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4R7C

Crystal Structure of CNG mimicking NaK-ETPP mutant cocrystallized with DiMethylammonium

Summary for 4R7C
Entry DOI10.2210/pdb4r7c/pdb
Related3K0D 3K0G 4R50 4R6Z
DescriptorPotassium channel protein, GLYCINE, (4S)-2-METHYL-2,4-PENTANEDIOL, ... (5 entities in total)
Functional Keywordsalpha-helical membrane protein, nak-chimera channel in complex with dima+, transport protein
Biological sourceBacillus cereus ATCC 14579
Total number of polymer chains4
Total formula weight46873.83
Authors
De March, M.,Napolitano, L.M.R.,Onesti, S. (deposition date: 2014-08-27, release date: 2015-07-01, Last modification date: 2023-09-20)
Primary citationNapolitano, L.M.,Bisha, I.,De March, M.,Marchesi, A.,Arcangeletti, M.,Demitri, N.,Mazzolini, M.,Rodriguez, A.,Magistrato, A.,Onesti, S.,Laio, A.,Torre, V.
A structural, functional, and computational analysis suggests pore flexibility as the base for the poor selectivity of CNG channels.
Proc.Natl.Acad.Sci.USA, 112:E3619-E3628, 2015
Cited by
PubMed Abstract: Cyclic nucleotide-gated (CNG) ion channels, despite a significant homology with the highly selective K(+) channels, do not discriminate among monovalent alkali cations and are permeable also to several organic cations. We combined electrophysiology, molecular dynamics (MD) simulations, and X-ray crystallography to demonstrate that the pore of CNG channels is highly flexible. When a CNG mimic is crystallized in the presence of a variety of monovalent cations, including Na(+), Cs(+), and dimethylammonium (DMA(+)), the side chain of Glu66 in the selectivity filter shows multiple conformations and the diameter of the pore changes significantly. MD simulations indicate that Glu66 and the prolines in the outer vestibule undergo large fluctuations, which are modulated by the ionic species and the voltage. This flexibility underlies the coupling between gating and permeation and the poor ionic selectivity of CNG channels.
PubMed: 26100907
DOI: 10.1073/pnas.1503334112
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

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