2n0j

<div style="background-color:#fffaf0;">

== Publication Abstract from PubMed ==

To ensure appropriate metabolic regulation, riboswitches must discriminate efficiently between their target ligands and chemically similar molecules that are also present in the cell. A remarkable example of efficient ligand discrimination is a synthetic neomycin-sensing riboswitch. Paromomycin, which differs from neomycin only by the substitution of a single amino group with a hydroxy group, also binds but does not flip the riboswitch. Interestingly, the solution structures of the two riboswitch-ligand complexes are virtually identical. In this work, we demonstrate that the local loss of key intermolecular interactions at the substitution site is translated through a defined network of intramolecular interactions into global changes in RNA conformational dynamics. The remarkable specificity of this riboswitch is thus based on structural dynamics rather than static structural differences. In this respect, the neomycin riboswitch is a model for many of its natural counterparts.

What a Difference an OH Makes: Conformational Dynamics as the Basis for the Ligand Specificity of the Neomycin-Sensing Riboswitch.,Duchardt-Ferner E, Gottstein-Schmidtke SR, Weigand JE, Ohlenschlager O, Wurm JP, Hammann C, Suess B, Wohnert J Angew Chem Int Ed Engl. 2015 Dec 11. doi: 10.1002/anie.201507365. PMID:26661511<ref>PMID:26661511</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>

</div>

<div class="pdbe-citations 2n0j" style="background-color:#fffaf0;"></div>

== References ==

<references/>