8UEC
Structure of TREK-1CG*:CAT335a
Summary for 8UEC
Entry DOI | 10.2210/pdb8uec/pdb |
Related | 8UE2 8UE9 |
Descriptor | Potassium channel subfamily K member 2, N-((E,2S,3R)-1,3-DIHYDROXYOCTADEC-4-EN-2-YL)PALMITAMIDE, DECANE, ... (7 entities in total) |
Functional Keywords | membrane preotein, ml335, trek1, trek-1, malemide, trek-1 ligand, crystal, trans-membrane protein, transmembrane protein, k2p, two pore potassium channel, potassium channel, kcnk2, potassium channel subfamily k member 2, membrane protein, cat335a |
Biological source | Mus musculus (house mouse) |
Total number of polymer chains | 2 |
Total formula weight | 67253.37 |
Authors | Mondal, A.,Lee, H.,Minor, D.L. (deposition date: 2023-09-30, release date: 2024-06-26, Last modification date: 2025-01-08) |
Primary citation | Deal, P.E.,Lee, H.,Mondal, A.,Lolicato, M.,Mendonca, P.R.F.,Black, H.,Jang, S.,El-Hilali, X.,Bryant, C.,Isacoff, E.Y.,Renslo, A.R.,Minor Jr., D.L. Development of covalent chemogenetic K 2P channel activators. Cell Chem Biol, 31:1305-1323.e9, 2024 Cited by PubMed Abstract: K potassium channels regulate excitability by affecting cellular resting membrane potential in the brain, cardiovascular system, immune cells, and sensory organs. Despite their important roles in anesthesia, arrhythmia, pain, hypertension, sleep, and migraine, the ability to control K function remains limited. Here, we describe a chemogenetic strategy termed CATKLAMP (covalent activation of TREK family K channels to clamp membrane potential) that leverages the discovery of a K modulator pocket site that reacts with electrophile-bearing derivatives of a TREK subfamily small-molecule activator, ML335, to activate the channel irreversibly. We show that CATKLAMP can be used to probe fundamental aspects of K function, as a switch to silence neuronal firing, and is applicable to all TREK subfamily members. Together, our findings exemplify a means to alter K channel activity that should facilitate molecular and systems level studies of K function and enable the search for new K modulators. PubMed: 39029456DOI: 10.1016/j.chembiol.2024.06.006 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3 Å) |
Structure validation
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