review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Carlos G Vanoye | |
Charles R Sanders | |||
Wade D Van Horn | |||
P2860 | cites work | MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia | Q22009462 |
Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome | Q22010246 | ||
A constitutively open potassium channel formed by KCNQ1 and KCNE3 | Q22011154 | ||
Analysis of the interactions between the C-terminal cytoplasmic domains of KCNQ1 and KCNE1 channel subunits | Q24301528 | ||
The KCNQ1 (Kv7.1) COOH terminus, a multitiered scaffold for subunit assembly and protein interaction | Q24305236 | ||
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel | Q24318271 | ||
Mutations in the hminK gene cause long QT syndrome and suppress IKs function | Q24323571 | ||
Intracellular domains interactions and gated motions of I(KS) potassium channel subunits | Q24337820 | ||
KCNQ1 gain-of-function mutation in familial atrial fibrillation | Q24338486 | ||
Structural insight into KCNQ (Kv7) channel assembly and channelopathy | Q24619681 | ||
KCNE4 is an inhibitory subunit to the KCNQ1 channel | Q24642042 | ||
Atomic structure of a voltage-dependent K+ channel in a lipid membrane-like environment | Q27649044 | ||
Structure of the transmembrane regions of a bacterial cyclic nucleotide-regulated channel | Q27649693 | ||
Structure of KCNE1 and Implications for How It Modulates the KCNQ1 Potassium Channel † ‡ | Q27651069 | ||
Crystal structure of a trimeric form of the KV7.1 (KCNQ1) A-domain tail coiled-coil reveals structural plasticity and context dependent changes in a putative coiled-coil trimerization motif | Q27657087 | ||
X-ray structure, symmetry and mechanism of an AMPA-subtype glutamate receptor | Q27658372 | ||
A Gating Charge Transfer Center in Voltage Sensors | Q27660396 | ||
A common polymorphism associated with antibiotic-induced cardiac arrhythmia | Q28138550 | ||
Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2 | Q28145423 | ||
Protein-protein docking with simultaneous optimization of rigid-body displacement and side-chain conformations | Q28188949 | ||
MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis | Q28201439 | ||
A mutation in the KCNE3 potassium channel gene is associated with susceptibility to thyrotoxic hypokalemic periodic paralysis | Q28213064 | ||
A single transmembrane site in the KCNE-encoded proteins controls the specificity of KvLQT1 channel gating | Q28216718 | ||
Preparation, functional characterization, and NMR studies of human KCNE1, a voltage-gated potassium channel accessory subunit associated with deafness and long QT syndrome | Q28250352 | ||
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome | Q28251067 | ||
Crystal structure of a mammalian voltage-dependent Shaker family K+ channel | Q28260421 | ||
The conduction pore of a cardiac potassium channel | Q28262167 | ||
Cloning of a membrane protein that induces a slow voltage-gated potassium current | Q28292630 | ||
K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current | Q28295470 | ||
Long QT syndrome-associated mutations in KCNQ1 and KCNE1 subunits disrupt normal endosomal recycling of IKs channels | Q28300861 | ||
Stoichiometry of the KCNQ1 - KCNE1 ion channel complex. | Q28583726 | ||
Modeling structurally variable regions in homologous proteins with rosetta. | Q30341350 | ||
KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologs. | Q30776596 | ||
Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kinetics | Q33148043 | ||
The long QT syndrome: a prospective international study | Q33168684 | ||
S1 constrains S4 in the voltage sensor domain of Kv7.1 K+ channels | Q33327357 | ||
KCNE1 constrains the voltage sensor of Kv7.1 K+ channels | Q33327366 | ||
Functional interactions between KCNE1 C-terminus and the KCNQ1 channel | Q33425857 | ||
Mechanistic basis for LQT1 caused by S3 mutations in the KCNQ1 subunit of IKs. | Q33814293 | ||
A superfamily of small potassium channel subunits: form and function of the MinK-related peptides (MiRPs). | Q33857759 | ||
State-dependent electrostatic interactions of S4 arginines with E1 in S2 during Kv7.1 activation | Q33922794 | ||
Identification of a protein-protein interaction between KCNE1 and the activation gate machinery of KCNQ1 | Q33922814 | ||
KCNE1 remodels the voltage sensor of Kv7.1 to modulate channel function | Q34388706 | ||
Expression of multiple KCNE genes in human heart may enable variable modulation of I(Ks). | Q34392041 | ||
KCNQ1 channels voltage dependence through a voltage-dependent binding of the S4-S5 linker to the pore domain. | Q34452725 | ||
The KCNQ1 potassium channel: from gene to physiological function | Q34467640 | ||
The single nucleotide polymorphisms of I(Ks) potassium channel genes and their association with atrial fibrillation in a Chinese population | Q34570997 | ||
