7u5d

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'''Unreleased structure'''
 
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The entry 7u5d is ON HOLD until Paper Publication
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==I-F3b Cascade-TniQ full R-loop complex==
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<StructureSection load='7u5d' size='340' side='right'caption='[[7u5d]], [[Resolution|resolution]] 3.52&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7u5d]] is a 13 chain structure with sequence from [https://en.wikipedia.org/wiki/Aeromonas_salmonicida Aeromonas salmonicida]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7U5D OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7U5D 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=7u5d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7u5d OCA], [https://pdbe.org/7u5d PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7u5d RCSB], [https://www.ebi.ac.uk/pdbsum/7u5d PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7u5d 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-associated transposons (CASTs) are natural RNA-directed transposition systems. We demonstrate that transposon protein TniQ plays a central role in promoting R-loop formation by RNA-guided DNA-targeting modules. TniQ residues, proximal to CRISPR RNA (crRNA), are required for recognizing different crRNA categories, revealing an unappreciated role of TniQ to direct transposition into different classes of crRNA targets. To investigate adaptations allowing CAST elements to utilize attachment sites inaccessible to CRISPR-Cas surveillance complexes, we compared and contrasted PAM sequence requirements in both I-F3b CAST and I-F1 CRISPR-Cas systems. We identify specific amino acids that enable a wider range of PAM sequences to be accommodated in I-F3b CAST elements compared with I-F1 CRISPR-Cas, enabling CAST elements to access attachment sites as sequences drift and evade host surveillance. Together, this evidence points to the central role of TniQ in facilitating the acquisition of CRISPR effector complexes for RNA-guided DNA transposition.
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Authors:
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Multiple adaptations underly co-option of a CRISPR surveillance complex for RNA-guided DNA transposition.,Park JU, Petassi MT, Hsieh SC, Mehrotra E, Schuler G, Budhathoki J, Truong VH, Thyme SB, Ke A, Kellogg EH, Peters JE Mol Cell. 2023 Jun 1;83(11):1827-1838.e6. doi: 10.1016/j.molcel.2023.05.005. PMID:37267904<ref>PMID:37267904</ref>
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Description:
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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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<div class="pdbe-citations 7u5d" 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>
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[[Category: Aeromonas salmonicida]]
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[[Category: Large Structures]]
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[[Category: Kellogg EH]]
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[[Category: Mehrotra E]]
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[[Category: Park JU]]

Revision as of 09:35, 21 June 2023

I-F3b Cascade-TniQ full R-loop complex

PDB ID 7u5d

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