The coronavirus disease 2019 (COVID-19) is caused by the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) which is pandemic with an estimated fatality rate less than 1% is ongoing. SARS-CoV-2 accessory proteins ORF3a, ORF6, ORF7a, ORF7b, ORF8, and ORF10 with putative functions to manipulate host immune mechanisms such as interferons, immune signaling receptor NLRP3 (NOD-, LRR-, and pyrin domain-containing 3) inflammasome, inflammatory cytokines such as interleukin β (IL-1β) are critical in COVID-19 pathology. Outspread variations of each of the six accessory proteins of all complete proteomes (available as of October 26, 2020, in the National Center for Biotechnology Information depository) of SARS-CoV-2, were observed across six continents. Across all continents, the decreasing order of percentage of unique variations in the accessory proteins was found to be ORF3a>ORF8>ORF7a>ORF6>ORF10>ORF7b. The highest and lowest unique variations of ORF3a were observed in South America and Oceania, respectively. This finding suggests that the wide variations of accessory proteins seem to govern the pathogenicity of SARS-CoV-2, and consequently, certain propositions and recommendations can be made in the public interest.
The aim of this paper is to make quantitative analysis of the properties which is really being carried from DNA sequence and finally landing up to the properties of a protein structure through its primary protein sequence. Thus, the paper has a theory which is applicable for any arbitrary DNA sequence whether it is of various species or mutated data or a bunch of genes responsible for a function to be occurred. Irrespective to genes of any families, species, wild type or mutated, our paper here gives a standard model which defines a mapping between physicochemical properties of any arbitrary DNA sequence and physicochemical properties of its amino acid sequence. Experiments have been carried out with PPCA protein family and its four homologs PPC(B-E) which establishes that DNA sequence keeps its signature even after its translation into the corresponding amino acid sequence.
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