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2mz4

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==Solution Structure of mu-SLPTX-Ssm6a==
==Solution Structure of mu-SLPTX-Ssm6a==
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<StructureSection load='2mz4' size='340' side='right' caption='[[2mz4]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
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<StructureSection load='2mz4' size='340' side='right'caption='[[2mz4]]' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[2mz4]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MZ4 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2MZ4 FirstGlance]. <br>
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<table><tr><td colspan='2'>[[2mz4]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Scolopendra_subspinipes Scolopendra subspinipes]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MZ4 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2MZ4 FirstGlance]. <br>
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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=2mz4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mz4 OCA], [http://pdbe.org/2mz4 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2mz4 RCSB], [http://www.ebi.ac.uk/pdbsum/2mz4 PDBsum]</span></td></tr>
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</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=2mz4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mz4 OCA], [https://pdbe.org/2mz4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2mz4 RCSB], [https://www.ebi.ac.uk/pdbsum/2mz4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2mz4 ProSAT]</span></td></tr>
</table>
</table>
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== Function ==
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[https://www.uniprot.org/uniprot/TX32A_SCOMU TX32A_SCOMU] Gating-modifier toxin that inhibits voltage-gated sodium channel with a preference for hNav1.7/SCN9A (IC(50)=25.4 nM) over hNav1.1/SCN1A (IC(50)=4.1 uM), hNav1.2/SCN2A (IC(50)=813 nM), and hNav1.6/SCN8A (IC(50)=15.2 uM) (PubMed:24082113). Is an effective analgesic in rodent pain models, since it is several-fold more effective than morphine in a rodent model of formalin-induced pain and is equipotent with morphine in its ability to reduce thermal and acid-induced pain (PubMed:24082113). In addition, this peptide shows a high level of resistance to proteases and a high thermal stability that may be explained by its predominant composition of alpha-helices (PubMed:24082113).<ref>PMID:24082113</ref>
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== References ==
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<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Kim, J H]]
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[[Category: Large Structures]]
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[[Category: Kim, J I]]
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[[Category: Scolopendra subspinipes]]
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[[Category: Gating modifier]]
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[[Category: Kim JH]]
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[[Category: Mu-slptx-ssm6a]]
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[[Category: Kim JI]]
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[[Category: Sodium 1 7 channel]]
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[[Category: Toxin]]
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Current revision

Solution Structure of mu-SLPTX-Ssm6a

PDB ID 2mz4

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