5cbo

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m (Protected "5cbo" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 5cbo is ON HOLD
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==Fusion protein of mbp3-16 and B4 domain of protein A from staphylococcal aureus==
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<StructureSection load='5cbo' size='340' side='right'caption='[[5cbo]], [[Resolution|resolution]] 2.80&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5cbo]] is a 12 chain structure with sequence from [https://en.wikipedia.org/wiki/Staphylococcus_aureus Staphylococcus aureus] and [https://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5CBO OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5CBO 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">X-ray diffraction, [[Resolution|Resolution]] 2.802&#8491;</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=5cbo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5cbo OCA], [https://pdbe.org/5cbo PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5cbo RCSB], [https://www.ebi.ac.uk/pdbsum/5cbo PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5cbo ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/SPA_STAAU SPA_STAAU]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Building a sophisticated protein nano-assembly requires a method for linking protein components in a predictable and stable structure. Most of the cross linkers available have flexible spacers. Because of this, the linked hybrids have significant structural flexibility and the relative structure between their two components is largely unpredictable. Here we describe a method of connecting two proteins via a 'fusion alpha helix' formed by joining two pre-existing helices into a single extended helix. Because simple ligation of two helices does not guarantee the formation of a continuous helix, we used EY-CBS, a synthetic cross linker that has been shown to react selectively with cysteines in alpha-helices, to stabilize the connecting helix. Formation and stabilization of the fusion helix was confirmed by determining the crystal structures of the fusion proteins with and without bound EY-CBS. Our method should be widely applicable for linking protein building blocks to generate predictable structures.
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Authors: Jeong, W.H., Lee, H., Song, D.H., Lee, J.O.
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Connecting two proteins using a fusion alpha helix stabilized by a chemical cross linker.,Jeong WH, Lee H, Song DH, Eom JH, Kim SC, Lee HS, Lee H, Lee JO Nat Commun. 2016 Mar 16;7:11031. doi: 10.1038/ncomms11031. PMID:26980593<ref>PMID:26980593</ref>
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Description: fusion protein of mbp3-16 and B4 domain of protein A from staphylococcal aureus
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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: Song, D.H]]
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<div class="pdbe-citations 5cbo" style="background-color:#fffaf0;"></div>
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[[Category: Lee, J.O]]
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== References ==
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[[Category: Lee, H]]
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<references/>
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[[Category: Jeong, W.H]]
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Staphylococcus aureus]]
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[[Category: Synthetic construct]]
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[[Category: Jeong WH]]
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[[Category: Lee H]]
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[[Category: Lee JO]]
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[[Category: Song DH]]

Current revision

Fusion protein of mbp3-16 and B4 domain of protein A from staphylococcal aureus

PDB ID 5cbo

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