24vu: Difference between revisions

Line 1:

~~'''Unreleased structure'''~~

~~The entry~~ 24vu is ~~ON HOLD~~

==Cryo-EM structure of the human KCNQ2/KCNQ3 heterotetramer (2:2 stoichiometry) with CLM142 (M2233 CLM142, with symmetry expansion)==

~~Authors~~: ~~Wang~~, Y.F., ~~Yang~~, H., Qu, Y.N., ~~Shen~~, H.Z.

== Structural highlights ==

<table><tr><td colspan='2'>[[24vu]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Aequorea_victoria Aequorea victoria] and [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=24VU OCA]. For a guided tour on the structure components use [https://proteopedia.org/fgij/fg.htm?mol=24VU FirstGlance].

~~Description~~: ~~Cryo-EM structure~~ of the ~~human KCNQ2~~/~~KCNQ3 heterotetramer (2~~:~~2 stoichiometry)~~ with ~~CLM142 (M2233 CLM142~~, ~~with symmetry expansion)~~

</td></tr><tr id='method'><td class="sblockLbl">[[Empirical_models|Method:]]</td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.68Å</td></tr>

[[Category: ~~Unreleased~~ Structures]]

<tr id='ligand'><td class="sblockLbl">[[Ligand|Ligands:]]</td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=9PE:(1R)-2-{[(S)-(2-AMINOETHOXY)(HYDROXY)PHOSPHORYL]OXY}-1-[(HEPTANOYLOXY)METHYL]ETHYL+OCTADECANOATE'>9PE</scene>, <scene name='pdbligand=A1E7E:~{N}-(7-cyclopropyl-1-prop-2-ynyl-indazol-3-yl)-4-fluoranyl-benzamide'>A1E7E</scene>, <scene name='pdbligand=YJ0:(2~{R},3~{S},4~{S},5~{R},6~{R})-2-(hydroxymethyl)-6-[(2~{R},3~{S},4~{R},5~{R},6~{R})-2-(hydroxymethyl)-6-[2-[[(2~{R},3~{R},4~{R},5~{S},6~{R})-6-(hydroxymethyl)-5-[6-(hydroxymethyl)-3,4,5-tris(oxidanyl)oxan-2-yl]oxy-3,4-bis(oxidanyl)oxan-2-yl]oxymethyl]-4-[(1~{S},2~{S},4~{S},5~{R},6~{R},7~{S},8~{R},9~{S},12~{S},13~{R},16~{S})-5,7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icos-18-ene-6,2-oxane]-16-yl]oxy-butoxy]-4,5-bis(oxidanyl)oxan-3-yl]oxy-oxane-3,4,5-triol'>YJ0</scene></td></tr>

[[Category: ~~Wang, Y.F~~]]

<tr id='resources'><td class="sblockLbl">Resources:</td><td class="sblockDat">[https://proteopedia.org/fgij/fg.htm?mol=24vu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=24vu OCA], [https://pdbe.org/24vu PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=24vu RCSB], [https://www.ebi.ac.uk/pdbsum/24vu PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=24vu ProSAT]</td></tr>

[[Category: Shen~~, H.Z~~]]

</table>

[[Category: ~~Yang, H~~]]

== Disease ==

[[Category: ~~Qu, Y.N~~]]

[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 ==

__TOC__

</StructureSection>

[[Category: Aequorea victoria]]

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Qu YN]]

[[Category: Shen HZ]]

[[Category: Wang YF]]

[[Category: Yang H]]

Navigation menu

Page actions

Page actions

Personal tools

Navigation

Search

Tools

@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 24vu is ON HOLD
+==Cryo-EM structure of the human KCNQ2/KCNQ3 heterotetramer (2:2 stoichiometry) with CLM142 (M2233 CLM142, with symmetry expansion)==
+<StructureSection load='24vu' size='340' side='right'caption='[[24vu]], [[Resolution|resolution]] 3.68&Aring;' scene=''>
-Authors: Wang, Y.F., Yang, H., Qu, Y.N., Shen, H.Z.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[24vu]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Aequorea_victoria Aequorea victoria] and [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=24VU OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=24VU FirstGlance]. <br>
-Description: Cryo-EM structure of the human KCNQ2/KCNQ3 heterotetramer (2:2 stoichiometry) with CLM142 (M2233 CLM142, with symmetry expansion)
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.68&#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=9PE:(1R)-2-{[(S)-(2-AMINOETHOXY)(HYDROXY)PHOSPHORYL]OXY}-1-[(HEPTANOYLOXY)METHYL]ETHYL+OCTADECANOATE'>9PE</scene>, <scene name='pdbligand=A1E7E:~{N}-(7-cyclopropyl-1-prop-2-ynyl-indazol-3-yl)-4-fluoranyl-benzamide'>A1E7E</scene>, <scene name='pdbligand=YJ0:(2~{R},3~{S},4~{S},5~{R},6~{R})-2-(hydroxymethyl)-6-[(2~{R},3~{S},4~{R},5~{R},6~{R})-2-(hydroxymethyl)-6-[2-[[(2~{R},3~{R},4~{R},5~{S},6~{R})-6-(hydroxymethyl)-5-[6-(hydroxymethyl)-3,4,5-tris(oxidanyl)oxan-2-yl]oxy-3,4-bis(oxidanyl)oxan-2-yl]oxymethyl]-4-[(1~{S},2~{S},4~{S},5~{R},6~{R},7~{S},8~{R},9~{S},12~{S},13~{R},16~{S})-5,7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icos-18-ene-6,2-oxane]-16-yl]oxy-butoxy]-4,5-bis(oxidanyl)oxan-3-yl]oxy-oxane-3,4,5-triol'>YJ0</scene></td></tr>
-[[Category: Wang, Y.F]]
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=24vu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=24vu OCA], [https://pdbe.org/24vu PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=24vu RCSB], [https://www.ebi.ac.uk/pdbsum/24vu PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=24vu ProSAT]</span></td></tr>
-[[Category: Shen, H.Z]]
+</table>
-[[Category: Yang, H]]
+== Disease ==
-[[Category: Qu, Y.N]]
+[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: Aequorea victoria]]
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Qu YN]]
+[[Category: Shen HZ]]
+[[Category: Wang YF]]
+[[Category: Yang H]]