2mnc
From Proteopedia
(Difference between revisions)
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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=2mnc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mnc OCA], [https://pdbe.org/2mnc PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2mnc RCSB], [https://www.ebi.ac.uk/pdbsum/2mnc PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2mnc ProSAT]</span></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=2mnc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mnc OCA], [https://pdbe.org/2mnc PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2mnc RCSB], [https://www.ebi.ac.uk/pdbsum/2mnc PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2mnc ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| - | <div style="background-color:#fffaf0;"> | ||
| - | == Publication Abstract from PubMed == | ||
| - | We have used NMR spectroscopy to characterize an oligonucleotide stem loop structure based on the pre-element of an oncogenic microRNA, miR-21. This predicted stem-loop structure is cleaved from the precursor of miR-21 (pre-miR-21) by the nuclease Dicer. It is also a critical feature recognized by the protein complex that converts the primary transcript (pri-miR-21) into the pre-miRNA. The secondary structure of the native sequence is poorly defined by NMR due to rapid exchange of imino protons with solvent; however, replacement of two adjacent putative G*U base pairs with G*C base pairs retains the conformation of the hairpin observed by chemical probing and stabilizes it sufficiently to observe most of the imino proton resonances of the molecule. The observed resonances are consistent with the predicted secondary structure. In addition, a peak due to a loop uridine suggests an interaction between it and a bulged uridine in the stem. Assignment of non-exchangeable proton resonances and characterization of NOEs and coupling constants allows inference of the following features of the structure: extrahelicity of a bulged adenosine, deviation from A-form geometry in a base-paired stem, and consecutive stacking of the adenosines in the 5' side of the loop, the guanosine of the closing base pair, and a cross-strand adenosine. Modeling of the structure by restrained molecular dynamics suggests a basis for the interaction between the loop uridine, the bulged uridine in the stem, and an A*U base pair in the stem. | ||
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| - | NMR Characterization of an Oligonucleotide Model of the MiR-21 Pre-Element.,Chirayil S, Wu Q, Amezcua C, Luebke KJ PLoS One. 2014 Sep 24;9(9):e108231. doi: 10.1371/journal.pone.0108231., eCollection 2014. PMID:25250627<ref>PMID:25250627</ref> | ||
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| - | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
| - | </div> | ||
| - | <div class="pdbe-citations 2mnc" style="background-color:#fffaf0;"></div> | ||
| - | == References == | ||
| - | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
Current revision
oligonucleotide model of miR-21 pre-element
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