2n86: Difference between revisions

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'''Unreleased structure'''


The entry 2n86 is ON HOLD  until Paper Publication
==NMR structure of OtTx1a - ICK==
<StructureSection load='2n86' size='340' side='right'caption='[[2n86]]' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[2n86]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Oxyopes_takobius Oxyopes takobius]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2N86 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2N86 FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR, 20 models</td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2n86 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2n86 OCA], [https://pdbe.org/2n86 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2n86 RCSB], [https://www.ebi.ac.uk/pdbsum/2n86 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2n86 ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/SPN1A_OXYTA SPN1A_OXYTA]
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
We have recently demonstrated that a common phenomenon in evolution of spider venom composition is the emergence of so-called modular toxins consisting of two domains, each corresponding to a "usual" single-domain toxin. In this article, we describe the structure of two domains that build up a modular toxin named spiderine or OtTx1a from the venom of Oxyopes takobius. Both domains were investigated by solution NMR in water and detergent micelles used to mimic membrane environment. The N-terminal spiderine domain OtTx1a-AMP (41 amino acid residues) contains no cysteines. It is disordered in aqueous solution but in micelles, it assumes a stable amphiphilic structure consisting of two alpha-helices separated by a flexible linker. On the contrary, the C-terminal domain OtTx1a-ICK (59 residues) is a disulfide-rich polypeptide reticulated by five S-S bridges. It presents a stable structure in water and its core is the inhibitor cystine knot (ICK) or knottin motif that is common among single-domain neurotoxins. OtTx1a-ICK structure is the first knottin with five disulfide bridges and it represents a good reference for the whole oxytoxin family. The affinity of both domains to membranes was measured with NMR using titration by liposome suspensions. In agreement with biological tests, OtTx1a-AMP was found to show high membrane affinity explaining its potent antimicrobial properties.


Authors: Nadezhdin, K., Romanovskaya, D., Sachkova, M., Vassilevski, A., Grishin, E., Kovalchuk, S., Arseniev, A.
Modular toxin from the lynx spider Oxyopes takobius: Structure of spiderine domains in solution and membrane-mimicking environment.,Nadezhdin KD, Romanovskaia DD, Sachkova MY, Oparin PB, Kovalchuk SI, Grishin EV, Arseniev AS, Vassilevski AA Protein Sci. 2017 Mar;26(3):611-616. doi: 10.1002/pro.3101. Epub 2017 Feb 12. PMID:27997708<ref>PMID:27997708</ref>


Description: NMR structure of OtTx1a -ICK
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
[[Category: Unreleased Structures]]
</div>
[[Category: Grishin, E]]
<div class="pdbe-citations 2n86" style="background-color:#fffaf0;"></div>
[[Category: Nadezhdin, K]]
== References ==
[[Category: Vassilevski, A]]
<references/>
[[Category: Sachkova, M]]
__TOC__
[[Category: Romanovskaya, D]]
</StructureSection>
[[Category: Arseniev, A]]
[[Category: Large Structures]]
[[Category: Kovalchuk, S]]
[[Category: Oxyopes takobius]]
[[Category: Arseniev A]]
[[Category: Grishin E]]
[[Category: Kovalchuk S]]
[[Category: Nadezhdin K]]
[[Category: Romanovskaya D]]
[[Category: Sachkova M]]
[[Category: Vassilevski A]]

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