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. 2024 Jul 4;14(7):797. doi: 10.3390/biom14070797

Figure 1.

Figure 1

Arrangement of the Mpro homodimer (built utilizing PDB complex: 7MGS [21]) and a comprehensive illustration of the viral N-terminal autoprocessing substrate nsp4/5 (depicted in yellow) while it is bound to its catalytic site, highlighting the catalytic residues His41 and Cys145 in orange.