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10.1002/jmv.27009

http://scihub22266oqcxt.onion/10.1002/jmv.27009
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33837972!8250946!33837972
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suck abstract from ncbi


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pmid33837972      J+Med+Virol 2021 ; 93 (7): 4258-4264
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  • Coronavirus genomic nsp14-ExoN, structure, role, mechanism, and potential application as a drug target #MMPMID33837972
  • Tahir M
  • J Med Virol 2021[Jul]; 93 (7): 4258-4264 PMID33837972show ga
  • The recent coronavirus disease 2019 (COVID-19), causing a global pandemic with devastating effects on healthcare and social-economic systems, has no special antiviral therapies available for human coronaviruses (CoVs). The severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2) possesses a nonstructural protein (nsp14), with amino-terminal domain coding for proofreading exoribonuclease (ExoN) that is required for high-fidelity replication. The ability of CoVs during genome replication and transcription to proofread and exclude mismatched nucleotides has long hindered the development of anti-CoV drugs. The resistance of SARS-CoV-2 to antivirals, especially nucleoside analogs (NAs), shows the need to identify new CoV inhibition targets. Therefore, this review highlights the importance of nsp14-ExoN as a target for inhibition. Also, nucleoside analogs could be used in combination with existing anti-CoV therapeutics to target the proofreading mechanism.
  • |*COVID-19 Drug Treatment[MESH]
  • |Antiviral Agents/*pharmacology[MESH]
  • |Exoribonucleases/drug effects/*genetics/metabolism[MESH]
  • |Genome, Viral/genetics[MESH]
  • |Humans[MESH]
  • |Methyltransferases/genetics[MESH]
  • |RNA Processing, Post-Transcriptional/physiology[MESH]
  • |RNA, Viral/genetics[MESH]
  • |SARS-CoV-2/drug effects/*genetics[MESH]
  • |Viral Nonstructural Proteins/drug effects/*genetics/metabolism[MESH]


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