6cnj

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'''Unreleased structure'''
 
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The entry 6cnj is ON HOLD until Paper Publication
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==Structure of the 2alpha3beta stiochiometry of the human Alpha4Beta2 nicotinic receptor==
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<StructureSection load='6cnj' size='340' side='right' caption='[[6cnj]], [[Resolution|resolution]] 3.40&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6cnj]] is a 11 chain structure with sequence from [http://en.wikipedia.org/wiki/ ] and [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6CNJ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6CNJ FirstGlance]. <br>
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Description:
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=BMA:BETA-D-MANNOSE'>BMA</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=NCT:(S)-3-(1-METHYLPYRROLIDIN-2-YL)PYRIDINE'>NCT</scene>, <scene name='pdbligand=Y01:CHOLESTEROL+HEMISUCCINATE'>Y01</scene></td></tr>
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[[Category: Unreleased Structures]]
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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=6cnj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6cnj OCA], [http://pdbe.org/6cnj PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6cnj RCSB], [http://www.ebi.ac.uk/pdbsum/6cnj PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6cnj ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[[http://www.uniprot.org/uniprot/ACHA4_HUMAN ACHA4_HUMAN]] Autosomal dominant nocturnal frontal lobe epilepsy. The disease is caused by mutations affecting the gene represented in this entry. [[http://www.uniprot.org/uniprot/ACHB2_HUMAN ACHB2_HUMAN]] Defects in CHRNB2 are the cause of nocturnal frontal lobe epilepsy type 3 (ENFL3) [MIM:[http://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>
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== Function ==
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[[http://www.uniprot.org/uniprot/ACHA4_HUMAN ACHA4_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 sodium ions.<ref>PMID:22361591</ref> [[http://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>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Mus musculus]]
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[[Category: Gharpure, A]]
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[[Category: Hibbs, R E]]
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[[Category: Jr, R W.Walsh]]
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[[Category: Morales-Perez, C L]]
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[[Category: Roh, S H]]
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[[Category: Teng, J]]
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[[Category: Acetylcholine receptor]]
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[[Category: Cys-loop receptor]]
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[[Category: Ligand-gated ion channel]]
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[[Category: Membrane protein]]
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[[Category: Transport protein]]

Revision as of 08:11, 2 May 2018

Structure of the 2alpha3beta stiochiometry of the human Alpha4Beta2 nicotinic receptor

6cnj, resolution 3.40Å

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