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10.1016/j.imlet.2020.05.008

http://scihub22266oqcxt.onion/10.1016/j.imlet.2020.05.008
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32534867!7289111!32534867
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suck abstract from ncbi

pmid32534867      Immunol+Lett 2020 ; 224 (?): 38-39
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  • Sequence homology between human PARP14 and the SARS-CoV-2 ADP ribose 1 -phosphatase #MMPMID32534867
  • Webb TE; Saad R
  • Immunol Lett 2020[Aug]; 224 (?): 38-39 PMID32534867show ga
  • * There is amino acid sequence homology between the ADP-ribose binding sites of human PARP14 and SARS-CoV-2 ADRP. * This homology is even more pronounced in bat species. * The model proposed highlights the potential of the PARP axis to yield druggable targets for the treatment of COVID-19.
  • |Amino Acid Sequence[MESH]
  • |Animals[MESH]
  • |Betacoronavirus/*enzymology/genetics[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/enzymology/immunology/*virology[MESH]
  • |Host-Pathogen Interactions[MESH]
  • |Humans[MESH]
  • |Macrophage Activation[MESH]
  • |Macrophages/enzymology/immunology/virology[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/enzymology/immunology/*virology[MESH]
  • |Poly(ADP-ribose) Polymerases/chemistry/genetics/*metabolism[MESH]
  • |Pyrophosphatases/chemistry/genetics/*metabolism[MESH]
  • |SARS-CoV-2[MESH]
  • |Sequence Homology[MESH]
  • |T-Lymphocytes, Helper-Inducer/enzymology/immunology/virology[MESH]
  • |Th1-Th2 Balance[MESH]


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