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"These four alanine substitutions eliminated the ability of PKA to shift the voltage dependence of HCN4-Cx4 channels (V 1/2 = -105.0 +/- 3.7 mV, n = 8 in control, -107.5 +/- 1.7 mV, n = 6 in PKA; XREF_FIG and XREF_FIG), indicating that this regulatory site is obligatory for modulation of HCN4 by PKA."