1rim
From Proteopedia
(Difference between revisions)
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==E6-binding zinc finger (E6apc2)== | ==E6-binding zinc finger (E6apc2)== | ||
- | <StructureSection load='1rim' size='340' side='right'caption='[[1rim | + | <StructureSection load='1rim' size='340' side='right'caption='[[1rim]]' scene=''> |
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1rim]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1RIM OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1RIM FirstGlance]. <br> | <table><tr><td colspan='2'>[[1rim]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1RIM OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1RIM FirstGlance]. <br> | ||
- | </td></tr><tr id=' | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</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=1rim FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1rim OCA], [https://pdbe.org/1rim PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1rim RCSB], [https://www.ebi.ac.uk/pdbsum/1rim PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1rim ProSAT]</span></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=1rim FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1rim OCA], [https://pdbe.org/1rim PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1rim RCSB], [https://www.ebi.ac.uk/pdbsum/1rim PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1rim ProSAT]</span></td></tr> | ||
</table> | </table> | ||
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</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1rim ConSurf]. | </jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1rim ConSurf]. | ||
<div style="clear:both"></div> | <div style="clear:both"></div> | ||
- | <div style="background-color:#fffaf0;"> | ||
- | == Publication Abstract from PubMed == | ||
- | The E6 protein from HPV type 16 binds proteins containing a seven-residue leucine-containing motif. Previous work demonstrated that peptides containing the consensus sequence are a mixture of alpha-helix and unstructured conformations. To design monomeric E6-binding peptides that are stable in aqueous solution, we used a protein grafting approach where the critical residues of the E6-binding motif of E6-associated protein, E6AP, LQELLGE, were incorporated into exposed helices of two stably folded peptide scaffolds. One series was built using the third zinc finger of the Sp1 protein, which contains a C-terminal helix. A second series was built using a Trp-cage scaffold, which contains an N-terminal helix. The chimeric peptides had very different activities in out-competing the E6-E6AP interaction. We characterized the peptides by circular dichroism spectroscopy and determined high-resolution structures by NMR methods. The E6-binding consensus motif was found to be helical in the high-quality structures, which had backbone root-mean-square deviations of less than 0.4 A. We have successfully grafted the E6-binding motif into two parent peptides to create ligands that have biological activity while preserving the stable, native fold of their scaffolds. The data also indicate that conformational change is common in E6-binding proteins during the formation of the complex with the viral E6 protein. | ||
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- | Design and characterization of helical peptides that inhibit the E6 protein of papillomavirus.,Liu Y, Liu Z, Androphy E, Chen J, Baleja JD Biochemistry. 2004 Jun 15;43(23):7421-31. PMID:15182185<ref>PMID:15182185</ref> | ||
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- | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
- | </div> | ||
- | <div class="pdbe-citations 1rim" style="background-color:#fffaf0;"></div> | ||
- | == References == | ||
- | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | [[Category: Androphy | + | [[Category: Androphy E]] |
- | [[Category: Baleja | + | [[Category: Baleja JD]] |
- | [[Category: Chen | + | [[Category: Chen J]] |
- | [[Category: Liu | + | [[Category: Liu Y]] |
- | [[Category: Liu | + | [[Category: Liu Z]] |
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Revision as of 08:24, 1 May 2024
E6-binding zinc finger (E6apc2)
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Categories: Large Structures | Androphy E | Baleja JD | Chen J | Liu Y | Liu Z