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10.1016/j.meegid.2020.104646

http://scihub22266oqcxt.onion/10.1016/j.meegid.2020.104646
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suck abstract from ncbi


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pmid33249264      Infect+Genet+Evol 2021 ; 87 (ä): 104646
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  • Coevolutionary forces shaping the fitness of SARS-CoV-2 spike glycoprotein against human receptor ACE2 #MMPMID33249264
  • Priya P; Shanker A
  • Infect Genet Evol 2021[Jan]; 87 (ä): 104646 PMID33249264show ga
  • The current global health problem caused by SARS-CoV-2 has challenged the scientific community in various ways. Therefore, worldwide several scientific groups are exploring SARS-CoV-2 from different aspects including its origin, spread, severe infectivity, and also to find a cure. It is now well known that spike glycoprotein helps SARS-CoV-2 to enter inside the human host through a cellular receptor ACE2. However, the role of coevolutionary forces that makes SARS-CoV-2 spike glycoprotein more fit towards its human host remains unexplored. Therefore, in present bioinformatics study we identify coevolving amino acids in spike glycoprotein. Additionally, the effects of coevolution on the stability of the spike glycoprotein as well as its binding with receptor ACE2 were predicted. The results clearly indicate that coevolutionary forces play a pivotal role in increasing the fitness of spike glycoprotein against ACE2.
  • |*Angiotensin-Converting Enzyme 2/metabolism[MESH]
  • |*Biological Evolution[MESH]
  • |Humans[MESH]
  • |Protein Binding[MESH]
  • |SARS-CoV-2/genetics/pathogenicity/*physiology[MESH]
  • |Spike Glycoprotein, Coronavirus/genetics/*physiology[MESH]


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