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. 2011 Mar 1;286(16):13977–13984. doi: 10.1074/jbc.M111.227884

FIGURE 5.

FIGURE 5.

TASK-1 channels with multiple mutations at the drug binding site show a strong reduction of A1899 sensitivity. A, sample traces of TASK-1 wild-type, double, and triple mutant channels before (black) and after (gray) application of 400 nm A1899. B, inhibition of TASK-1 channels with multiple mutations by 400 nm A1899.