We have put CheY into a steady-state of phosphorylation using small molecule phospho-donors. NMR has shown that the conformational changes between active and inactive CheY are extensive. We are examining ways to slow down the rate of dephosphorylation. We are also trying to make stable analogs of the phospho-form. Finally, we are studying mutants of CheY to learn which parts of the conformational change are essential for signalling.
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