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. 2020 Jun 1:1–13. doi: 10.1080/07391102.2020.1772108

Figure 2.

Figure 2.

Sequence alignment showing high homology among proteases of various human CoVs strains. The residues conserved among the substrate-binding pocket of various CoV proteases and interacting with all the ligands in this study, namely N3 inhibitor, Wi-N and CAPE are highlighted for reference.