5hs0
From Proteopedia
(Difference between revisions)
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| - | '''Unreleased structure''' | ||
| - | + | ==Computationally Designed Cyclic Tetramer ank1C4_7== | |
| + | <StructureSection load='5hs0' size='340' side='right' caption='[[5hs0]], [[Resolution|resolution]] 2.40Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[5hs0]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5HS0 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5HS0 FirstGlance]. <br> | ||
| + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | ||
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5hs0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5hs0 OCA], [http://pdbe.org/5hs0 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5hs0 RCSB], [http://www.ebi.ac.uk/pdbsum/5hs0 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5hs0 ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | Self-assembling cyclic protein homo-oligomers play important roles in biology, and the ability to generate custom homo-oligomeric structures could enable new approaches to probe biological function. Here we report a general approach to design cyclic homo-oligomers that employs a new residue-pair-transform method to assess the designability of a protein-protein interface. This method is sufficiently rapid to enable the systematic enumeration of cyclically docked arrangements of a monomer followed by sequence design of the newly formed interfaces. We use this method to design interfaces onto idealized repeat proteins that direct their assembly into complexes that possess cyclic symmetry. Of 96 designs that were characterized experimentally, 21 were found to form stable monodisperse homo-oligomers in solution, and 15 (four homodimers, six homotrimers, six homotetramers and one homopentamer) had solution small-angle X-ray scattering data consistent with the design models. X-ray crystal structures were obtained for five of the designs and each is very close to their corresponding computational model. | ||
| - | + | Computational design of self-assembling cyclic protein homo-oligomers.,Fallas JA, Ueda G, Sheffler W, Nguyen V, McNamara DE, Sankaran B, Pereira JH, Parmeggiani F, Brunette TJ, Cascio D, Yeates TR, Zwart P, Baker D Nat Chem. 2017 Apr;9(4):353-360. doi: 10.1038/nchem.2673. Epub 2016 Dec 5. PMID:28338692<ref>PMID:28338692</ref> | |
| - | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
| - | + | </div> | |
| + | <div class="pdbe-citations 5hs0" style="background-color:#fffaf0;"></div> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
[[Category: Baker, D]] | [[Category: Baker, D]] | ||
| - | [[Category: Mcnamara, D.E]] | ||
| - | [[Category: Yeates, T.O]] | ||
| - | [[Category: Fallas, J.A]] | ||
[[Category: Cascio, D]] | [[Category: Cascio, D]] | ||
| + | [[Category: Fallas, J A]] | ||
| + | [[Category: McNamara, D E]] | ||
| + | [[Category: Yeates, T O]] | ||
| + | [[Category: De novo protein]] | ||
| + | [[Category: Designed oligomeric interface]] | ||
| + | [[Category: Protein design]] | ||
Revision as of 11:37, 12 April 2017
Computationally Designed Cyclic Tetramer ank1C4_7
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