8DQU
Nanobody bound SARS-CoV-2 Nsp9
8DQU の概要
| エントリーDOI | 10.2210/pdb8dqu/pdb |
| 分子名称 | Nanobody, Non-structural protein 9 (3 entities in total) |
| 機能のキーワード | sars-cov-2, nsp9, nanobody, viral protein |
| 由来する生物種 | Lama glama 詳細 |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 56691.53 |
| 構造登録者 | |
| 主引用文献 | Pan, Y.,Chandrashekaran, I.R.,Tennant, L.,Rossjohn, J.,Littler, D.R. Inside-out: Antibody-binding reveals potential folding hinge-points within the SARS-CoV-2 replication co-factor nsp9. Plos One, 18:e0283194-e0283194, 2023 Cited by PubMed Abstract: Nsp9 is a conserved accessory component of the coronaviral replication and transcription complex. It is the predominant substrate of nsp12's nucleotidylation activity while also serving to recruit proteins required for viral 5'-capping. Anti-nsp9 specific nanobodies have been isolated previously. We confirm that their binding mode is centred upon Trp-53 within SARS-CoV-2 nsp9. Antibody binding at this site surprisingly results in large-scale changes to the overall topology of this coronaviral unique fold. We further characterise the antibody-induced structural dynamism within nsp9, identifying a number of potentially flexible regions. A large expansion of the cavity between the s2-s3 and s4-s5 loops is particularly noteworthy. As is the potential for large-scale movements in the C-terminal GxxxG helix. PubMed: 37036856DOI: 10.1371/journal.pone.0283194 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.45003185971 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






