6v5a | pdb_00006v5a

Crystal structure of the human BK channel gating ring L390P mutant

spinqualitylabelsall models 6v5a, resolution 2.00Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 6v5a is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 2Å Ligands: CA, SO4 Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function KCMA1_HUMAN Publication Abstract from PubMed Large-conductance Ca(2+) and voltage-activated K(+) (BK) channels control membrane excitability in many cell types. BK channels are tetrameric. Each subunit is composed of a voltage sensor domain (VSD), a central pore-gate domain, and a large cytoplasmic domain (CTD) that contains the Ca(2+) sensors. While it is known that BK channels are activated by voltage and Ca(2+), and that voltage and Ca(2+) activations interact, less is known about the mechanisms involved. We explore here these mechanisms by examining the gating contribution of an interface formed between the VSDs and the alphaB helices located at the top of the CTDs. Proline mutations in the alphaB helix greatly decreased voltage activation while having negligible effects on gating currents. Analysis with the Horrigan, Cui, and Aldrich model indicated a decreased coupling between voltage sensors and pore gate. Proline mutations decreased Ca(2+) activation for both Ca(2+) bowl and RCK1 Ca(2+) sites, suggesting that both high-affinity Ca(2+) sites transduce their effect, at least in part, through the alphaB helix. Mg(2+) activation also decreased. The crystal structure of the CTD with proline mutation L390P showed a flattening of the first helical turn in the alphaB helix compared to wild type, without other notable differences in the CTD, indicating that structural changes from the mutation were confined to the alphaB helix. These findings indicate that an intact alphaB helix/VSD interface is required for effective coupling of Ca(2+) binding and voltage depolarization to pore opening and that shared Ca(2+) and voltage transduction pathways involving the alphaB helix may be involved. Coupling of Ca(2+) and voltage activation in BK channels through the alphaB helix/voltage sensor interface.,Geng Y, Deng Z, Zhang G, Budelli G, Butler A, Yuan P, Cui J, Salkoff L, Magleby KL Proc Natl Acad Sci U S A. 2020 Jun 23;117(25):14512-14521. doi:, 10.1073/pnas.1908183117. Epub 2020 Jun 8. PMID:32513714 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See Also Potassium channel 3D structures

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