2n8d

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==In silico designed antimicrobial peptide Lavracin==
==In silico designed antimicrobial peptide Lavracin==
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<StructureSection load='2n8d' size='340' side='right'caption='[[2n8d]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
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<StructureSection load='2n8d' size='340' side='right'caption='[[2n8d]]' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[2n8d]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2N8D OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2N8D FirstGlance]. <br>
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<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2N8D OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2N8D FirstGlance]. <br>
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</td></tr><tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=NH2:AMINO+GROUP'>NH2</scene></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=2n8d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2n8d OCA], [https://pdbe.org/2n8d PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2n8d RCSB], [https://www.ebi.ac.uk/pdbsum/2n8d PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2n8d ProSAT]</span></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=2n8d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2n8d OCA], [https://pdbe.org/2n8d PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2n8d RCSB], [https://www.ebi.ac.uk/pdbsum/2n8d PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2n8d ProSAT]</span></td></tr>
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</table>
</table>
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<div style="background-color:#fffaf0;">
 
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== Publication Abstract from PubMed ==
 
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Specific interactions of peptides with lipid membranes are essential for cellular communication and constitute a central aspect of the innate host defense against pathogens. A computational method for generating innovative membrane-pore-forming peptides inspired by natural templates is presented. Peptide representation in terms of sequence- and topology-dependent hydrophobic moments is introduced. This design concept proves to be appropriate for the de novo generation of first-in-class membrane-active peptides with the anticipated mode of action. The designed peptides outperform the natural template in terms of their antibacterial activity. They form a kinked helical structure and self-assemble in the membrane by an entropy-driven mechanism to form dynamically growing pores that are dependent on the lipid composition. The results of this study demonstrate the unique potential of natural template-based peptide design for chemical biology and medicinal chemistry.
 
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Rational Design of Membrane-Pore-Forming Peptides.,Pillong M, Hiss JA, Schneider P, Lin YC, Posselt G, Pfeiffer B, Blatter M, Muller AT, Bachler S, Neuhaus CS, Dittrich PS, Altmann KH, Wessler S, Schneider G Small. 2017 Aug 11. doi: 10.1002/smll.201701316. PMID:28799716<ref>PMID:28799716</ref>
 
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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 2n8d" style="background-color:#fffaf0;"></div>
 
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== References ==
 
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<references/>
 
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Blatter, M]]
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[[Category: Blatter M]]
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[[Category: Pillong, M]]
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[[Category: Pillong M]]
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[[Category: Schneider, G]]
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[[Category: Schneider G]]
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[[Category: Antimicrobial peptide]]
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[[Category: De novo protein]]
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Revision as of 10:24, 31 August 2022

In silico designed antimicrobial peptide Lavracin

PDB ID 2n8d

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