EMDB/PDB/SASBDBから引用されている文献のデータベース

キーワード
構造解析手法	All X線回折 NMR 電子顕微鏡小角散乱中性子線回折線維回折粉末回折赤外分光 EPR FRET 理論モデルハイブリッド
著者・登録者
ジャーナル
IF	>30 >20 >10 >5 all

タイトル	Assisted assembly of bacteriophage T7 core components for genome translocation across the bacterial envelope.
ジャーナル・号・ページ	Proc Natl Acad Sci U S A, Vol. 118, Issue 34, Year 2021
掲載日	2021年8月24日
著者	Mar Pérez-Ruiz / Mar Pulido-Cid / Juan Román Luque-Ortega / José María Valpuesta / Ana Cuervo / José L Carrascosa /
PubMed 要旨	In most bacteriophages, genome transport across bacterial envelopes is carried out by the tail machinery. In viruses of the family, in which the tail is not long enough to traverse the bacterial ...In most bacteriophages, genome transport across bacterial envelopes is carried out by the tail machinery. In viruses of the family, in which the tail is not long enough to traverse the bacterial wall, it has been postulated that viral core proteins assembled inside the viral head are translocated and reassembled into a tube within the periplasm that extends the tail channel. Bacteriophage T7 infects , and despite extensive studies, the precise mechanism by which its genome is translocated remains unknown. Using cryo-electron microscopy, we have resolved the structure of two different assemblies of the T7 DNA translocation complex composed of the core proteins gp15 and gp16. Gp15 alone forms a partially folded hexamer, which is further assembled upon interaction with gp16 into a tubular structure, forming a channel that could allow DNA passage. The structure of the gp15-gp16 complex also shows the location within gp16 of a canonical transglycosylase motif involved in the degradation of the bacterial peptidoglycan layer. This complex docks well in the tail extension structure found in the periplasm of T7-infected bacteria and matches the sixfold symmetry of the phage tail. In such cases, gp15 and gp16 that are initially present in the T7 capsid eightfold-symmetric core would change their oligomeric state upon reassembly in the periplasm. Altogether, these results allow us to propose a model for the assembly of the core translocation complex in the periplasm, which furthers understanding of the molecular mechanism involved in the release of T7 viral DNA into the bacterial cytoplasm.
リンク	Proc Natl Acad Sci U S A / PubMed:34417311 / PubMed Central
手法	EM (単粒子)
解像度	3.0 - 3.6 Å
構造データ	10911 6ysz EMDB-10911, PDB-6ysz: Cryo-EM structure of T7 bacteriophage DNA translocation gp15 core protein intermediate assembly 手法: EM (単粒子) / 解像度: 3.6 Å 10912 6yt5 EMDB-10912, PDB-6yt5: Cryo-EM structure of T7 bacteriophage DNA translocation gp15-gp16 core complex intermediate assembly 手法: EM (単粒子) / 解像度: 3.0 Å
由来	escherichia phage t7 (ファージ)
キーワード	VIRAL PROTEIN / DNA TRANSLOCATION / VIRAL INFECTION / PERIPLASMIC SPACE COMPLEX. / VIRAL COMPLEX / TRANS-GLYCOSYLASE ACTIVITY / CHAPERONE / PERIPLASMIC SPACE COMPLEX