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1fyg

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</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=1fyg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1fyg OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1fyg RCSB], [http://www.ebi.ac.uk/pdbsum/1fyg PDBsum]</span></td></tr>
</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=1fyg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1fyg OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1fyg RCSB], [http://www.ebi.ac.uk/pdbsum/1fyg PDBsum]</span></td></tr>
</table>
</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/CXSO3_CONST CXSO3_CONST]] Omega-conotoxins act at presynaptic membranes, they bind and block voltage-gated calcium channels (Cav). This peptide selectively targets N-type voltage-gated calcium channels (Cav2.2/CACNA1B). Displays an analgesic potency similar to MVIIA in a range of acute and chronic pain models in rodents, but has less adverse effects compared with identical dosages of MVIIA injected intrathecally.<ref>PMID:15880145</ref>
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== References ==
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<references/>
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</StructureSection>
</StructureSection>

Revision as of 10:58, 25 December 2014

Solution structure of omega conotoxin SO3 determined by 1H-NMR

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