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10.3390/ijms22010386

http://scihub22266oqcxt.onion/10.3390/ijms22010386
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33396557!7795774!33396557
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suck abstract from ncbi


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pmid33396557      Int+J+Mol+Sci 2020 ; 22 (1): ä
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  • Unpacking Pandora From Its Box: Deciphering the Molecular Basis of the SARS-CoV-2 Coronavirus #MMPMID33396557
  • O'Leary VB; Dolly OJ; Hoschl C; Cerna M; Ovsepian SV
  • Int J Mol Sci 2020[Dec]; 22 (1): ä PMID33396557show ga
  • An enigmatic localized pneumonia escalated into a worldwide COVID-19 pandemic from Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). This review aims to consolidate the extensive biological minutiae of SARS-CoV-2 which requires decipherment. Having one of the largest RNA viral genomes, the single strand contains the genes ORF1ab, S, E, M, N and ten open reading frames. Highlighting unique features such as stem-loop formation, slippery frameshifting sequences and ribosomal mimicry, SARS-CoV-2 represents a formidable cellular invader. Hijacking the hosts translational engine, it produces two polyprotein repositories (pp1a and pp1ab), armed with self-cleavage capacity for production of sixteen non-structural proteins. Novel glycosylation sites on the spike trimer reveal unique SARS-CoV-2 features for shielding and cellular internalization. Affording complexity for superior fitness and camouflage, SARS-CoV-2 challenges diagnosis and vaccine vigilance. This review serves the scientific community seeking in-depth molecular details when designing drugs to curb transmission of this biological armament.
  • |COVID-19/genetics/metabolism/*virology[MESH]
  • |Humans[MESH]
  • |Open Reading Frames[MESH]
  • |Pandemics[MESH]
  • |Phylogeny[MESH]
  • |RNA, Viral/genetics[MESH]
  • |SARS-CoV-2/*genetics/*metabolism[MESH]


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