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10.1038/s41401-020-0485-4

http://scihub22266oqcxt.onion/10.1038/s41401-020-0485-4
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suck abstract from ncbi


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pmid32747721      Acta+Pharmacol+Sin 2020 ; 41 (9): 1141-1149
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  • Structural and functional properties of SARS-CoV-2 spike protein: potential antivirus drug development for COVID-19 #MMPMID32747721
  • Huang Y; Yang C; Xu XF; Xu W; Liu SW
  • Acta Pharmacol Sin 2020[Sep]; 41 (9): 1141-1149 PMID32747721show ga
  • Coronavirus disease 2019 is a newly emerging infectious disease currently spreading across the world. It is caused by a novel coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The spike (S) protein of SARS-CoV-2, which plays a key role in the receptor recognition and cell membrane fusion process, is composed of two subunits, S1 and S2. The S1 subunit contains a receptor-binding domain that recognizes and binds to the host receptor angiotensin-converting enzyme 2, while the S2 subunit mediates viral cell membrane fusion by forming a six-helical bundle via the two-heptad repeat domain. In this review, we highlight recent research advance in the structure, function and development of antivirus drugs targeting the S protein.
  • |*Betacoronavirus/drug effects/physiology[MESH]
  • |*Coronavirus Infections/drug therapy/virology[MESH]
  • |*Pandemics[MESH]
  • |*Pneumonia, Viral/drug therapy/virology[MESH]
  • |Antiviral Agents/*pharmacology[MESH]
  • |COVID-19[MESH]
  • |Drug Discovery/methods[MESH]
  • |Humans[MESH]
  • |SARS-CoV-2[MESH]
  • |Spike Glycoprotein, Coronavirus/*physiology[MESH]


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