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. 2022 Jan 18;66(1):e01748-21. doi: 10.1128/AAC.01748-21

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Copyright © 2022 Niimi et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

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FIG 5 — Lineweaver-Burk plots of the ATPase activities of wt Cdr1 and A713P in response to increasing inhibitor concentrations. (A) Top, wt Cdr1 with FK506. Concentrations were 0 (green diamond), 0.5 μM (blue square), and 1 μM (magenta triangle). Bottom, A713P with FK506. Concentrations were 0 (green diamond), 1 μM (blue square), and 10 μM (magenta triangle). (B) Top, wt Cdr1 with enniatin B. Concentrations were 0 (green diamond), 0.1 μM (blue square), and 0.5 μM (magenta triangle). Bottom, A713P with enniatin B. Concentrations were 0 (green diamond), 0.1 μM (blue square), and 10 μM (magenta triangle). (C) Top, wt Cdr1 with beauvericin. Concentrations were 0 (green diamond), 0.2 μM (blue square), and 0.5 μM (magenta triangle). Bottom, A713P with beauvericin. Concentrations were 0 (green diamond), 0.1 μM (blue square), and 2 μM (magenta triangle). (D) wt Cdr1 with oligomycin. Concentrations were 0 (green diamond), 0.5 μM (blue square), and 1 μM (magenta triangle). (E) wt Cdr1 with vanadate. Concentrations were 0 (green diamond), 0.5 μM (blue square), and 2 μM (magenta triangle).