5KO3

Structure of a Core Papain-like Protease of MERS Coronavirus with utility for structure-based drug design

5KO3 の概要

• エントリーDOI: 10.2210/pdb5ko3/pdb
• 分子名称: ORF1a, ZINC ION, ACETATE ION, ... (4 entities in total)
• 機能のキーワード: mers plpro, substrate-binding loop, hydrolase
• 由来する生物種: Middle East respiratory syndrome coronavirus
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 29209.19

構造登録者

Clasman, J.C.,Baez-Santos, Y.M.,Mesecar, A.D. (登録日: 2016-06-29, 公開日: 2017-01-25, 最終更新日: 2024-10-09)

主引用文献

Clasman, J.R.,Baez-Santos, Y.M.,Mettelman, R.C.,O'Brien, A.,Baker, S.C.,Mesecar, A.D.
X-ray Structure and Enzymatic Activity Profile of a Core Papain-like Protease of MERS Coronavirus with utility for structure-based drug design.
Sci Rep, 7:40292-40292, 2017

PubMed Abstract: Ubiquitin-like domain 2 (Ubl2) is immediately adjacent to the N-terminus of the papain-like protease (PLpro) domain in coronavirus polyproteins, and it may play a critical role in protease regulation and stability as well as in viral infection. However, our recent cellular studies reveal that removing the Ubl2 domain from MERS PLpro has no effect on its ability to process the viral polyprotein or act as an interferon antagonist, which involves deubiquitinating and deISGylating cellular proteins. Here, we test the hypothesis that the Ubl2 domain is not required for the catalytic function of MERS PLpro in vitro. The X-ray structure of MERS PLpro-∆Ubl2 was determined to 1.9 Å and compared to PLpro containing the N-terminal Ubl2 domain. While the structures were nearly identical, the PLpro-∆Ubl2 enzyme revealed the intact structure of the substrate-binding loop. Moreover, PLpro-∆Ubl2 catalysis against different substrates and a purported inhibitor revealed no differences in catalytic efficiency, substrate specificity, and inhibition. Further, no changes in thermal stability were observed between enzymes. We conclude that the catalytic core of MERS PLpro, i.e. without the Ubl2 domain, is sufficient for catalysis and stability in vitro with utility to evaluate potential inhibitors as a platform for structure-based drug design.

PubMed: 28079137
DOI: 10.1038/srep40292

実験手法

X-RAY DIFFRACTION (1.949 Å)