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2mu8

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'''Unreleased structure'''
 
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The entry 2mu8 is ON HOLD
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==Residues belonging the n-terminal region derived of merozoite surface protein-2 of plasmodium falciparum==
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<StructureSection load='2mu8' size='340' side='right'caption='[[2mu8]]' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[2mu8]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Plasmodium_falciparum Plasmodium falciparum]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MU8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2MU8 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2mu8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mu8 OCA], [https://pdbe.org/2mu8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2mu8 RCSB], [https://www.ebi.ac.uk/pdbsum/2mu8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2mu8 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/MSA2_PLAF7 MSA2_PLAF7] May play a role in the merozoite attachment to the erythrocyte.
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The conserved, nonantigenic, nonimmunogenic malaria Merozoite Surface Protein-2 peptide 1, having high affinity for red blood cells, was rendered immunogenic and protective in Aotus monkeys by specifically changing some critical residues. The NMR structure revealed a switch from classical type III' into distorted III' and III beta turns in the protective peptides. These changes may lead to a better fit into the Aotus MHC class II human HLA-DRbeta1 12 molecule equivalent, thus activating the immune system.
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Authors: Cifuentes, G., Patarroyo, M.E., Urquiza, M., Ramirez, L.E., Reyes, C., Rodriguez, R.
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Distorting malaria peptide backbone structure to enable fitting into MHC class II molecules renders modified peptides immunogenic and protective.,Cifuentes G, Patarroyo ME, Urquiza M, Ramirez LE, Reyes C, Rodriguez R J Med Chem. 2003 May 22;46(11):2250-3. PMID:12747797<ref>PMID:12747797</ref>
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Description: Distorting malaria peptide backbone structure to enable fitting into MHC class II molecules renders modified peptides immunogenic and protective.
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 2mu8" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Plasmodium falciparum]]
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[[Category: Cifuentes G]]
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[[Category: Patarroyo ME]]
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[[Category: Ramirez LE]]
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[[Category: Reyes C]]
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[[Category: Rodriguez R]]
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[[Category: Urquiza M]]

Current revision

Residues belonging the n-terminal region derived of merozoite surface protein-2 of plasmodium falciparum

PDB ID 2mu8

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