2n07
From Proteopedia
(Difference between revisions)
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| - | '''Unreleased structure''' | ||
| - | + | ==Design of a Highly Stable Disulfide-Deleted Mutant of Analgesic Cyclic alpha-Conotoxin Vc1.1== | |
| - | + | <StructureSection load='2n07' size='340' side='right' caption='[[2n07]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[2n07]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2N07 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2N07 FirstGlance]. <br> | |
| - | + | </td></tr><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=2n07 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2n07 OCA], [http://pdbe.org/2n07 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2n07 RCSB], [http://www.ebi.ac.uk/pdbsum/2n07 PDBsum]</span></td></tr> | |
| - | [[Category: | + | </table> |
| - | [[Category: | + | == Function == |
| + | [[http://www.uniprot.org/uniprot/CA1A_CONVC CA1A_CONVC]] Alpha-conotoxins act on postsynaptic membranes, they bind to the nicotinic acetylcholine receptors (nAChR) and thus inhibit them. This synthetic peptide (produced without hydroxyproline, nor 4-carboxyglutamate) is a neuronal nAChR antagonist that acts as a powerful analgesic. It blocks nAChRs composed of alpha-3 or -5/beta-2 (IC(50)=7.2 uM), alpha-3/beta-2 (IC(50)=7.3 uM), alpha-3/beta-4 (IC(50)=4.2 uM), alpha-3 or -5/beta-4 (IC(50)<30 uM), alpha-4/beta-2 (IC(50)<30 uM), alpha-4/beta-4 (IC(50)<30 uM) and alpha/beta/gamma/delta (IC(50)<30 uM) subunits.<ref>PMID:12779345</ref> <ref>PMID:15770155</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Adams, D]] | ||
| + | [[Category: Akcan, M]] | ||
[[Category: Berecki, G]] | [[Category: Berecki, G]] | ||
[[Category: Craik, D]] | [[Category: Craik, D]] | ||
| + | [[Category: Jia, X]] | ||
[[Category: Kaas, Q]] | [[Category: Kaas, Q]] | ||
| + | [[Category: Seymour, V]] | ||
[[Category: Yu, R]] | [[Category: Yu, R]] | ||
| - | [[Category: | + | [[Category: Cvc1 1]] |
| - | [[Category: | + | [[Category: Disulfide-deleted mutant]] |
| - | [[Category: | + | [[Category: Toxin]] |
Revision as of 11:15, 12 May 2016
Design of a Highly Stable Disulfide-Deleted Mutant of Analgesic Cyclic alpha-Conotoxin Vc1.1
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Categories: Adams, D | Akcan, M | Berecki, G | Craik, D | Jia, X | Kaas, Q | Seymour, V | Yu, R | Cvc1 1 | Disulfide-deleted mutant | Toxin
