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2fqn

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(New page: 200px<br /><applet load="2fqn" size="350" color="white" frame="true" align="right" spinBox="true" caption="2fqn, resolution 2.300&Aring;" /> '''Crystal structure o...)
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==Overview==
==Overview==
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The decoding A site of the small ribosomal subunit is an RNA molecular, switch, which monitors codon-anticodon interactions to guarantee, translation fidelity. We have solved the crystal structure of an RNA, fragment containing two Homo sapiens cytoplasmic A sites. Each of the two, A sites presents a different conformational state. In one state, adenines, A1492 and A1493 are fully bulged-out with C1409 forming a wobble-like pair, to A1491. In the second state, adenines A1492 and A1493 form, non-Watson-Crick pairs with C1409 and G1408, respectively while A1491, bulges out. The first state of the eukaryotic A site is, thus, basically, the same as in the bacterial A site with bulging A1492 and A1493. It is, the state used for recognition of the codon/anticodon complex. On the, contrary, the second state of the H.sapiens cytoplasmic A site is, drastically different from any of those observed for the bacterial A site, without bulging A1492 and A1493.
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The decoding A site of the small ribosomal subunit is an RNA molecular switch, which monitors codon-anticodon interactions to guarantee translation fidelity. We have solved the crystal structure of an RNA fragment containing two Homo sapiens cytoplasmic A sites. Each of the two A sites presents a different conformational state. In one state, adenines A1492 and A1493 are fully bulged-out with C1409 forming a wobble-like pair to A1491. In the second state, adenines A1492 and A1493 form non-Watson-Crick pairs with C1409 and G1408, respectively while A1491 bulges out. The first state of the eukaryotic A site is, thus, basically the same as in the bacterial A site with bulging A1492 and A1493. It is the state used for recognition of the codon/anticodon complex. On the contrary, the second state of the H.sapiens cytoplasmic A site is drastically different from any of those observed for the bacterial A site without bulging A1492 and A1493.
==About this Structure==
==About this Structure==
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[[Category: rrna]]
[[Category: rrna]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jan 29 19:42:36 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:24:09 2008''

Revision as of 15:24, 21 February 2008


2fqn, resolution 2.300Å

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Crystal structure of the Homo sapiens cytoplasmic ribosomal decoding A site

Overview

The decoding A site of the small ribosomal subunit is an RNA molecular switch, which monitors codon-anticodon interactions to guarantee translation fidelity. We have solved the crystal structure of an RNA fragment containing two Homo sapiens cytoplasmic A sites. Each of the two A sites presents a different conformational state. In one state, adenines A1492 and A1493 are fully bulged-out with C1409 forming a wobble-like pair to A1491. In the second state, adenines A1492 and A1493 form non-Watson-Crick pairs with C1409 and G1408, respectively while A1491 bulges out. The first state of the eukaryotic A site is, thus, basically the same as in the bacterial A site with bulging A1492 and A1493. It is the state used for recognition of the codon/anticodon complex. On the contrary, the second state of the H.sapiens cytoplasmic A site is drastically different from any of those observed for the bacterial A site without bulging A1492 and A1493.

About this Structure

2FQN is a Protein complex structure of sequences from [1] with and as ligands. Full crystallographic information is available from OCA.

Reference

Two conformational states in the crystal structure of the Homo sapiens cytoplasmic ribosomal decoding A site., Kondo J, Urzhumtsev A, Westhof E, Nucleic Acids Res. 2006 Feb 1;34(2):676-85. Print 2006. PMID:16452297

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