Selected article for: "Bat CoV identity and Human SARS identity"
Author: Rajanish Giri; Taniya Bhardwaj; Meenakshi Shegane; Bhuvaneshwari R. Gehi; Prateek Kumar; Kundlik Gadhave
Title: Dark Proteome of Newly Emerged SARS-CoV-2 in Comparison with Human and Bat Coronaviruses
  • Document date: 2020_3_14
    • ID: n7ylgqfu_77
    Snippet: Nsp3 protein of SARS-CoV-2 contains several substituted residues throughout the protein. It is equally close with both Nsp3 proteins of Human SARS and Bat CoV sharing respective 76.69% and 76.31% identity (Supplementary Figure S2B) . According to our results, the mean PPIDs of Nsp3 proteins of SARS-CoV-2, Human SARS, and Bat CoV are 7.40%, 7.91%, and 7.78% respectively ( Table 3) . Graphs in Figures 21A, 21B , and 21C portray the tendency of Nsp3.....
    Document: Nsp3 protein of SARS-CoV-2 contains several substituted residues throughout the protein. It is equally close with both Nsp3 proteins of Human SARS and Bat CoV sharing respective 76.69% and 76.31% identity (Supplementary Figure S2B) . According to our results, the mean PPIDs of Nsp3 proteins of SARS-CoV-2, Human SARS, and Bat CoV are 7.40%, 7.91%, and 7.78% respectively ( Table 3) . Graphs in Figures 21A, 21B , and 21C portray the tendency of Nsp3 proteins of SARS-CoV-2, Human SARS, and Bat CoV for the intrinsic disorder. Nsp3 proteins of all three studied SARS viruses were found to be highly structured and characterized by rather similar disorder profiles. This is further supported by Figure 21E , where PONDR ® VSL2-generated disorder profiles of these three proteins are overlapped to show almost complete coincidence of their major disorder-related features. According to the author/funder. All rights reserved. No reuse allowed without permission.

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