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口蹄疫病毒3C蛋白酶的结构分析:抗病毒药物的可行靶点?

Structural analysis of foot-and-mouth disease virus 3C protease: a viable target for antiviral drugs?

作者信息

Curry S, Roqué-Rosell N, Sweeney T R, Zunszain P A, Leatherbarrow R J

机构信息

Biophysics Section, Division of Cell and Molecular Biology, Blackett Laboratory, Imperial College, Exhibition Road, London SW7 2AZ, UK.

出版信息

Biochem Soc Trans. 2007 Jun;35(Pt 3):594-8. doi: 10.1042/BST0350594.

Abstract

Foot-and-mouth disease virus causes a major global agricultural problem that is difficult to control with existing vaccines. Structural analyses of the viral 3C protease not only have provided fresh insights into the catalytic mechanism of an unusual class of chymotrypsin-like cysteine proteases, but also are generating valuable information to drive the quest for effective antiviral therapies.

摘要

口蹄疫病毒引发了一个重大的全球农业问题,现有疫苗难以对其进行控制。对该病毒3C蛋白酶的结构分析不仅为一类不同寻常的类胰凝乳蛋白酶样半胱氨酸蛋白酶的催化机制提供了新见解,也为寻求有效的抗病毒疗法提供了有价值的信息。

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