we used hydrogen deuterium exchange masss spec (HDX-MS) to define the exchange kinetics of PLC-y1 as it interacts with the kinase domain of FGFR1, and liposomes containing PIP2, in order to understand
The residue numbers of the functional (FS) and allosteric (AS) site residues were obtained from the literature (see main body of the article). In the fourth and fifth columns we mention whether there
Unprocessed SDS-PAGE gels related to the publication. Figure 3 and S3 display SDS-PAGE activity assay while Figure S5 displays SDS-PAGE activity assay as well as analytical gel filtration fractions re
