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| | ==Human K2P4.1 (TRAAAK) potassium channel, W262S mutant== | | ==Human K2P4.1 (TRAAAK) potassium channel, W262S mutant== |
| - | <StructureSection load='4ruf' size='340' side='right' caption='[[4ruf]], [[Resolution|resolution]] 3.40Å' scene=''> | + | <StructureSection load='4ruf' size='340' side='right'caption='[[4ruf]], [[Resolution|resolution]] 3.40Å' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[4ruf]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4RUF OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4RUF FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[4ruf]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4RUF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4RUF FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=K:POTASSIUM+ION'>K</scene></td></tr> | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=K:POTASSIUM+ION'>K</scene></td></tr> |
| - | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4rue|4rue]]</td></tr>
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4ruf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4ruf OCA], [https://pdbe.org/4ruf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4ruf RCSB], [https://www.ebi.ac.uk/pdbsum/4ruf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4ruf ProSAT]</span></td></tr> |
| - | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">KCNK4, TRAAK ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>
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| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4ruf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4ruf OCA], [http://pdbe.org/4ruf PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4ruf RCSB], [http://www.ebi.ac.uk/pdbsum/4ruf PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4ruf ProSAT]</span></td></tr> | + | |
| | </table> | | </table> |
| | == Function == | | == Function == |
| - | [[http://www.uniprot.org/uniprot/KCNK4_HUMAN KCNK4_HUMAN]] Voltage insensitive, instantaneous, outwardly rectifying potassium channel. Outward rectification is reversed at high external K(+) concentrations (By similarity). | + | [https://www.uniprot.org/uniprot/KCNK4_HUMAN KCNK4_HUMAN] Voltage insensitive, instantaneous, outwardly rectifying potassium channel. Outward rectification is reversed at high external K(+) concentrations (By similarity). |
| | <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| | == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| | </div> | | </div> |
| | <div class="pdbe-citations 4ruf" style="background-color:#fffaf0;"></div> | | <div class="pdbe-citations 4ruf" style="background-color:#fffaf0;"></div> |
| | + | |
| | + | ==See Also== |
| | + | *[[Potassium channel 3D structures|Potassium channel 3D structures]] |
| | == References == | | == References == |
| | <references/> | | <references/> |
| | __TOC__ | | __TOC__ |
| | </StructureSection> | | </StructureSection> |
| - | [[Category: Human]] | + | [[Category: Homo sapiens]] |
| - | [[Category: Lolicato, M]] | + | [[Category: Large Structures]] |
| - | [[Category: Minor, D L.Jr]] | + | [[Category: Lolicato M]] |
| - | [[Category: Metal transport]] | + | [[Category: Minor DLJr]] |
| - | [[Category: Traak potassium ion channel]]
| + | |
| Structural highlights
Function
KCNK4_HUMAN Voltage insensitive, instantaneous, outwardly rectifying potassium channel. Outward rectification is reversed at high external K(+) concentrations (By similarity).
Publication Abstract from PubMed
Mechanical and thermal activation of ion channels is central to touch, thermosensation, and pain. The TRAAK/TREK K2P potassium channel subfamily produces background currents that alter neuronal excitability in response to pressure, temperature, signaling lipids, and anesthetics. How such diverse stimuli control channel function is unclear. Here we report structures of K2P4.1 (TRAAK) bearing C-type gate-activating mutations that reveal a tilting and straightening of the M4 inner transmembrane helix and a buckling of the M2 transmembrane helix. These conformational changes move M4 in a direction opposite to that in classical potassium channel activation mechanisms and open a passage lateral to the pore that faces the lipid bilayer inner leaflet. Together, our findings uncover a unique aspect of K2P modulation, indicate a means for how the K2P C-terminal cytoplasmic domain affects the C-type gate which lies approximately 40A away, and suggest how lipids and bilayer inner leaflet deformations may gate the channel.
Transmembrane Helix Straightening and Buckling Underlies Activation of Mechanosensitive and Thermosensitive K2P Channels.,Lolicato M, Riegelhaupt PM, Arrigoni C, Clark KA, Minor DL Jr Neuron. 2014 Dec 17;84(6):1198-212. doi: 10.1016/j.neuron.2014.11.017. Epub 2014 , Dec 11. PMID:25500157[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Lolicato M, Riegelhaupt PM, Arrigoni C, Clark KA, Minor DL Jr. Transmembrane Helix Straightening and Buckling Underlies Activation of Mechanosensitive and Thermosensitive K2P Channels. Neuron. 2014 Dec 17;84(6):1198-212. doi: 10.1016/j.neuron.2014.11.017. Epub 2014 , Dec 11. PMID:25500157 doi:http://dx.doi.org/10.1016/j.neuron.2014.11.017
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