6I2N
Helical RNA-bound Hantaan virus nucleocapsid
6I2N の概要
| エントリーDOI | 10.2210/pdb6i2n/pdb |
| EMDBエントリー | 0333 |
| 分子名称 | RNA (5'-R(P*UP*UP*U)-3'), Nucleoprotein (2 entities in total) |
| 機能のキーワード | nucleoprotein, nucleocapsid, rna-binding, viral protein |
| 由来する生物種 | Hantaan orthohantavirus (Korean hemorrhagic fever virus) 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 49135.81 |
| 構造登録者 | Arragain, B.,Reguera, J.,Desfosses, A.,Gutsche, I.,Schoehn, G.,Malet, H. (登録日: 2018-11-01, 公開日: 2019-01-23, 最終更新日: 2024-05-15) |
| 主引用文献 | Arragain, B.,Reguera, J.,Desfosses, A.,Gutsche, I.,Schoehn, G.,Malet, H. High resolution cryo-EM structure of the helical RNA-bound Hantaan virus nucleocapsid reveals its assembly mechanisms. Elife, 8:-, 2019 Cited by PubMed Abstract: Negative-strand RNA viruses condense their genome into helical nucleocapsids that constitute essential templates for viral replication and transcription. The intrinsic flexibility of nucleocapsids usually prevents their full-length structural characterisation at high resolution. Here, we describe purification of full-length recombinant metastable helical nucleocapsid of Hantaan virus ( family, order) and determine its structure at 3.3 Å resolution by cryo-electron microscopy. The structure reveals the mechanisms of helical multimerisation via sub-domain exchanges between protomers and highlights nucleotide positions in a continuous positively charged groove compatible with viral genome binding. It uncovers key sites for future structure-based design of antivirals that are currently lacking to counteract life-threatening hantavirus infections. The structure also suggests a model of nucleoprotein-polymerase interaction that would enable replication and transcription solely upon local disruption of the nucleocapsid. PubMed: 30638449DOI: 10.7554/eLife.43075 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (3.3 Å) |
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