5kh8

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'''Unreleased structure'''
 
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The entry 5kh8 is ON HOLD until Dec 17 2018
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==Solution structures of the apo state fluoride riboswitch==
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<StructureSection load='5kh8' size='340' side='right' caption='[[5kh8]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5kh8]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5KH8 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5KH8 FirstGlance]. <br>
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</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=5kh8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5kh8 OCA], [http://pdbe.org/5kh8 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5kh8 RCSB], [http://www.ebi.ac.uk/pdbsum/5kh8 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5kh8 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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Riboswitches control gene expression through ligand-dependent structural rearrangements of the sensing aptamer domain. However, we found that the Bacillus cereus fluoride riboswitch aptamer adopts identical tertiary structures in solution with and without ligand. Using chemical-exchange saturation transfer (CEST) NMR spectroscopy, we revealed that the structured ligand-free aptamer transiently accesses a low-populated ( approximately 1%) and short-lived ( approximately 3 ms) excited conformational state that unravels a conserved 'linchpin' base pair to signal transcription termination. Upon fluoride binding, this highly localized, fleeting process is allosterically suppressed, which activates transcription. We demonstrated that this mechanism confers effective fluoride-dependent gene activation over a wide range of transcription rates, which is essential for robust toxicity responses across diverse cellular conditions. These results unveil a novel switching mechanism that employs ligand-dependent suppression of an aptamer excited state to coordinate regulatory conformational transitions rather than adopting distinct aptamer ground-state tertiary architectures, exemplifying a new mode of ligand-dependent RNA regulation.
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Authors:
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An excited state underlies gene regulation of a transcriptional riboswitch.,Zhao B, Guffy SL, Williams B, Zhang Q Nat Chem Biol. 2017 Jul 17. doi: 10.1038/nchembio.2427. PMID:28719589<ref>PMID:28719589</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 5kh8" 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: Zhang, Q]]
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[[Category: Zhao, B]]
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[[Category: Apo state]]
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[[Category: Pseudoknot]]
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[[Category: Riboswitch aptamer]]
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[[Category: Rna]]
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[[Category: Transcriptional regulation]]

Revision as of 03:51, 4 August 2017

Solution structures of the apo state fluoride riboswitch

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