Pdr5-mediated ATP hydrolysis. A, Vi-sensitive ATPase
activity of double-copy WT (•) or S558Y (▪) Pdr5 in purified PM
vesicles (10 mg per assay) was assayed as described previously
(5) in the presence of
increasing concentrations of ATP (0–3 mm ATP). B,
clotrimazole sensitivity of ATPase activity was monitored in WT purified
plasma membrane vesicles in the absence (•) or presence (▪) of 25
μm clotrimazole. C, clotrimazole sensitivity of ATPase
activity was monitored in the Pdr5 mutant, S558Y, purified plasma membrane
vesicles in the absence (•) or presence (▪) of 25 μm
clotrimazole. Representative plots are shown (n = 3).