1z2j

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[[Image:1z2j.gif|left|200px]]<br /><applet load="1z2j" size="350" color="white" frame="true" align="right" spinBox="true"
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[[Image:1z2j.gif|left|200px]]
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caption="1z2j" />
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'''Solution structure of the HIV-1 frameshift inducing element'''<br />
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{{Structure
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|PDB= 1z2j |SIZE=350|CAPTION= <scene name='initialview01'>1z2j</scene>
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|SITE=
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|LIGAND=
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|ACTIVITY=
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|GENE=
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}}
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'''Solution structure of the HIV-1 frameshift inducing element'''
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==Overview==
==Overview==
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==About this Structure==
==About this Structure==
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1Z2J 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=1Z2J OCA].
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1Z2J is a [[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=1Z2J OCA].
==Reference==
==Reference==
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Solution structure and thermodynamic investigation of the HIV-1 frameshift inducing element., Staple DW, Butcher SE, J Mol Biol. 2005 Jun 24;349(5):1011-23. Epub 2005 Apr 1. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15927637 15927637]
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Solution structure and thermodynamic investigation of the HIV-1 frameshift inducing element., Staple DW, Butcher SE, J Mol Biol. 2005 Jun 24;349(5):1011-23. Epub 2005 Apr 1. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15927637 15927637]
[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Butcher, S E.]]
[[Category: Butcher, S E.]]
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[[Category: tetraloop]]
[[Category: tetraloop]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:11:29 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 15:30:28 2008''

Revision as of 13:30, 20 March 2008


PDB ID 1z2j

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Coordinates: save as pdb, mmCIF, xml



Solution structure of the HIV-1 frameshift inducing element


Overview

Expression of the HIV reverse transcriptase and other essential viral enzymes requires a -1 translational frameshift. The frameshift event is induced by two highly conserved RNA elements within the HIV-1 mRNA: a UUUUUUA heptamer known as the slippery sequence, and a downstream RNA structure. Here, we report structural and thermodynamic evidence that the HIV-1 frameshift site RNA forms a stem-loop and lower helix separated by a three-purine bulge. We have determined the structure of the 45 nucleotide frameshift site RNA using multidimensional heteronuclear nuclear magnetic resonance (NMR) methods. The upper helix is highly thermostable (T(m)>90 degrees C), forming 11 Watson-Crick base-pairs capped by a stable ACAA tetraloop. The eight base-pair lower helix was found to be only moderately stable (T(m)=47 degrees C). A three-purine bulge separates the highly stable upper helix from the lower helix. Base stacking in the bulge forms a wedge, introducing a 60 degrees bend between the helices. Interestingly, this bend is similar to those seen in a number of frameshift inducing pseudoknots for which structures have been solved. The lower helix must denature to allow the ribosome access to the slippery site, but likely functions as a positioning element that enhances frameshift efficiency.

About this Structure

1Z2J is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

Solution structure and thermodynamic investigation of the HIV-1 frameshift inducing element., Staple DW, Butcher SE, J Mol Biol. 2005 Jun 24;349(5):1011-23. Epub 2005 Apr 1. PMID:15927637

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