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• W1998719957 startingPage "14066" @default.
• W1998719957 abstract "Large conductance voltage- and Ca2+-dependent K+ (MaxiK) channels show sequence similarities to voltage-gated ion channels. They have a homologous S1-S6 region, but are unique at the N and C termini. At the C terminus, MaxiK channels have four additional hydrophobic regions (S7-S10) of unknown topology. At the N terminus, we have recently proposed a new model where MaxiK channels have an additional transmembrane region (S0) that confers beta subunit regulation. Using transient expression of epitope tagged MaxiK channels, in vitro translation, functional, and in vivo reconstitution assays, we now show that MaxiK channels have seven transmembrane segments (S0-S6) at the N terminus and a S1-S6 region that folds in a similar way as in voltage-gated ion channels. Further, our results indicate that hydrophobic segments S9-S10 in the C terminus are cytoplasmic and unequivocally demonstrate that S0 forms an additional transmembrane segment leading to an exoplasmic N terminus." @default.
• W1998719957 created "2016-06-24" @default.
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• W1998719957 date "1997-12-09" @default.
• W1998719957 modified "2023-10-11" @default.
• W1998719957 title "Large conductance voltage- and calcium-dependent K ⁺ channel, a distinct member of voltage-dependent ion channels with seven N-terminal transmembrane segments (S0-S6), an extracellular N terminus, and an intracellular (S9-S10) C terminus" @default.
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• W1998719957 doi "https://doi.org/10.1073/pnas.94.25.14066" @default.
• W1998719957 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/28433" @default.
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