2iz8: Difference between revisions
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New page: left|200px<br /><applet load="2iz8" size="450" color="white" frame="true" align="right" spinBox="true" caption="2iz8, resolution 3.30Å" /> '''MS2-RNA HAIRPIN (C-7... |
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[[Image:2iz8.gif|left|200px]]<br /><applet load="2iz8" size=" | [[Image:2iz8.gif|left|200px]]<br /><applet load="2iz8" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="2iz8, resolution 3.30Å" /> | caption="2iz8, resolution 3.30Å" /> | ||
'''MS2-RNA HAIRPIN (C-7) COMPLEX'''<br /> | '''MS2-RNA HAIRPIN (C-7) COMPLEX'''<br /> | ||
==Overview== | ==Overview== | ||
We have determined the structures of complexes between the phage MS2 coat | We have determined the structures of complexes between the phage MS2 coat protein and variants of the replicase translational operator in order to explore the sequence specificity of the RNA-protein interaction. The 19-nt RNA hairpins studied have substitutions at two positions that have been shown to be important for specific binding. At one of these positions, -10, which is a bulged adenosine (A) in the stem of the wild-type operator hairpin, substitutions were made with guanosine (G), cytidine (C) and two non-native bases, 2-aminopurine (2AP) and inosine (I). At the other position, -7 in the hairpin loop, the native adenine was substituted with a cytidine. Of these, only the G-10, C-10 and C-7 variants showed interpretable density for the RNA hairpin. In spite of large differences in binding affinities, the structures of the variant complexes are very similar to the wild-type operator complex. For G-10 substitutions in hairpin variants that can form bulges at alternative places in the stem, the binding affinity is low and a partly disordered conformation is seen in the electron density maps. The affinity is similar to that of wild-type when the base pairs adjacent to the bulged nucleotide are selected to avoid alternative conformations. Both purines bind in a very similar way in a pocket in the protein. In the C-10 variant, which has very low affinity, the cytidine is partly inserted in the protein pocket rather than intercalated in the RNA stem. Substitution of the wild-type adenosine at position -7 by pyrimidines gives strongly reduced affinities, but the structure of the C-7 complex shows that the base occupies the same position as the A-7 in the wild-type RNA. It is stacked in the RNA and makes no direct contact with the protein. | ||
==About this Structure== | ==About this Structure== | ||
2IZ8 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Enterobacterio_phage_ms2 Enterobacterio phage ms2]. This structure | 2IZ8 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Enterobacterio_phage_ms2 Enterobacterio phage ms2]. This structure supersedes the now removed PDB entry 1GKV. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2IZ8 OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Helgstrand, C.]] | [[Category: Helgstrand, C.]] | ||
[[Category: Liljas, L.]] | [[Category: Liljas, L.]] | ||
[[Category: Stockley, P | [[Category: Stockley, P G.]] | ||
[[Category: Stonehouse, N | [[Category: Stonehouse, N J.]] | ||
[[Category: capsid]] | [[Category: capsid]] | ||
[[Category: complex (capsid protein/rna hairpin)]] | [[Category: complex (capsid protein/rna hairpin)]] | ||
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[[Category: virus]] | [[Category: virus]] | ||
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