High resolution structures of the SARS-CoV-2 N7-methyltransferase inform therapeutic development.

IF 0.1 Q4 EDUCATION & EDUCATIONAL RESEARCH Sophia-Educacion Pub Date : 2022-03-08 DOI:10.21203/rs.3.rs-1370473/v1
Aneel Aggarwal, Jithesh Kottur
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引用次数: 0

Abstract

Emergence of SARS-CoV-2 coronavirus has led to millions of deaths globally. We present three high-resolution crystal structures of the SARS-CoV-2 nsp14 N7-methyltransferase core bound to S-adenosylmethionine (SAM; 1.62Å), S-adenosylhomocysteine (SAH; 1.55Å) and Sinefungin (SFG; 1.41Å). We identify features of the methyltransferase core that are crucial for the development of antivirals and show SAH as the best scaffold for the design of antivirals against SARS-CoV-2 and other pathogenic coronaviruses.

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SARS-CoV-2 N7-甲基转移酶的高分辨率结构为治疗开发提供了信息。
SARS-CoV-2 冠状病毒的出现导致全球数百万人死亡。我们展示了 SARS-CoV-2 nsp14 N7-甲基转移酶核心与 S-腺苷蛋氨酸(SAM;1.62 Å)、S-腺苷高半胱氨酸(SAH;1.55 Å)和辛弗宁(SFG;1.41 Å)结合的三个高分辨率晶体结构。我们确定了甲基转移酶核心对开发抗病毒药物至关重要的特征,并表明 SAH 是设计抗 SARS-CoV-2 和其他致病性冠状病毒药物的最佳支架。
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Sophia-Educacion
Sophia-Educacion EDUCATION & EDUCATIONAL RESEARCH-
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