2mfx: Difference between revisions

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'''Unreleased structure'''
{{STRUCTURE_2mfx|  PDB=2mfx  |  SCENE=  }}
===Non-reducible analogues of alpha-conotoxin Vc1.1: [2,8]-cis dicarba Vc1.1===
{{ABSTRACT_PUBMED_23768016}}


The entry 2mfx is ON HOLD
==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> 


Authors: Robinson, S.D., Macraild, C.A., Van Lierop, B.J., Robinson, A.J., Norton, R.S.
==About this Structure==
[[2mfx]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MFX OCA].  


Description: Non-reducible analogues of alpha-conotoxin Vc1.1: [2,8]-cis dicarba Vc1.1
==Reference==
<ref group="xtra">PMID:023768016</ref><references group="xtra"/><references/>
[[Category: Lierop, B J.Van.]]
[[Category: Macraild, C A.]]
[[Category: Norton, R S.]]
[[Category: Robinson, A J.]]
[[Category: Robinson, S D.]]
[[Category: Dicarba]]
[[Category: Toxin]]

Revision as of 13:21, 18 December 2013

Template:STRUCTURE 2mfx

Non-reducible analogues of alpha-conotoxin Vc1.1: [2,8]-cis dicarba Vc1.1Non-reducible analogues of alpha-conotoxin Vc1.1: [2,8]-cis dicarba Vc1.1

Template:ABSTRACT PUBMED 23768016

FunctionFunction

[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.[1] [2]

About this StructureAbout this Structure

2mfx is a 1 chain structure. Full experimental information is available from OCA.

ReferenceReference

[xtra 1]

  1. van Lierop BJ, Robinson SD, Kompella SN, Belgi A, McArthur JR, Hung A, MacRaild CA, Adams DJ, Norton RS, Robinson AJ. Dicarba alpha-conotoxin Vc1.1 analogues with differential selectivity for nicotinic acetylcholine and GABAB receptors. ACS Chem Biol. 2013 Aug 16;8(8):1815-21. doi: 10.1021/cb4002393. Epub 2013 Jun, 17. PMID:23768016 doi:http://dx.doi.org/10.1021/cb4002393
  1. Sandall DW, Satkunanathan N, Keays DA, Polidano MA, Liping X, Pham V, Down JG, Khalil Z, Livett BG, Gayler KR. A novel alpha-conotoxin identified by gene sequencing is active in suppressing the vascular response to selective stimulation of sensory nerves in vivo. Biochemistry. 2003 Jun 10;42(22):6904-11. PMID:12779345 doi:http://dx.doi.org/10.1021/bi034043e
  2. Lang PM, Burgstahler R, Haberberger RV, Sippel W, Grafe P. A conus peptide blocks nicotinic receptors of unmyelinated axons in human nerves. Neuroreport. 2005 Apr 4;16(5):479-83. PMID:15770155

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