Skip to main content
. 2009 Mar 9;106(13):5070–5075. doi: 10.1073/pnas.0806117106

Fig. 4.

Fig. 4.

Sensitivity of FGFR1 and Csk to redox regulation. (A) WT FGFR1 catalytic domain and a Cys-488–Ala mutant were purified. (B) WT Csk and a Glu-205–Ala mutant were purified. (C) The kinase activity (turnover number) of FGFR1 and FGFR1–Cys-488–Ala as a function of DTT concentration in the kinase assay. (D) The kinase activity (turnover number) of Csk and Csk–Glu-205–Ala as a function of DTT concentration in the kinase assay.