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. 2005 Jan;187(2):629–638. doi: 10.1128/JB.187.2.629-638.2005

FIG. 6.

FIG. 6.

Effect of mutations affecting residues in helix 7 on MinE's ability to stimulate MinD ATPase. MinD, AAA, D152A, or D154A (6 μM) was incubated in ATPase buffer. MinE was added at various concentrations, and the ATPase activity was measured by the release of 32Pi from [γ-32P]ATP. WT, wild type.