7QSA

Structural basis on the interaction of Scribble PDZ domains with the Tick Born encephalitis virus (TBEV) NS5 protein

7QSA の概要

• エントリーDOI: 10.2210/pdb7qsa/pdb
• 分子名称: Protein scribble homolog, RNA-directed RNA polymerase NS5 (3 entities in total)
• 機能のキーワード: tick born encephalitis virus, tbev, cell polarity, isothermal titration calorimetry, ns5, pdz, scribble, viral protein
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 20447.42

構造登録者

Javorsky, A.,Humbert, P.O.,Kvansakul, M. (登録日: 2022-01-13, 公開日: 2022-08-31, 最終更新日: 2024-01-31)

主引用文献

Javorsky, A.,Humbert, P.O.,Kvansakul, M.
Molecular basis of Tick Born encephalitis virus NS5 mediated subversion of apico-basal cell polarity signalling.
Biochem.J., 479:1303-1315, 2022

PubMed Abstract: The Scribble (Scrib) protein is a conserved cell polarity regulator with anti-tumorigenic properties. Viruses like the Tick-born encephalitis virus (TBEV) target Scribble to establish a cellular environment supporting viral replication, which is ultimately associated with poor prognosis upon infection. The TBEV NS5 protein has been reported to harbour both an internal as well as a C-terminal PDZ binding motif (PBM), however only the internal PBM was shown to be an interactor with Scribble, with the interaction being mediated via the Scribble PDZ4 domain to antagonize host interferon responses. We examined the NS5 PBM motif interactions with all Scribble PDZ domains using isothermal titration calorimetry, which revealed that the proposed internal PBM did not interact with any Scribble PDZ domains. Instead, the C-terminal PBM of NS5 interacted with Scrib PDZ3. We then established the structural basis of these interactions by determining crystal structures of Scrib PDZ3 bound to the NS5 C-terminal PBM. Our findings provide a structural basis for Scribble PDZ domain and TBEV NS5 interactions and provide a platform to dissect the pathogenesis of TBEV and the role of cell polarity signalling using structure guided approaches.

PubMed: 35670457
DOI: 10.1042/BCJ20220037

実験手法

X-RAY DIFFRACTION (2.02 Å)