Associated Papers
High-throughput functional mapping of variants in an arrhythmia gene, KCNE1, reveals novel biology.
Muhammad A et al.
Genome Medicine, 2024
38816749 (PubMed )
Supplement: 13073_2024_1340_MOESM3_ESM.xlsx › SpliceAI
Pharmacological rescue of specific long QT variants of KCNQ1/KCNE1 channels.
Zou X et al.
Frontiers in Physiology, 2022
Allosteric mechanism for KCNE1 modulation of KCNQ1 potassium channel activation.
Kuenze G et al.
Elife, 2020
33095155 (PubMed )
Supplement: elife-57680-fig7-data1.xlsx › Panel_C_-_Q1_activation_Vhalf
Probing Structural Dynamics and Topology of the KCNE1 Membrane Protein in Lipid Bilayers via Site-Directed Spin Labeling and Electron Paramagnetic Resonance Spectroscopy.
Sahu ID et al.
Biochemistry, 2015
Structural investigation of the transmembrane domain of KCNE1 in proteoliposomes.
Sahu ID et al.
Biochemistry, 2014
Regulation of Voltage-Activated K(+) Channel Gating by Transmembrane β Subunits.
Sun X et al.
Frontiers in Pharmacology, 2012
KCNQ1 subdomains involved in KCNE modulation revealed by an invertebrate KCNQ1 orthologue.
Nakajo K et al.
The Journal of General Physiology, 2011
TEA(+)-sensitive KCNQ1 constructs reveal pore-independent access to KCNE1 in assembled I(Ks) channels.
Kurokawa J et al.
The Journal of General Physiology, 2001
MinK subdomains that mediate modulation of and association with KvLQT1.
Tapper AR et al.
The Journal of General Physiology, 2000
MinK endows the I(Ks) potassium channel pore with sensitivity to internal tetraethylammonium.
Sesti F et al.
Biophysical Journal, 2000
Single-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome.
Sesti F et al.
The Journal of General Physiology, 1998
Select a paper to view details