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10.1002/pro.3936

http://scihub22266oqcxt.onion/10.1002/pro.3936
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32822073!7461438!32822073
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suck abstract from ncbi


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pmid32822073      Protein+Sci 2020 ; 29 (10): 2038-2042
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  • Comparing the binding properties of peptides mimicking the Envelope protein of SARS-CoV and SARS-CoV-2 to the PDZ domain of the tight junction-associated PALS1 protein #MMPMID32822073
  • Toto A; Ma S; Malagrino F; Visconti L; Pagano L; Stromgaard K; Gianni S
  • Protein Sci 2020[Oct]; 29 (10): 2038-2042 PMID32822073show ga
  • The Envelope protein (E) is one of the four structural proteins encoded by the genome of SARS-CoV and SARS-CoV-2 Coronaviruses. It is an integral membrane protein, highly expressed in the host cell, which is known to have an important role in Coronaviruses maturation, assembly and virulence. The E protein presents a PDZ-binding motif at its C-terminus. One of the key interactors of the E protein in the intracellular environment is the PDZ containing protein PALS1. This interaction is known to play a key role in the SARS-CoV pathology and suspected to affect the integrity of the lung epithelia. In this paper we measured and compared the affinity of peptides mimicking the E protein from SARS-CoV and SARS-CoV-2 for the PDZ domain of PALS1, through equilibrium and kinetic binding experiments. Our results support the hypothesis that the increased virulence of SARS-CoV-2 compared to SARS-CoV may rely on the increased affinity of its Envelope protein for PALS1.
  • |Amino Acid Sequence[MESH]
  • |Betacoronavirus/chemistry/*metabolism[MESH]
  • |Binding Sites[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Envelope Proteins[MESH]
  • |Coronavirus Infections/*metabolism/virology[MESH]
  • |Humans[MESH]
  • |Membrane Proteins/chemistry/*metabolism[MESH]
  • |Models, Molecular[MESH]
  • |Nucleoside-Phosphate Kinase/chemistry/*metabolism[MESH]
  • |PDZ Domains[MESH]
  • |Pandemics[MESH]
  • |Peptides/chemistry/metabolism[MESH]
  • |Pneumonia, Viral/*metabolism/virology[MESH]
  • |Protein Binding[MESH]
  • |SARS-CoV-2[MESH]
  • |Severe Acute Respiratory Syndrome/*metabolism/virology[MESH]
  • |Severe acute respiratory syndrome-related coronavirus/chemistry/*metabolism[MESH]


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