6e9e

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'''Unreleased structure'''
 
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The entry 6e9e is ON HOLD until Paper Publication
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==EsCas13d-crRNA binary complex==
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<StructureSection load='6e9e' size='340' side='right' caption='[[6e9e]], [[Resolution|resolution]] 3.40&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6e9e]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6E9E OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6E9E FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr>
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<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=6e9e FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6e9e OCA], [http://pdbe.org/6e9e PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6e9e RCSB], [http://www.ebi.ac.uk/pdbsum/6e9e PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6e9e 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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CRISPR-Cas endonucleases directed against foreign nucleic acids mediate prokaryotic adaptive immunity and have been tailored for broad genetic engineering applications. Type VI-D CRISPR systems contain the smallest known family of single effector Cas enzymes, and their signature Cas13d ribonuclease employs guide RNAs to cleave matching target RNAs. To understand the molecular basis for Cas13d function and explain its compact molecular architecture, we resolved cryoelectron microscopy structures of Cas13d-guide RNA binary complex and Cas13d-guide-target RNA ternary complex to 3.4 and 3.3 A resolution, respectively. Furthermore, a 6.5 A reconstruction of apo Cas13d combined with hydrogen-deuterium exchange revealed conformational dynamics that have implications for RNA scanning. These structures, together with biochemical and cellular characterization, provide insights into its RNA-guided, RNA-targeting mechanism and delineate a blueprint for the rational design of improved transcriptome engineering technologies.
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Authors: Zhang, C., Lyumkis, D.
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Structural Basis for the RNA-Guided Ribonuclease Activity of CRISPR-Cas13d.,Zhang C, Konermann S, Brideau NJ, Lotfy P, Wu X, Novick SJ, Strutzenberg T, Griffin PR, Hsu PD, Lyumkis D Cell. 2018 Sep 20;175(1):212-223.e17. doi: 10.1016/j.cell.2018.09.001. PMID:30241607<ref>PMID:30241607</ref>
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Description: EsCas13d-crRNA binary complex
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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: Zhang, C]]
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<div class="pdbe-citations 6e9e" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
[[Category: Lyumkis, D]]
[[Category: Lyumkis, D]]
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[[Category: Zhang, C]]
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[[Category: Complex]]
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[[Category: Crispr-ca]]
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[[Category: Rna binding protein-rna complex]]
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[[Category: Rnase]]

Revision as of 07:49, 3 October 2018

EsCas13d-crRNA binary complex

6e9e, resolution 3.40Å

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