Literature DB >> 21474301

Emerging structural themes in large RNA molecules.

Nicholas J Reiter1, Clarence W Chan, Alfonso Mondragón.   

Abstract

Extensive networks of tertiary interactions give rise to unique, highly organized domain architectures that characterize the three-dimensional structure of large RNA molecules. Formed by stacked layers of a near-planar arrangement of contiguous coaxial helices, large RNA molecules are relatively flat in overall shape. The functional core of these molecules is stabilized by a diverse set of tertiary interaction motifs that often bring together distant regions of conserved nucleotides. Although homologous RNAs from different organisms can be structurally diverse, they adopt a structurally conserved functional core that includes preassembled active and/or substrate binding sites. These findings broaden our understanding of RNA folding and tertiary structure stabilization, illustrating how large, complex RNAs assemble into unique structures to perform recognition and catalysis.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21474301      PMCID: PMC3112254          DOI: 10.1016/j.sbi.2011.03.003

Source DB:  PubMed          Journal:  Curr Opin Struct Biol        ISSN: 0959-440X            Impact factor:   6.809


  50 in total

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5.  Basis for structural diversity in homologous RNAs.

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  16 in total

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Review 4.  Hierarchy of RNA functional dynamics.

Authors:  Anthony M Mustoe; Charles L Brooks; Hashim M Al-Hashimi
Journal:  Annu Rev Biochem       Date:  2014-03-05       Impact factor: 23.643

5.  3dRNAscore: a distance and torsion angle dependent evaluation function of 3D RNA structures.

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7.  Structural Roles of Noncoding RNAs in the Heart of Enzymatic Complexes.

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Review 8.  Structure and function of the T-loop structural motif in noncoding RNAs.

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10.  The bacterial ribonuclease P holoenzyme requires specific, conserved residues for efficient catalysis and substrate positioning.

Authors:  Nicholas J Reiter; Amy K Osterman; Alfonso Mondragón
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