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. 2004 Dec;124(6):759–771. doi: 10.1085/jgp.200409114

TABLE I.

Electrophysiological Properties of KCNE3 Truncation Mutants

τdeactivation (ms)
Construct V1/2 (mV) z Basal Activation, A2 fast slow
Q1 −23.8 ± 0.6 1.39 ± 0.03 0.03 ± 0.01 221 ± 10
E3 23.5 ± 2.5 0.75 ± 0.03 0.31 ± 0.02 14.9 ± 0.3 124 ± 5
Δ5-40 25.3 ± 5.1 0.81 ± 0.07 0.35 ± 0.03 19.1 ± 1.2 130 ± 5
Δ10-51 24.6 ± 5.5 1.00 ± 0.05 0.30 ± 0.02 14.4 ± 0.6 102 ± 4
Δ41-55 86.4 ± 7.4 0.51 ± 0.01 0.12 ± 0.01 10.9 ± 0.2 115 ± 3
Δ84 10.1 ± 1.3 0.67 ± 0.02 0.07 ± 0.01 ND ND
Δ10-51/Δ84 −10.0 ± 0.7 1.31 ± 0.05 0.14 ± 0.02 ND ND
D90N 27.8 ± 4.1 0.59 ± 0.02 0.28 ± 0.02 13.7 ± 0.4 156 ± 28
E1/E3 TM D76N 4.5 ± 4.3 0.82 ± 0.03 0.08 ± 0.01 ND ND

Data from individual activation curves and deactivation time constants in KD98, obtained from four to six oocytes. Activation curves were fit to a Boltzmann function as described in materials and methods. Values are mean ± SEM. Basal activation (A2) for all activation curves was determined by normalizing the data after the Boltzmann fit such that the maximal current fitting parameter (A1) was equal to 1. V1/2 is the voltage of half-maximal activation and z is the slope factor. Time constants of deactivation were fit to a single or double exponential as described in materials and methods. ND, not determined.