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The PRNTase motifs are essential for the RNA capping activity of the RABV L protein: (a) The wild-type (WT) and mutant RABV L proteins (0.7 μg) were analyzed by SDS-PAGE as described in Figure 1a; (b) The WT and mutant RABV L proteins (0.1 μg) were subjected to in vitro capping reactions with [α-32P]GDP and pppAACAC. Lane 1 indicates no enzyme.
