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. 2000 Jul 17;19(14):3704–3713. doi: 10.1093/emboj/19.14.3704

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Fig. 4. Comparison of GBD–Zap1 and myc-Zap1 activities in response to a range of zinc concentrations. (A) A zap1 mutant strain (ZHY6) bearing the pDg2 ZRE-lacZ reporter and pGBD–Zap11–880 (filled squares), pGBD–Zap1Δ553–686 (filled diamonds) or pGBD–Zap1552–880 (open circles) was grown to exponential phase in LZM supplemented with the indicated concentrations of ZnCl2 prior to assay for β-galactosidase activity. (B) The same zap1 mutant strain bearing the pDg2 ZRE-lacZ reporter and pMyc-Zap11–880 (filled squares), pMyc-Zap1Δ553–686 (filled diamonds) or pMyc-Zap1552–880 (open circles) was grown to exponential phase in LZM supplemented with the indicated concentrations of ZnCl2 prior to assay for β-galactosidase activity. Shown are representative experiments in which the standard deviations were <10% of the corresponding mean.