Literature DB >> 15835891

Comparison of the global structure and dynamics of native and unmodified tRNAval.

Annaleen Vermeulen1, Scott A McCallum, Arthur Pardi.   

Abstract

The effects of post-transcriptional modifications on the structure and dynamics of Escherichia coli tRNA(val) were studied by NMR spectroscopy. NMR chemical shift data and residual dipolar couplings were used to show that the local secondary and tertiary structures are very similar in native and unmodified tRNA(val). Rigid body restrained molecular dynamics calculations showed that the global structure of tRNA is unchanged by the post-transcriptional modifications. Deuterium exchange NMR experiments were used to probe the dynamics and flexibility of native and unmodified tRNA(val). A similar set of slowly exchanging (t(1/2) > 3 min) imino protons were observed in both tRNAs, but the rates of exchange for the slowest exchanging imino protons were approximately 20 times faster in unmodified than in native tRNA. These results demonstrate that the dynamics and flexibility of tRNA(val), but not the local or global structure, are significantly affected by post-transcriptional modifications.

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Year:  2005        PMID: 15835891     DOI: 10.1021/bi0473399

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  28 in total

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2.  Comparison of alignment tensors generated for native tRNA(Val) using magnetic fields and liquid crystalline media.

Authors:  Michael P Latham; Paul Hanson; Darin J Brown; Arthur Pardi
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Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2005-07-30

4.  Magnetic field induced residual dipolar couplings of imino groups in nucleic acids from measurements at a single magnetic field.

Authors:  Jinfa Ying; Alexander Grishaev; Michael P Latham; Arthur Pardi; Ad Bax
Journal:  J Biomol NMR       Date:  2007-08-07       Impact factor: 2.835

Review 5.  Kinetic barriers and the role of topology in protein and RNA folding.

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Journal:  Protein Sci       Date:  2008-05-23       Impact factor: 6.725

6.  Tuning the affinity of aminoacyl-tRNA to elongation factor Tu for optimal decoding.

Authors:  Jared M Schrader; Stephen J Chapman; Olke C Uhlenbeck
Journal:  Proc Natl Acad Sci U S A       Date:  2011-03-14       Impact factor: 11.205

7.  The La protein functions redundantly with tRNA modification enzymes to ensure tRNA structural stability.

Authors:  Laura A Copela; Ghadiyaram Chakshusmathi; R Lynn Sherrer; Sandra L Wolin
Journal:  RNA       Date:  2006-04       Impact factor: 4.942

8.  Crystal structure of Streptococcus pneumoniae Sp1610, a putative tRNA methyltransferase, in complex with S-adenosyl-L-methionine.

Authors:  Hai Minh Ta; Kyeong Kyu Kim
Journal:  Protein Sci       Date:  2010-03       Impact factor: 6.725

9.  The crystal structure of unmodified tRNAPhe from Escherichia coli.

Authors:  Robert T Byrne; Andrey L Konevega; Marina V Rodnina; Alfred A Antson
Journal:  Nucleic Acids Res       Date:  2010-03-04       Impact factor: 16.971

10.  Direct observation of the temperature-induced melting process of the Salmonella fourU RNA thermometer at base-pair resolution.

Authors:  Jörg Rinnenthal; Birgit Klinkert; Franz Narberhaus; Harald Schwalbe
Journal:  Nucleic Acids Res       Date:  2010-03-07       Impact factor: 16.971

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