT-TsiT complex at 3.1 Å resolution. The interface of TseT-TsiT is characterized in this work. Through structure and small angle X-ray scattering (SAXS) studies, we discover that the long C-terminal helix of TseT may be flexible. Combining the homolog comparison results, we propose that TseT may form an oligomer in favor of its putative nuclease activity. Although TsiT doesn't directly block the putative active-site of TseT, it may hinder the TseT's oligomerization process to neutralize its virulence.

PubMed: 34371041
DOI: 10.1016/j.ijbiomac.2021.08.029

実験手法

X-RAY DIFFRACTION (3.1 Å)