| scholarly article | Q13442814 |
| P356 | DOI | 10.1074/JBC.M212824200 |
| P698 | PubMed publication ID | 12902341 |
| P50 | author | Terence J Campbell | Q58231955 |
| Jamie Vandenberg | Q42353728 | ||
| Margaret Sunde | Q46732256 | ||
| P2093 | author name string | Asne Bauskin | |
| Allan M Torres | |||
| Philip W Kuchel | |||
| Samuel N Breit | |||
| Paul F Alewood | |||
| David J Smith | |||
| Catherine E Clarke | |||
| Paramjit S Bansal | |||
| Jane A Bursill | |||
| P2860 | cites work | The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity | Q22337058 |
| X-ray structure of a voltage-dependent K+ channel | Q22337257 | ||
| A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel | Q24316252 | ||
| A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome | Q24316980 | ||
| The inward rectification mechanism of the HERG cardiac potassium channel | Q24320034 | ||
| A family of potassium channel genes related to eag in Drosophila and mammals | Q24563554 | ||
| Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination | Q26778405 | ||
| Transfer of rapid inactivation and sensitivity to the class III antiarrhythmic drug E-4031 from HERG to M-eag channels | Q47786553 | ||
| Molecular determinants of dofetilide block of HERG K+ channels | Q48945449 | ||
| Molecular determinants for activation and inactivation of HERG, a human inward rectifier potassium channel. | Q50761875 | ||
| Structures of the M2 channel-lining segments from nicotinic acetylcholine and NMDA receptors by NMR spectroscopy | Q27617929 | ||
| Crystal structure and mechanism of a calcium-gated potassium channel | Q27639064 | ||
| Crystal structure of the potassium channel KirBac1.1 in the closed state | Q27641201 | ||
| Torsion angle dynamics for NMR structure calculation with the new program DYANA | Q27860808 | ||
| Gradient-tailored excitation for single-quantum NMR spectroscopy of aqueous solutions | Q27860828 | ||
| MOLMOL: a program for display and analysis of macromolecular structures | Q27860873 | ||
| The program XEASY for computer-supported NMR spectral analysis of biological macromolecules | Q27860993 | ||
| Potassium channel structures | Q28218200 | ||
| The chemical shift index: a fast and simple method for the assignment of protein secondary structure through NMR spectroscopy | Q28293625 | ||
| State-dependent barium block of wild-type and inactivation-deficient HERG channels in Xenopus oocytes | Q28344460 | ||
| A structural basis for drug-induced long QT syndrome | Q28344808 | ||
| Properties of HERG channels stably expressed in HEK 293 cells studied at physiological temperature | Q28379324 | ||
| A two-dimensional nuclear Overhauser enhancement (2D NOE) experiment for the elucidation of complete proton-proton cross-relaxation networks in biological macromolecules | Q29616473 | ||
| Application of phase sensitive two-dimensional correlated spectroscopy (COSY) for measurements of 1H-1H spin-spin coupling constants in proteins | Q29616474 | ||
| Intrinsic helical propensities and stable secondary structure in a membrane-bound fragment (S4) of the shaker potassium channel | Q30583519 | ||
| Stability of membrane proteins: relevance for the selection of appropriate methods for high-resolution structure determinations | Q32065676 | ||
| The moving parts of voltage-gated ion channels | Q33671684 | ||
| An ERG channel inhibitor from the scorpion Buthus eupeus | Q33929814 | ||
| The long QT syndromes: genetic basis and clinical implications | Q33970623 | ||
| The potential for QT prolongation and proarrhythmia by non-antiarrhythmic drugs: clinical and regulatory implications. Report on a policy conference of the European Society of Cardiology | Q33989507 | ||
| Potassium channels: from scorpion venoms to high-resolution structure | Q34117953 | ||
| Effects of outer mouth mutations on hERG channel function: a comparison with similar mutations in the Shaker channel | Q34170649 | ||
| Molecular and cellular mechanisms of cardiac arrhythmias | Q34175373 | ||
| HERG K+ channels: friend and foe. | Q34243160 | ||
| I(Kr): the hERG channel | Q34245075 | ||
| Inhibition of HERG channels stably expressed in a mammalian cell line by the antianginal agent perhexiline maleate | Q35028771 | ||
| Fast inactivation causes rectification of the IKr channel | Q36411776 | ||
| Extracellular sodium interacts with the HERG channel at an outer pore site | Q36436477 | ||
| Structural and functional role of the extracellular s5-p linker in the HERG potassium channel | Q36436566 | ||
| Mapping the binding site of a human ether-a-go-go-related gene-specific peptide toxin (ErgTx) to the channel's outer vestibule | Q40657689 | ||
