The first cluster consisted of sites located N‐terminally, specifically S109; S127; S138; S143, consistently showing a highly significant dephosphorylation in the LATS1/2, NF2 and PTPN14 mutants, and no or mild upregulation in the LATS1, LATS2, and RHOA mutants.
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Phosphorylation-linked complex profiling identifies assemblies required for Hippo signal integration.
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