1rnk

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(New page: 200px<br /><applet load="1rnk" size="450" color="white" frame="true" align="right" spinBox="true" caption="1rnk" /> '''THE STRUCTURE OF AN RNA PSEUDOKNOT THAT CAUS...)
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'''THE STRUCTURE OF AN RNA PSEUDOKNOT THAT CAUSES EFFICIENT FRAMESHIFTING IN MOUSE MAMMARY TUMOR VIRUS'''<br />
'''THE STRUCTURE OF AN RNA PSEUDOKNOT THAT CAUSES EFFICIENT FRAMESHIFTING IN MOUSE MAMMARY TUMOR VIRUS'''<br />
==Overview==
==Overview==
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The structure of a 34-nucleotide RNA pseudoknot that causes efficient -1, frameshifting in the messenger RNA of mouse mammary tumor virus has been, investigated by NMR. Spectral assignment of the pseudoknot was facilitated, by comparative NMR studies on the pseudoknot and on two smaller hairpin, RNAs, and by using selective 13C labeling and 13C-edited NMR techniques., The three-dimensional structure of the pseudoknot has been determined. The, frameshifter pseudoknot possesses structural features not observed in, previously reported model pseudoknots. It has a compact structure with a, pronounced bend at the junction of its G.C-rich stems. A single adenylate, residue is intercalated between the two stems so that direct coaxial, staking of the stems is not possible. The lack of an opposing nucleotide, for the stacked, intervening adenylate creates a hinge in the pseudoknot., Most of the loop nucleotides are restrained by base staking interactions, which keep the loops from adopting extended conformations. The sterically, constrained loops direct the bending of the pseudoknot at the stem-stem, junction. The roles of the intercalated adenylate and loop lengths in, causing bending can explain their requirement for efficient frameshifting., Our NMR data also indicate that there are internal dynamics associated, with the pseudoknot. The unique, compact structure and conformational, flexibility of the pseudoknot may be required for recognition and, favourable interaction with the translating ribosome, or with translation, factors associated with the ribosome.
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The structure of a 34-nucleotide RNA pseudoknot that causes efficient -1 frameshifting in the messenger RNA of mouse mammary tumor virus has been investigated by NMR. Spectral assignment of the pseudoknot was facilitated by comparative NMR studies on the pseudoknot and on two smaller hairpin RNAs, and by using selective 13C labeling and 13C-edited NMR techniques. The three-dimensional structure of the pseudoknot has been determined. The frameshifter pseudoknot possesses structural features not observed in previously reported model pseudoknots. It has a compact structure with a pronounced bend at the junction of its G.C-rich stems. A single adenylate residue is intercalated between the two stems so that direct coaxial staking of the stems is not possible. The lack of an opposing nucleotide for the stacked, intervening adenylate creates a hinge in the pseudoknot. Most of the loop nucleotides are restrained by base staking interactions which keep the loops from adopting extended conformations. The sterically constrained loops direct the bending of the pseudoknot at the stem-stem junction. The roles of the intercalated adenylate and loop lengths in causing bending can explain their requirement for efficient frameshifting. Our NMR data also indicate that there are internal dynamics associated with the pseudoknot. The unique, compact structure and conformational flexibility of the pseudoknot may be required for recognition and favourable interaction with the translating ribosome, or with translation factors associated with the ribosome.
==About this Structure==
==About this Structure==
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1RNK is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1RNK OCA].
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1RNK is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1RNK OCA].
==Reference==
==Reference==
The structure of an RNA pseudoknot that causes efficient frameshifting in mouse mammary tumor virus., Shen LX, Tinoco I Jr, J Mol Biol. 1995 Apr 14;247(5):963-78. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=7723043 7723043]
The structure of an RNA pseudoknot that causes efficient frameshifting in mouse mammary tumor virus., Shen LX, Tinoco I Jr, J Mol Biol. 1995 Apr 14;247(5):963-78. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=7723043 7723043]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Junior, I.Tinoco.]]
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[[Category: Junior, I Tinoco.]]
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[[Category: Shen, L.X.]]
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[[Category: Shen, L X.]]
[[Category: mouse mammary tumor virus]]
[[Category: mouse mammary tumor virus]]
[[Category: nmr]]
[[Category: nmr]]
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[[Category: rna]]
[[Category: rna]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sat Nov 24 22:59:12 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:52:42 2008''

Revision as of 12:52, 21 February 2008


1rnk

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THE STRUCTURE OF AN RNA PSEUDOKNOT THAT CAUSES EFFICIENT FRAMESHIFTING IN MOUSE MAMMARY TUMOR VIRUS

Overview

The structure of a 34-nucleotide RNA pseudoknot that causes efficient -1 frameshifting in the messenger RNA of mouse mammary tumor virus has been investigated by NMR. Spectral assignment of the pseudoknot was facilitated by comparative NMR studies on the pseudoknot and on two smaller hairpin RNAs, and by using selective 13C labeling and 13C-edited NMR techniques. The three-dimensional structure of the pseudoknot has been determined. The frameshifter pseudoknot possesses structural features not observed in previously reported model pseudoknots. It has a compact structure with a pronounced bend at the junction of its G.C-rich stems. A single adenylate residue is intercalated between the two stems so that direct coaxial staking of the stems is not possible. The lack of an opposing nucleotide for the stacked, intervening adenylate creates a hinge in the pseudoknot. Most of the loop nucleotides are restrained by base staking interactions which keep the loops from adopting extended conformations. The sterically constrained loops direct the bending of the pseudoknot at the stem-stem junction. The roles of the intercalated adenylate and loop lengths in causing bending can explain their requirement for efficient frameshifting. Our NMR data also indicate that there are internal dynamics associated with the pseudoknot. The unique, compact structure and conformational flexibility of the pseudoknot may be required for recognition and favourable interaction with the translating ribosome, or with translation factors associated with the ribosome.

About this Structure

1RNK is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

The structure of an RNA pseudoknot that causes efficient frameshifting in mouse mammary tumor virus., Shen LX, Tinoco I Jr, J Mol Biol. 1995 Apr 14;247(5):963-78. PMID:7723043

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