I am struggling to figure out the relationship between proteins and phosphoproteins from LC-MS/MS datasets.
For example, if the protein concentration of a kinase is downregulated (due to any event), we can assume that the phosphorylation of its substrate should also be down. So, in the case of TiO2 enriched phospho-LC-MS/MS data, if the substrate is differentially downregulated, how we can identify whether it is due to protein concentration reduction or due to lack of phosphorylation?
Here the redundancy between kinase-substrate is ignored just to make explanation simpler.
And Is there any tool that take into considertion this aspect in system biology?