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1kpd

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(New page: 200px<br /><applet load="1kpd" size="450" color="white" frame="true" align="right" spinBox="true" caption="1kpd" /> '''A MUTANT RNA PSEUDOKNOT THAT PROMOTES RIBOSO...)
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'''A MUTANT RNA PSEUDOKNOT THAT PROMOTES RIBOSOMAL FRAMESHIFTING IN MOUSE MAMMARY TUMOR VIRUS, NMR, MINIMIZED AVERAGE STRUCTURE'''<br />
'''A MUTANT RNA PSEUDOKNOT THAT PROMOTES RIBOSOMAL FRAMESHIFTING IN MOUSE MAMMARY TUMOR VIRUS, NMR, MINIMIZED AVERAGE STRUCTURE'''<br />
==Overview==
==Overview==
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A single A--&gt;G mutation that changes a potential A.U base pair to a G.U, pair at the junction of the stems and loops of a non-frameshifting, pseudoknot dramatically increases its frameshifting efficiency in mouse, mammary tumor virus. The structure of the non-frameshifting pseudoknot APK, has been found to be very different from that of pseudoknots that cause, efficient frameshifting [Kang,H., Hines,J.V. and Tinoco,I. (1995) J. Mol., Biol. , 259, 135-147]. The 3-dimensional structure of the mutant, pseudoknot was determined by restrained molecular dynamics based on, NMR-derived interproton distance and torsion angle constraints. One, striking feature of the mutant pseudoknot compared with the parent, pseudoknot is that a G.U base pair forms at the top of stem 2, thus, leaving only 1 nt at the junction of the two stems. The conformation is, very different from that of the previously determined non-frameshifting, parent pseudoknot, which lacks the A.U base pair at the top of the stem, and has 2 nt between the stems. However, the conformation is quite similar, to that of efficient frameshifting pseudoknots whose structures were, previously determined by NMR. A single adenylate residue intervenes, between the two stems and interrupts their coaxial stacking. This unpaired, nucleotide produces a bent structure. The structural similarity among the, efficient frameshifting pseudoknots indicates that a specific conformation, is required for ribosomal frameshifting, further implying a specific, interaction of the pseudoknot with the ribosome.
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A single A--&gt;G mutation that changes a potential A.U base pair to a G.U pair at the junction of the stems and loops of a non-frameshifting pseudoknot dramatically increases its frameshifting efficiency in mouse mammary tumor virus. The structure of the non-frameshifting pseudoknot APK has been found to be very different from that of pseudoknots that cause efficient frameshifting [Kang,H., Hines,J.V. and Tinoco,I. (1995) J. Mol. Biol. , 259, 135-147]. The 3-dimensional structure of the mutant pseudoknot was determined by restrained molecular dynamics based on NMR-derived interproton distance and torsion angle constraints. One striking feature of the mutant pseudoknot compared with the parent pseudoknot is that a G.U base pair forms at the top of stem 2, thus leaving only 1 nt at the junction of the two stems. The conformation is very different from that of the previously determined non-frameshifting parent pseudoknot, which lacks the A.U base pair at the top of the stem and has 2 nt between the stems. However, the conformation is quite similar to that of efficient frameshifting pseudoknots whose structures were previously determined by NMR. A single adenylate residue intervenes between the two stems and interrupts their coaxial stacking. This unpaired nucleotide produces a bent structure. The structural similarity among the efficient frameshifting pseudoknots indicates that a specific conformation is required for ribosomal frameshifting, further implying a specific interaction of the pseudoknot with the ribosome.
==About this Structure==
==About this Structure==
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1KPD 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=1KPD OCA].
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1KPD 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=1KPD OCA].
==Reference==
==Reference==
A mutant RNA pseudoknot that promotes ribosomal frameshifting in mouse mammary tumor virus., Kang H, Tinoco I Jr, Nucleic Acids Res. 1997 May 15;25(10):1943-9. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=9115361 9115361]
A mutant RNA pseudoknot that promotes ribosomal frameshifting in mouse mammary tumor virus., Kang H, Tinoco I Jr, Nucleic Acids Res. 1997 May 15;25(10):1943-9. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=9115361 9115361]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Junior, I.Tinoco.]]
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[[Category: Junior, I Tinoco.]]
[[Category: Kang, H.]]
[[Category: Kang, H.]]
[[Category: ribonucleic acid]]
[[Category: ribonucleic acid]]
[[Category: rna pseudoknot]]
[[Category: rna pseudoknot]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 01:43:15 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:36:36 2008''

Revision as of 11:36, 21 February 2008


1kpd

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A MUTANT RNA PSEUDOKNOT THAT PROMOTES RIBOSOMAL FRAMESHIFTING IN MOUSE MAMMARY TUMOR VIRUS, NMR, MINIMIZED AVERAGE STRUCTURE

Overview

A single A-->G mutation that changes a potential A.U base pair to a G.U pair at the junction of the stems and loops of a non-frameshifting pseudoknot dramatically increases its frameshifting efficiency in mouse mammary tumor virus. The structure of the non-frameshifting pseudoknot APK has been found to be very different from that of pseudoknots that cause efficient frameshifting [Kang,H., Hines,J.V. and Tinoco,I. (1995) J. Mol. Biol. , 259, 135-147]. The 3-dimensional structure of the mutant pseudoknot was determined by restrained molecular dynamics based on NMR-derived interproton distance and torsion angle constraints. One striking feature of the mutant pseudoknot compared with the parent pseudoknot is that a G.U base pair forms at the top of stem 2, thus leaving only 1 nt at the junction of the two stems. The conformation is very different from that of the previously determined non-frameshifting parent pseudoknot, which lacks the A.U base pair at the top of the stem and has 2 nt between the stems. However, the conformation is quite similar to that of efficient frameshifting pseudoknots whose structures were previously determined by NMR. A single adenylate residue intervenes between the two stems and interrupts their coaxial stacking. This unpaired nucleotide produces a bent structure. The structural similarity among the efficient frameshifting pseudoknots indicates that a specific conformation is required for ribosomal frameshifting, further implying a specific interaction of the pseudoknot with the ribosome.

About this Structure

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

Reference

A mutant RNA pseudoknot that promotes ribosomal frameshifting in mouse mammary tumor virus., Kang H, Tinoco I Jr, Nucleic Acids Res. 1997 May 15;25(10):1943-9. PMID:9115361

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