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10.3389/fcimb.2021.765039

http://scihub22266oqcxt.onion/10.3389/fcimb.2021.765039
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suck abstract from ncbi


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pmid34722346      Front+Cell+Infect+Microbiol 2021 ; 11 (ä): 765039
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  • Genomic Variations in the Structural Proteins of SARS-CoV-2 and Their Deleterious Impact on Pathogenesis: A Comparative Genomics Approach #MMPMID34722346
  • Mohammad T; Choudhury A; Habib I; Asrani P; Mathur Y; Umair M; Anjum F; Shafie A; Yadav DK; Hassan MI
  • Front Cell Infect Microbiol 2021[]; 11 (ä): 765039 PMID34722346show ga
  • A continual rise in severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection causing coronavirus disease (COVID-19) has become a global threat. The main problem comes when SARS-CoV-2 gets mutated with the rising infection and becomes more lethal for humankind than ever. Mutations in the structural proteins of SARS-CoV-2, i.e., the spike surface glycoprotein (S), envelope (E), membrane (M) and nucleocapsid (N), and replication machinery enzymes, i.e., main protease (M(pro)) and RNA-dependent RNA polymerase (RdRp) creating more complexities towards pathogenesis and the available COVID-19 therapeutic strategies. This study analyzes how a minimal variation in these enzymes, especially in S protein at the genomic/proteomic level, affects pathogenesis. The structural variations are discussed in light of the failure of small molecule development in COVID-19 therapeutic strategies. We have performed in-depth sequence- and structure-based analyses of these proteins to get deeper insights into the mechanism of pathogenesis, structure-function relationships, and development of modern therapeutic approaches. Structural and functional consequences of the selected mutations on these proteins and their association with SARS-CoV-2 virulency and human health are discussed in detail in the light of our comparative genomics analysis.
  • |*COVID-19[MESH]
  • |*SARS-CoV-2[MESH]
  • |Genomics[MESH]
  • |Humans[MESH]
  • |Proteomics[MESH]


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