Effects of serine phosphorylation on FAK peptide
binding to the Cas SH3 domain when Cas binding is restricted to site I
of His-FRNK. (A) Representative Western blot of peptide competition
assays by using GST-Cas SH3 and His-FRNK PIIA. As in Figure
5, components were incubated in the presence of increasing amounts (1,
10, 25, 50, or 100 μM) of each peptide and FRNK was detected by
immunoblotting with the mAb 2A7 and 125I
anti-mouse IgG. (B) Quantitation and graphical representation of
PhosphorImager data by using His-FRNK PIIA with 25 or 100
μM peptide competitor. Data are presented using the same methods
detailed in Figure 5.