22be: Difference between revisions

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'''Unreleased structure'''


The entry 22be is ON HOLD  until Paper Publication
==XEN1101 bound KCNQ2/3 heteromer with 3:1 stoichiometry, state 1==
 
<StructureSection load='22be' size='340' side='right'caption='[[22be]], [[Resolution|resolution]] 2.60&Aring;' scene=''>
Authors: Lu, F., Fan, X., Huang, J.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[22be]] is a 4 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=22BE OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=22BE FirstGlance]. <br>
Description: XEN1101 bound KCNQ2/3 heteromer with 3:1 stoichiometry, state 1
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.6&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1EY8:~{N}-[4-(6-fluoranyl-3,4-dihydro-1~{H}-isoquinolin-2-yl)-2,6-dimethyl-phenyl]-3,3-dimethyl-butanamide'>A1EY8</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</scene></td></tr>
[[Category: Fan, X]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=22be FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=22be OCA], [https://pdbe.org/22be PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=22be RCSB], [https://www.ebi.ac.uk/pdbsum/22be PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=22be ProSAT]</span></td></tr>
[[Category: Huang, J]]
</table>
[[Category: Lu, F]]
== Disease ==
[https://www.uniprot.org/uniprot/KCNQ3_HUMAN KCNQ3_HUMAN] Benign familial infantile epilepsy;Benign familial neonatal seizures;Juvenile myoclonic epilepsy. The disease is caused by mutations affecting the gene represented in this entry.  Defects in KCNQ3 may be involved in epileptic disorders. These are characterized by paroxysmal transient disturbances of the electrical activity of the brain that may be manifested as episodic impairment or loss of consciousness, abnormal motor phenomena, psychic or sensory disturbances, or perturbation of the autonomic nervous system.<ref>PMID:22612257</ref>
== Function ==
[https://www.uniprot.org/uniprot/KCNQ3_HUMAN KCNQ3_HUMAN] Probably important in the regulation of neuronal excitability. Associates with KCNQ2 or KCNQ5 to form a potassium channel with essentially identical properties to the channel underlying the native M-current, a slowly activating and deactivating potassium conductance which plays a critical role in determining the subthreshold electrical excitability of neurons as well as the responsiveness to synaptic inputs.
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Fan X]]
[[Category: Huang J]]
[[Category: Lu F]]
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