Structurally, A789V may be significant due to its position near the catalytic motif C as well as the residue D700 in the motif A, however the overall protein structure suggests that all the mutations together may play a role in modifying the active site and facilitating nucleoside discrimination [160] , [161] .
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Inhibition of viral RNA-dependent RNA polymerases with clinically relevant nucleotide analogs.
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