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Ized to cover different regions within the promoter of each relBE-like operon (Fig. 3, right panels; and Table S1 and Table S2). Using these specific DNA substrates, we examined the DNAbinding activities of each RelBE-like pair. As shown in Fig. 3A, no protein-DNA complex was observed using 1247p5 as a probe (first column). In contrast, a shifted band appeared with stepwise increases in the amount
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