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. 1997 Nov 25;94(24):13323–13328. doi: 10.1073/pnas.94.24.13323

Figure 1.

Figure 1

(A) Schematic representation of chimera AL1 (13) and derived mutants F4A-IF19,20AA. Repeats I and II were from the α1A subunit. L-type sequences that were inserted into the carp skeletal muscle α1S are shown as black transmembrane segments (IIIS6 and IVS6) with bold lines as adjacent S5-S6 connecting loops. (B) Sequence alignment (Lower) of transmembrane segments IIIS6 of chimera AL1 (the carp skeletal muscle α1S, see 33) and segments IIIS6 of the cardiac L-type α1C (34) and the class A α1A subunit (15). Homologous putative pore-orientated phenylalanines in segment IIIS6 of AL1 and alanine mutations are highlighted. (C) Schematic α-helical representation of amino acid sequence of repeat IIIS6 of chimera AL1 (shaded). Substituted putative pore-orientated amino acids of mutants F4A-F20A that are homologous between α1A and α1C are shown (solid).