WNK1 [with no lysine (K)] is a serine-threonine kinase
associated with a form of familial hypertension. WNK1 is at the top of a kinase
cascade leading to phosphorylation of several cotransporters, in particular
those transporting sodium, potassium, and chloride (NKCC), sodium and chloride
(NCC), and potassium and chloride (KCC). The responsiveness of NKCC, NCC, and
KCC to changes in extracellular chloride parallels their phosphorylation state,
provoking the proposal that these transporters are controlled by a
chloride-sensitive protein kinase. Here, we found that chloride stabilizes the
inactive conformation of WNK1, preventing kinase autophosphorylation and
activation. Crystallographic studies of inactive WNK1 in the presence of
chloride revealed that chloride binds directly to the catalytic site, providing
a basis for the unique position of the catalytic lysine. Mutagenesis of the
chloride binding site rendered the kinase less sensitive to inhibition of
autophosphorylation by chloride, validating the binding site. Thus, these data
suggest that WNK1 functions as a chloride sensor through direct binding of a
regulatory chloride ion to the active site, which inhibits
autophosphorylation.
Background: MAPK cascades are signaling modules that function as switch generators. Results: In vitro phosphorylation in the p38 MAPK cascade tracked by LC-MS/MS revealed specific phosphorylation intermediates at each level. Conclusion: The p38 MAPK cascade reactions occur through intermediates MEK6/ST* and p38␣/TY*. Significance: The precise order of reactions may contribute to the diverse kinetic outputs of the cascades, including those with large Hill coefficients.
MAP kinase modules propagate diverse extracellular signals to downstream effectors. The two dual phosphorylation reactions catalyzed by the modules are thought to control the switch behavior of the pathway. Here we review recent approaches to understand these pathways through signal-to-response studies in cells and in vitro. These data are reconciled with physical models as well as predictions made on mathematical and theoretical grounds. Biochemical analysis has shown recently that the dual phosphorylation reactions catalyzed by MAP kinase modules are sequential at both levels of the cascade. The observed order of phosphorylation events suggests an excursion from the Ser/Thr kinase activity of the MAP3K into Tyr kinase activity of the central dual specificity MAP2K. How the order of events might be encoded in the structures and interactions is discussed. The ordered mechanism confirms predictions that reactions should be sequential to generate the steep signal-to-response curves and delayed responses observed in cells.
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