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10.1016/j.csbj.2021.03.025

http://scihub22266oqcxt.onion/10.1016/j.csbj.2021.03.025
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33815686!7997051!33815686
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suck abstract from ncbi


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pmid33815686      Comput+Struct+Biotechnol+J 2021 ; 19 (ä): 1889-1895
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  • Neuropilins: C-end rule peptides and their association with nociception and COVID-19 #MMPMID33815686
  • Jobe A; Vijayan R
  • Comput Struct Biotechnol J 2021[]; 19 (ä): 1889-1895 PMID33815686show ga
  • Viral internalization is aided by host cell surface receptors. In the case of SARS-CoV-2 and SARS-CoV, the primary host receptor is the angiotensin-converting enzyme 2 (ACE2). Considering the disparities in the transmission rate and viral tropism of the two coronaviruses, additional host factors were suspected. Recently, a novel host factor for SARS-CoV-2 entry, neuropilin-1 (NRP-1) has been identified. These receptors potentiate viral infection in the presence of other host factors like ACE2. Through its C-end rule (CendR) motif exposed following furin processing, the SARS-CoV-2 spike protein binds to the CendR pocket of NRP-1 and achieves cell entry through endocytosis. The binding of SARS-CoV-2 spike protein to the NRP-1 receptor interferes with the docking of its endogenous ligand VEGF-A, signaling that would otherwise promote nociception. This review looks at the function of neuropilins and how it contributes to SARS-CoV-2 infection and nociception.
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