| Time course and voltage dependence of expressed HERG current compared with native "rapid" delayed rectifier K current during the cardiac ventricular action potential | Q40997568 | ||
| Allosteric effects of mutations in the extracellular S5-P loop on the gating and ion permeation properties of the hERG potassium channel | Q44867990 | ||
| P433 | issue | 43 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 42136-42148 | |
| P577 | publication date | 2003-08-05 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Structure of the HERG K+ channel S5P extracellular linker: role of an amphipathic alpha-helix in C-type inactivation | |
| P478 | volume | 278 |
| Q33155692 | A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance |
| Q28481507 | A molecular switch driving inactivation in the cardiac K+ channel HERG |
| Q89619946 | An Update on the Structure of hERG |
| Q90452449 | Anti-Ro52 antibody acts on the S5-pore linker of hERG to chronically reduce channel expression |
| Q37580457 | Delayed rectifier K(+) currents and cardiac repolarization. |
| Q45783631 | Differential effects of the β-adrenoceptor blockers carvedilol and metoprolol on SQT1- and SQT2-mutant channels |
| Q44913448 | Dynamic conformational changes of extracellular S5-P linkers in the hERG channel |
| Q82927163 | Effect of S5P alpha-helix charge mutants on inactivation of hERG K+ channels |
| Q47414764 | Functional interaction between extracellular sodium, potassium and inactivation gating in HERG channels |
| Q36445757 | Gating charges in the activation and inactivation processes of the HERG channel |
| Q37464835 | Gating the pore of potassium leak channels |
| Q35112974 | Identification of a key residue in Kv7.1 potassium channel essential for sensing external potassium ions |
| Q24299208 | Insight into the molecular interaction between the cyclic nucleotide-binding homology domain and the eag domain of the hERG channel |
| Q38007114 | Insights into hERG K+ channel structure and function from NMR studies |
| Q82951867 | Mapping the sequence of conformational changes underlying selectivity filter gating in the K(v)11.1 potassium channel |
| Q35794534 | Mechanism of block of the hERG K+ channel by the scorpion toxin CnErg1 |
| Q37068868 | Modeling HERG and its interactions with drugs: recent advances in light of current potassium channel simulations |
| Q39706375 | Molecular coupling in the human ether-a-go-go-related gene-1 (hERG1) K+ channel inactivation pathway |
| Q50660457 | Molecular mapping of a site for Cd2+-induced modification of human ether-à-go-go-related gene (hERG) channel activation. |
| Q36545039 | Molecular mechanisms for drug interactions with hERG that cause long QT syndrome. |
| Q33938901 | Open conformation of hERG channel turrets revealed by a specific scorpion toxin BmKKx2 |
| Q37464272 | Probing the binding sites and mechanisms of action of two human ether-a-go-go-related gene channel activators, 1,3-bis-(2-hydroxy-5-trifluoromethyl-phenyl)-urea (NS1643) and 2-[2-(3,4-dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic aci |
| Q35753771 | Probing the outer mouth structure of the HERG channel with peptide toxin footprinting and molecular modeling. |
| Q33634079 | Proline scan of the HERG channel S6 helix reveals the location of the intracellular pore gate. |
| Q37707953 | Rescue of mutated cardiac ion channels in inherited arrhythmia syndromes. |
| Q46145312 | Role of intracellular domains in the function of the herg potassium channel |
| Q38515325 | Selectivity filters and cysteine-rich extracellular loops in voltage-gated sodium, calcium, and NALCN channels |
| Q84631320 | Short QT syndrome |
| Q42426874 | Structural refinement of the hERG1 pore and voltage-sensing domains with ROSETTA-membrane and molecular dynamics simulations. |
| Q39648603 | Structure of the Cyclic Nucleotide-Binding Homology Domain of the hERG Channel and Its Insight into Type 2 Long QT Syndrome |
| Q33420526 | Structure of the pore-helix of the hERG K(+) channel |
| Q51810570 | Temperature dependence of human ether-a-go-go-related gene K+ currents. |
| Q41161638 | The Human Ether-a-go-go-related Gene (hERG) Potassium Channel Represents an Unusual Target for Protease-mediated Damage. |
| Q46640857 | The M1P1 loop of TASK3 K2P channels apposes the selectivity filter and influences channel function. |
| Q46256143 | The pore domain outer helix contributes to both activation and inactivation of the HERG K+ channel. |
| Q39436716 | Towards a Structural View of Drug Binding to hERG K(+) Channels |
| Q43128275 | Triazolyl azabicyclo[3.1.0]hexanes: A class of potent and selective dopamine D(3) receptor antagonists |
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