Selected article for: "aa sequence and reference sequence"

Author: Martin Bartas; Václav Brázda; Natália Bohálová; Alessio Cantara; Adriana Volná; Tereza Stachurová; Katerina Malachová; Eva B. Jagelská; Otília Porubiaková; Jirí Cerven; Petr Pecinka
Title: In-depth Bioinformatic Analyses of Human SARS-CoV-2, SARS-CoV, MERS-CoV, and Other Nidovirales Suggest Important Roles of Noncanonical Nucleic Acid Structures in Their Lifecycles
  • Document date: 2020_4_11
  • ID: d3q0xel1_43
    Snippet: . CC-BY-ND 4.0 International license author/funder. It is made available under a The copyright holder for this preprint (which was not peer-reviewed) is the . https://doi.org/10.1101/2020.04.09.031252 doi: bioRxiv preprint This is a provisional file, not the final typeset article FIGURE 7 | Comparison of SUD domain M region in three pathogenic human coronaviruses. Nsp3 proteins of three pathogenic human viruses (SARS-CoV-2, SARS-CoV, and MERS-CoV.....
    Document: . CC-BY-ND 4.0 International license author/funder. It is made available under a The copyright holder for this preprint (which was not peer-reviewed) is the . https://doi.org/10.1101/2020.04.09.031252 doi: bioRxiv preprint This is a provisional file, not the final typeset article FIGURE 7 | Comparison of SUD domain M region in three pathogenic human coronaviruses. Nsp3 proteins of three pathogenic human viruses (SARS-CoV-2, SARS-CoV, and MERS-CoV) were aligned and part of the critical G-quadruplex binding M region of the SUD domain (525-577 aa according to the SARS-CoV reference sequence) was visualized. As predicted according to Kusov et al. (2015) , the G-quadruplex-interacting residues K565, K568, and E571 are highlighted in green (upper consensus panel).

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