Properties of small rRNA methyltransferase RsmD: Mutational and kinetic study

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FIGURE 3.
FIGURE 3.

Interaction of 30S ribosomes devoid of G966 methylation with the methyltransferase RsmD in the presence of sinefungin monitored by chemical and enzymatic footprinting. Lanes A, C, G, U correspond to sequencing lanes in the presence of corresponding ddNTP; UN corresponds to untreated 30S subunits of 30S·RsmD complex; DMS, Keth, T1, and T2 each correspond to treatment with dimethyl sulfate, kethoxal, and RNases T1 and T2, respectively; +/− indicates the preincubation of unmethylated at G966 30S subunits with RsmD and sinefungin. Protected bases are marked by arrows.

This Article

  1. RNA 18: 1178-1185