2ksr
From Proteopedia
(Difference between revisions)
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==NMR structures of TM domain of the n-Acetylcholine receptor b2 subunit== | ==NMR structures of TM domain of the n-Acetylcholine receptor b2 subunit== | ||
- | <StructureSection load='2ksr' size='340' side='right' caption='[[2ksr]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> | + | <StructureSection load='2ksr' size='340' side='right'caption='[[2ksr]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> |
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[2ksr]] is a 1 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[2ksr]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2KSR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2KSR FirstGlance]. <br> |
- | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">CHRNB2 ([ | + | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">CHRNB2 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr> |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2ksr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ksr OCA], [https://pdbe.org/2ksr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2ksr RCSB], [https://www.ebi.ac.uk/pdbsum/2ksr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2ksr ProSAT]</span></td></tr> |
</table> | </table> | ||
== Disease == | == Disease == | ||
- | [[ | + | [[https://www.uniprot.org/uniprot/ACHB2_HUMAN ACHB2_HUMAN]] Defects in CHRNB2 are the cause of nocturnal frontal lobe epilepsy type 3 (ENFL3) [MIM:[https://omim.org/entry/605375 605375]]. ENFL3 is an autosomal dominant epilepsy characterized by nocturnal seizures with hyperkinetic automatisms and poorly organized stereotyped movements.<ref>PMID:11062464</ref> <ref>PMID:11104662</ref> |
== Function == | == Function == | ||
- | [[ | + | [[https://www.uniprot.org/uniprot/ACHB2_HUMAN ACHB2_HUMAN]] After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane permeable to sodiun ions.<ref>PMID:22361591</ref> |
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Human]] | [[Category: Human]] | ||
+ | [[Category: Large Structures]] | ||
[[Category: Bondarenko, V]] | [[Category: Bondarenko, V]] | ||
[[Category: Tang, P]] | [[Category: Tang, P]] |
Revision as of 07:31, 14 April 2021
NMR structures of TM domain of the n-Acetylcholine receptor b2 subunit
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Categories: Human | Large Structures | Bondarenko, V | Tang, P | Tillman, T | Xu, Y | Cell junction | Cell membrane | Disease mutation | Disulfide bond | Epilepsy | Glycoprotein | Hfip | Ion transport | Ionic channel | Membrane | Membrane protein | Nicotinic acetylcholine receptor | Polymorphism | Postsynaptic cell membrane | Synapse | Transmembrane | Transmembrane domain | Transport