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4V96

The structure of a 1.8 MDa viral genome injection device suggests alternative infection mechanisms

これはPDB形式変換不可エントリーです。
4V96 の概要
エントリーDOI10.2210/pdb4v96/pdb
関連するPDBエントリー3U6X 3UH8
分子名称ORF48, ORF46, BPP (3 entities in total)
機能のキーワードdistal tail protein, receptor-binding protein, phage baseplate, host adsorption apparatus, genome injection device, viral protein
由来する生物種Lactococcus phage TP901-1
詳細
タンパク質・核酸の鎖数78
化学式量合計1776025.24
構造登録者
主引用文献Veesler, D.,Spinelli, S.,Mahony, J.,Lichiere, J.,Blangy, S.,Bricogne, G.,Legrand, P.,Ortiz-Lombardia, M.,Campanacci, V.,van Sinderen, D.,Cambillau, C.
Structure of the phage TP901-1 1.8 MDa baseplate suggests an alternative host adhesion mechanism.
Proc.Natl.Acad.Sci.USA, 109:8954-8958, 2012
Cited by
PubMed Abstract: Phages of the Caudovirales order possess a tail that recognizes the host and ensures genome delivery upon infection. The X-ray structure of the approximately 1.8 MDa host adsorption device (baseplate) from the lactococcal phage TP901-1 shows that the receptor-binding proteins are pointing in the direction of the host, suggesting that this organelle is in a conformation ready for host adhesion. This result is in marked contrast with the lactococcal phage p2 situation, whose baseplate is known to undergo huge conformational changes in the presence of Ca(2+) to reach its active state. In vivo infection experiments confirmed these structural observations by demonstrating that Ca(2+) ions are required for host adhesion among p2-like phages (936-species) but have no influence on TP901-1-like phages (P335-species). These data suggest that these two families rely on diverse adhesion strategies which may lead to different signaling for genome release.
PubMed: 22611190
DOI: 10.1073/pnas.1200966109
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3.8 Å)
構造検証レポート
Validation report summary of 4v96
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2026-02-04に公開中

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