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. 2014 Sep 18;37(9):656–663. doi: 10.14348/molcells.2014.0087

Fig. 1.

Fig. 1.

Schematic of the human KCNQ1 subunit topology showing amino acidmutations. (A) A sequence alignment of the KCNQ1 channel protein and the amino acid residues that were mutated CaM-binding sites IQ1 (373, 392) and IQ2 (539).