Voltage sensor conformations in the open and closed states in ROSETTA structural models of K(+) channels | Q34624463 | ||
KCNE regulation of KvLQT1 channels: structure-function correlates | Q34691356 | ||
Potassium channel subunits encoded by the KCNE gene family: physiology and pathophysiology of the MinK-related peptides (MiRPs). | Q35679326 | ||
Ion channels: function unravelled by dysfunction | Q35934207 | ||
KCNE peptides differently affect voltage sensor equilibrium and equilibration rates in KCNQ1 K+ channels | Q36325866 | ||
Single-channel properties of IKs potassium channels | Q36436185 | ||
MinK subdomains that mediate modulation of and association with KvLQT1. | Q36444720 | ||
Counting membrane-embedded KCNE beta-subunits in functioning K+ channel complexes | Q36446328 | ||
KCNQ1 and KCNE1 in the IKs channel complex make state-dependent contacts in their extracellular domains | Q36667897 | ||
Kv7.1 (KCNQ1) properties and channelopathies. | Q37049827 | ||
Sensing voltage across lipid membranes | Q37069037 | ||
Location of KCNE1 relative to KCNQ1 in the I(KS) potassium channel by disulfide cross-linking of substituted cysteines | Q37070508 | ||
Structural basis for K(V)7.1-KCNE(x) interactions in the I(Ks) channel complex | Q37412583 | ||
Delayed rectifier K(+) currents and cardiac repolarization. | Q37580457 | ||
Ancillary subunits associated with voltage-dependent K+ channels | Q37731213 | ||
KCNE1 binds to the KCNQ1 pore to regulate potassium channel activity | Q40543524 | ||
KCNE3 truncation mutants reveal a bipartite modulation of KCNQ1 K+ channels | Q41882406 | ||
Structural models for the KCNQ1 voltage-gated potassium channel | Q42001843 | ||
Closing in on the resting state of the Shaker K(+) channel. | Q42633636 | ||
Voltage sensor of Kv1.2: structural basis of electromechanical coupling | Q46588794 | ||
Restricting excessive cardiac action potential and QT prolongation: a vital role for IKs in human ventricular muscle. | Q46675989 | ||
Mechanisms by which atrial fibrillation-associated mutations in the S1 domain of KCNQ1 slow deactivation of IKs channels | Q48745779 | ||
The S4-S5 linker directly couples voltage sensor movement to the activation gate in the human ether-a'-go-go-related gene (hERG) K+ channel. | Q50651862 | ||
De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero. | Q50658517 | ||
Modulation of KCNQ1 current by atrial fibrillation-associated KCNE4 (145E/D) gene polymorphism. | Q51799237 | ||
Charybdotoxin Binding in the IKs Pore Demonstrates Two MinK Subunits in Each Channel Complex | Q58482877 | ||
MinK-KvLQT1 fusion proteins, evidence for multiple stoichiometries of the assembled IsK channel | Q77677778 | ||
P433 | issue | 2 | |
P304 | page(s) | 283-291 | |
P577 | publication date | 2011-02-04 | |
P1433 | published in | Current Opinion in Structural Biology | Q15758416 |
P1476 | title | Working model for the structural basis for KCNE1 modulation of the KCNQ1 potassium channel | |
P478 | volume | 21 |
Q42372905 | Are TMCs the Mechanotransduction Channels of Vertebrate Hair Cells? |
Q34566675 | Capturing distinct KCNQ2 channel resting states by metal ion bridges in the voltage-sensor domain |
Q38126397 | Domain structure and function of matrix metalloprotease 23 (MMP23): role in potassium channel trafficking |
Q36628028 | Dysfunctional potassium channel subunit interaction as a novel mechanism of long QT syndrome |
Q64244254 | Folding and Misfolding of Human Membrane Proteins in Health and Disease: From Single Molecules to Cellular Proteostasis |
Q34499486 | Fundamental role for the KCNE4 ancillary subunit in Kv7.4 regulation of arterial tone. |
Q84785186 | Genome-wide identification of possible methylation markers chemosensitive to targeted regimens in colorectal cancers |
Q36647350 | Intracellular trafficking of the KV1.3 potassium channel is regulated by the prodomain of a matrix metalloprotease |
Q27027928 | KCNQ1 channel modulation by KCNE proteins via the voltage-sensing domain |
Q38696328 | Photo-Cross-Linking of IKs Demonstrates State-Dependent Interactions between KCNE1 and KCNQ1. |
Q35893721 | Regulation of Voltage-Activated K(+) Channel Gating by Transmembrane β Subunits |
Q35621580 | Solution NMR approaches for establishing specificity of weak heterodimerization of membrane proteins |
Q53042866 | Steric hindrance between S4 and S5 of the KCNQ1/KCNE1 channel hampers pore opening. |
Q37245582 | Structural basis for KCNE3 modulation of potassium recycling in epithelia |
Q39477676 | Unnatural amino acid photo-crosslinking of the IKs channel complex demonstrates a KCNE1:KCNQ1 stoichiometry of up to 4:4. |
Q38690407 | Voltage-Dependent Gating: Novel Insights from KCNQ1 Channels |
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