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The interaction between ClpX and FtsZ was measured by monitoring the fraction of ClpX ATP hydrolysis mutant, ClpX(E185Q), that co-pellets with FtsZ wild type or mutant protein in the presence of GTP. Pelleted ClpX(E185Q) and FtsZ was quantified by Coomassie staining of SDS-PAGE gels and densitometry. Data from at least 3 replicates are presented as mean ± SEM.
