Population
Foot-and-mouth disease virus (FMDV) leader (L) protein, cell-free system, and transfected cells
Comparison
Specific mutations introduced into the L gene vs Wild-type FMDV L protein
Design
Preclinical
Authors
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Cys-23/His-120 mutations identify FMDV Lpro targets; leaves open antiviral translation beyond animal models.
Identifies key active-site residues (Cys-23 and His-120) essential for the proteolytic activity of the FMDV L proteinase.
Piccone et al. (1995) studied this question.
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