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Open AccessJournal ArticleDOI

Interface-based design of the favipiravir-binding site in SARS-CoV-2 RNA-dependent RNA polymerase reveals mutations conferring resistance to chain termination.

TLDR
In this article, the authors used high-throughput interface-based protein design to generate >100k designs of the favipiravir-binding site of RdRp and identify mutational hotspots.
About
This article is published in FEBS Letters.The article was published on 2021-09-01 and is currently open access. It has received 19 citations till now. The article focuses on the topics: Favipiravir & RNA-dependent RNA polymerase.

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Genomic Variations in the Structural Proteins of SARS-CoV-2 and Their Deleterious Impact on Pathogenesis: A Comparative Genomics Approach.

TL;DR: In this paper, a comparative genomics analysis of the structural proteins of SARS-CoV-2 has been performed to get deeper insights into the mechanism of pathogenesis, structure-function relationships and development of modern therapeutic approaches.
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Oral antiviral treatments for COVID-19: opportunities and challenges

TL;DR: In this paper , the authors present the potential pharmaceutical antiviral targets, including various host-based targets and viral based targets, and characterizes the first-generation anti-SARS-CoV-2 oral drugs (nirmatrelvir/ritonavir and molnupiravir).
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Identification of broad anti-coronavirus chemical agents for repurposing against SARS-CoV-2 and variants of concern

TL;DR: In this paper , an image-based multicycle infection procedure with α-coronavirus hCoV-229E-eGFP was performed in an arrayed chemical library screen of 5440 clinical and preclinical compounds.
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Lethal Mutagenesis of RNA Viruses and Approved Drugs with Antiviral Mutagenic Activity

TL;DR: Among approved nucleoside analogs, experiments with polioviruses and other RNA viruses suggested that ribavirin can be mutagenic, although its mechanism of action is not clear.
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Hotspot residues and resistance mutations in the nirmatrelvir-binding site of SARS-CoV-2 main protease: Design, identification, and correlation with globally circulating viral genomes

TL;DR: In this article , a high-throughput protein design technique, the hotspot residues, and signatures of adaptation of Mpro having the highest probability of mutating and rendering nirmatrelvir ineffective were identified.
References
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Journal ArticleDOI

WebLogo: A Sequence Logo Generator

TL;DR: WebLogo generates sequence logos, graphical representations of the patterns within a multiple sequence alignment that provide a richer and more precise description of sequence similarity than consensus sequences and can rapidly reveal significant features of the alignment otherwise difficult to perceive.
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A new coronavirus associated with human respiratory disease in China.

TL;DR: Phylogenetic and metagenomic analyses of the complete viral genome of a new coronavirus from the family Coronaviridae reveal that the virus is closely related to a group of SARS-like coronaviruses found in bats in China.
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Spike mutation D614G alters SARS-CoV-2 fitness.

TL;DR: Hamsters infected with SARS-CoV-2 expressing spike D614G (G614 virus) produced higher infectious titres in nasal washes and the trachea, but not in the lungs, supporting clinical evidence showing that the mutation enhances viral loads in the upper respiratory tract of COVID-19 patients and may increase transmission.
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