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Fig. 5. The GAP domain of RGA-2 enhances GTP hydrolysis by RHO-1 and CDC-42.
Results of GAP assays obtained by incubating purified GTPases and
GST-RGA-2GAP fusion protein in the presence of
[
32P]GTP (see Materials and methods), resolving the reaction
products by thin layer chromatography (see Fig. S3 in the supplementary
material), and quantifying the GTP/GDP fraction with a phosphorimager. Each
time point represents the fraction of GTP hydrolysed after 2 minutes as a
function of RGA-2GAP concentration. The graph is representative of
four independent experiments.