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. 2014 Jun 25;34(3):e00116. doi: 10.1042/BSR20140062

Table 1. ATPase activity of CL-Pgp and low-Cys mutants.

Protein ATPase activity* (μmole Pi/mg/min) Ks Verapamil (μM) Ki Cyclosporine A (μM)
Wt 3.5±0.66 4.8±1.8 2.0±0.8
C6Z 3.5±0.19 2.0±1.1 3.4±0.9
CL-Pgp 3.2±0.56 3.8±3.3 4.8±2.3

*Maximum verapamil-stimulated ATPase activity in the presence of 30 μM verapamil (mean±S.E.M.).

†Concentration required for half-maximal ATPase activity derived from plots of V versus [drug] in Figures 8A and 8C (mean±S.E.M.); similar plots were obtained for C6Z-Pgp (not shown).

‡Cyclosporine A concentration required for half-maximal inhibition of verapamil-stimulated ATPase in Figures 8B and 8D (mean±S.E.M.); similar plots were obtained for C6Z-Pgp (not shown).