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10.1002/jmv.27132

http://scihub22266oqcxt.onion/10.1002/jmv.27132
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34125455!8427004!34125455
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suck abstract from ncbi


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pmid34125455      J+Med+Virol 2021 ; 93 (10): 5729-5741
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  • Molecular biology of the SARs-CoV-2 spike protein: A review of current knowledge #MMPMID34125455
  • Zhu C; He G; Yin Q; Zeng L; Ye X; Shi Y; Xu W
  • J Med Virol 2021[Oct]; 93 (10): 5729-5741 PMID34125455show ga
  • The global coronavirus disease 2019 (COVID-19) pandemic, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has led to an unprecedented worldwide public health emergency. Despite the concerted efforts of the scientific field, by April 25, 2021, SARS-CoV-2 had spread to over 192 countries/regions, causing more than 146 million confirmed cases including 31 million deaths. For now, an established treatment for patients with COVID-19 remains unavailable. The key to tackling this pandemic is to understand the mechanisms underlying its infectivity and pathogenicity. As a predominant focus, the coronavirus spike (S) protein is the key determinant of host range, infectivity, and pathogenesis. Thereby comprehensive understanding of the sophisticated structure of SARS-CoV-2 S protein may provide insights into possible intervention strategies to fight this ongoing global pandemic. Herein, we summarize the current knowledge of the molecular structural and functional features of SARS-CoV-2 S protein as well as recent updates on the cell entry mechanism of the SARS-CoV-2, paving the way for exploring more structure-guided strategies against SARS-CoV-2.
  • |COVID-19/virology[MESH]
  • |Host Specificity[MESH]
  • |Humans[MESH]
  • |Mutation[MESH]
  • |Protein Conformation[MESH]
  • |Protein Subunits[MESH]
  • |Receptors, Virus/genetics/metabolism[MESH]
  • |SARS-CoV-2/classification/pathogenicity/*physiology[MESH]
  • |Spike Glycoprotein, Coronavirus/*chemistry/genetics/*metabolism[MESH]


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  • suck abstract from ncbi

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