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8b1x

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Current revision (06:34, 25 January 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8b1x is ON HOLD until Paper Publication
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==Solution NMR structure of the single alpha helix peptide (P3-7)2==
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<StructureSection load='8b1x' size='340' side='right'caption='[[8b1x]]' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8b1x]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Unidentified Unidentified]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8B1X OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8B1X FirstGlance]. <br>
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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=8b1x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8b1x OCA], [https://pdbe.org/8b1x PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8b1x RCSB], [https://www.ebi.ac.uk/pdbsum/8b1x PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8b1x ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The binding of intrinsically disordered proteins to globular ones can require the folding of motifs into alpha-helices. These interactions offer opportunities for therapeutic intervention but their modulation with small molecules is challenging because they bury large surfaces. Linear peptides that display the residues that are key for binding can be targeted to globular proteins when they form stable helices, which in most cases requires their chemical modification. Here we present rules to design peptides that fold into single alpha-helices by instead concatenating glutamine side chain to main chain hydrogen bonds recently discovered in polyglutamine helices. The resulting peptides are uncharged, contain only natural amino acids, and their sequences can be optimized to interact with specific targets. Our results provide design rules to obtain single alpha-helices for a wide range of applications in protein engineering and drug design.
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Authors: Escobedo, A., Coles, M., Diercks, T., Garcia, J., Millet, O., Salvatella, X.
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A glutamine-based single alpha-helix scaffold to target globular proteins.,Escobedo A, Piccirillo J, Aranda J, Diercks T, Mateos B, Garcia-Cabau C, Sanchez-Navarro M, Topal B, Biesaga M, Staby L, Kragelund BB, Garcia J, Millet O, Orozco M, Coles M, Crehuet R, Salvatella X Nat Commun. 2022 Nov 18;13(1):7073. doi: 10.1038/s41467-022-34793-6. PMID:36400768<ref>PMID:36400768</ref>
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Description: Solution NMR structure of the single alpha helix peptide (P3-7)2
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Salvatella, X]]
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<div class="pdbe-citations 8b1x" style="background-color:#fffaf0;"></div>
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[[Category: Millet, O]]
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== References ==
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[[Category: Garcia, J]]
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<references/>
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[[Category: Escobedo, A]]
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__TOC__
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[[Category: Diercks, T]]
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</StructureSection>
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[[Category: Coles, M]]
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[[Category: Large Structures]]
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[[Category: Unidentified]]
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[[Category: Coles M]]
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[[Category: Diercks T]]
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[[Category: Escobedo A]]
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[[Category: Garcia J]]
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[[Category: Millet O]]
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[[Category: Salvatella X]]

Current revision

Solution NMR structure of the single alpha helix peptide (P3-7)2

PDB ID 8b1x

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