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2ro2

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(New page: '''Unreleased structure''' The entry 2ro2 is ON HOLD until Paper Publication Authors: Gallego, J., Dufour, D., Gago, S., De la Pena, M., Flores, R. Description: Solution structure of d...)
Current revision (12:54, 20 December 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 2ro2 is ON HOLD until Paper Publication
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==Solution structure of domain I of the negative polarity CChMVd hammerhead ribozyme==
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<StructureSection load='2ro2' size='340' side='right'caption='[[2ro2]]' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[2ro2]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2RO2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2RO2 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">Solution NMR</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=2ro2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ro2 OCA], [https://pdbe.org/2ro2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2ro2 RCSB], [https://www.ebi.ac.uk/pdbsum/2ro2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2ro2 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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Loop-loop tertiary interactions play a key role in the folding and catalytic activity of natural hammerhead ribozymes. Using a combination of NMR spectroscopy, site-directed mutagenesis and kinetic and infectivity analyses, we have examined the structure and function of loops 1 and 2 of the (+) and (-) hammerheads of chrysanthemum chlorotic mottle viroid RNA. In both hammerheads, loop 1 is a heptanucleotide hairpin loop containing an exposed U at its 5' side and an extrahelical U at its 3'-side critical for the catalytic activity of the ribozyme in vitro and for viroid infectivity in vivo, whereas loop 2 has a key opened A at its 3'-side. These structural features promote a specific loop-loop interaction motif across the major groove. The essential features of this tertiary structure element, base pairing between the 5' U of loop 1 and the 3' A of loop 2, and interaction of the extrahelical pyrimidine of loop 1 with loop 2, are likely shared by a significant fraction of natural hammerheads.
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Authors: Gallego, J., Dufour, D., Gago, S., De la Pena, M., Flores, R.
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Structure-function analysis of the ribozymes of chrysanthemum chlorotic mottle viroid: a loop-loop interaction motif conserved in most natural hammerheads.,Dufour D, de la Pena M, Gago S, Flores R, Gallego J Nucleic Acids Res. 2008 Nov 29. PMID:19043070<ref>PMID:19043070</ref>
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Description: Solution structure of domain I of the negative polarity CChMVd hammerhead ribozyme
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 2ro2" style="background-color:#fffaf0;"></div>
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==See Also==
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jun 11 08:49:40 2008''
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*[[Ribozyme 3D structures|Ribozyme 3D structures]]
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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: Large Structures]]
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[[Category: Dufour D]]
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[[Category: Flores R]]
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[[Category: Gago S]]
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[[Category: Gallego J]]
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[[Category: De la Pena M]]

Current revision

Solution structure of domain I of the negative polarity CChMVd hammerhead ribozyme

PDB ID 2ro2

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