6UOV
Cryo-EM reconstruction of the PrgHK periplasmic ring from Salmonella's needle complex assembled in the absence of the export apparatus
6UOV の概要
| エントリーDOI | 10.2210/pdb6uov/pdb |
| EMDBエントリー | 20833 |
| 分子名称 | Lipoprotein PrgK, Protein PrgH (2 entities in total) |
| 機能のキーワード | bacterial nanomachine, type iii secretion system, membrane protein |
| 由来する生物種 | Salmonella enterica subsp. enterica serovar Typhimurium 詳細 |
| タンパク質・核酸の鎖数 | 46 |
| 化学式量合計 | 1673357.04 |
| 構造登録者 | |
| 主引用文献 | Butan, C.,Lara-Tejero, M.,Li, W.,Liu, J.,Galan, J.E. High-resolution view of the type III secretion export apparatus in situ reveals membrane remodeling and a secretion pathway. Proc.Natl.Acad.Sci.USA, 116:24786-24795, 2019 Cited by PubMed Abstract: Type III protein secretion systems are essential virulence factors for many important pathogenic bacteria. The entire protein secretion machine is composed of several substructures that organize into a holostructure or injectisome. The core component of the injectisome is the needle complex, which houses the export apparatus that serves as a gate for the passage of the secreted proteins through the bacterial inner membrane. Here, we describe a high-resolution structure of the export apparatus of the type III secretion system in association with the needle complex and the underlying bacterial membrane, both in isolation and in situ. We show the precise location of the core export apparatus components within the injectisome and bacterial envelope and demonstrate that their deployment results in major membrane remodeling and thinning, which may be central for the protein translocation process. We also show that InvA, a critical export apparatus component, forms a multiring cytoplasmic conduit that provides a pathway for the type III secretion substrates to reach the entrance of the export gate. Combined with structure-guided mutagenesis, our studies provide major insight into potential mechanisms of protein translocation and injectisome assembly. PubMed: 31744874DOI: 10.1073/pnas.1916331116 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (3.5 Å) |
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