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10.1159/000513530

http://scihub22266oqcxt.onion/10.1159/000513530
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33406522!7900485!33406522
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suck abstract from ncbi


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pmid33406522      Public+Health+Genomics 2021 ; 24 (1-2): 54-66
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  • Genetic Variation and Evolution of the 2019 Novel Coronavirus #MMPMID33406522
  • Dimonte S; Babakir-Mina M; Hama-Soor T; Ali S
  • Public Health Genomics 2021[]; 24 (1-2): 54-66 PMID33406522show ga
  • INTRODUCTION: SARS-CoV-2 is a new type of coronavirus causing a pandemic severe acute respiratory syndrome (SARS-2). Coronaviruses are very diverting genetically and mutate so often periodically. The natural selection of viral mutations may cause host infection selectivity and infectivity. METHODS: This study was aimed to indicate the diversity between human and animal coronaviruses through finding the rate of mutation in each of the spike, nucleocapsid, envelope, and membrane proteins. RESULTS: The mutation rate is abundant in all 4 structural proteins. The most number of statistically significant amino acid mutations were found in spike receptor-binding domain (RBD) which may be because it is responsible for a corresponding receptor binding in a broad range of hosts and host selectivity to infect. Among 17 previously known amino acids which are important for binding of spike to angiotensin-converting enzyme 2 (ACE2) receptor, all of them are conservative among human coronaviruses, but only 3 of them significantly are mutated in animal coronaviruses. A single amino acid aspartate-454, that causes dissociation of the RBD of the spike and ACE2, and F486 which gives the strength of binding with ACE2 remain intact in all coronaviruses. DISCUSSION/CONCLUSION: Observations of this study provided evidence of the genetic diversity and rapid evolution of SARS-CoV-2 as well as other human and animal coronaviruses.
  • |*Coronavirus/classification/genetics/physiology[MESH]
  • |*SARS-CoV-2/genetics/physiology[MESH]
  • |*Viral Proteins/genetics/metabolism[MESH]
  • |Animals[MESH]
  • |COVID-19/*virology[MESH]
  • |Evolution, Molecular[MESH]
  • |Genetic Variation/*physiology[MESH]
  • |Host Microbial Interactions/genetics[MESH]


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