8EHO
PRRSV-1 PLP2 domain bound to ubiquitin
8EHO の概要
| エントリーDOI | 10.2210/pdb8eho/pdb |
| 関連するPDBエントリー | 8EHN |
| 分子名称 | Papain-like protease 2, Ubiquitin, ZINC ION, ... (7 entities in total) |
| 機能のキーワード | plp2, dub, deubiquitinating, viral protein |
| 由来する生物種 | Porcine reproductive and respiratory syndrome virus (PRRSV) 詳細 |
| タンパク質・核酸の鎖数 | 6 |
| 化学式量合計 | 92840.93 |
| 構造登録者 | |
| 主引用文献 | Bailey-Elkin, B.A.,Knaap, R.C.M.,De Silva, A.,Boekhoud, I.M.,Mous, S.,van Vught, N.,Khajehpour, M.,van den Born, E.,Kikkert, M.,Mark, B.L. Demonstrating the importance of porcine reproductive and respiratory syndrome virus papain-like protease 2 deubiquitinating activity in viral replication by structure-guided mutagenesis. Plos Pathog., 19:e1011872-e1011872, 2023 Cited by PubMed Abstract: Deubiquitination of cellular substrates by viral proteases is a mechanism used to interfere with host cellular signaling processes, shared between members of the coronavirus- and arterivirus families. In the case of Arteriviruses, deubiquitinating and polyprotein processing activities are accomplished by the virus-encoded papain-like protease 2 (PLP2). Several studies have implicated the deubiquitinating activity of the porcine reproductive and respiratory syndrome virus (PRRSV) PLP2 in the downregulation of cellular interferon production, however to date, the only arterivirus PLP2 structure described is that of equine arteritis virus (EAV), a distantly related virus. Here we describe the first crystal structure of the PRRSV PLP2 domain both in the presence and absence of its ubiquitin substrate, which reveals unique structural differences in this viral domain compared to PLP2 from EAV. To probe the role of PRRSV PLP2 deubiquitinating activity in host immune evasion, we selectively removed this activity from the domain by mutagenesis and found that the viral domain could no longer downregulate cellular interferon production. Interestingly, unlike EAV, and also unlike the situation for MERS-CoV, we found that recombinant PRRSV carrying PLP2 DUB-specific mutations faces significant selective pressure to revert to wild-type virus in MARC-145 cells, suggesting that the PLP2 DUB activity, which in PRRSV is present as three different versions of viral protein nsp2 expressed during infection, is critically important for PRRSV replication. PubMed: 38096325DOI: 10.1371/journal.ppat.1011872 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.85 Å) |
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