2gyb

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(New page: 200px<br /><applet load="2gyb" size="450" color="white" frame="true" align="right" spinBox="true" caption="2gyb" /> '''Structure of the 30S subunit of a SecM-stall...)
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[[Image:2gyb.gif|left|200px]]<br /><applet load="2gyb" size="350" color="white" frame="true" align="right" spinBox="true"
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'''Structure of the 30S subunit of a SecM-stalled E. coli ribosome complex obtained by fitting atomic models for RNA and protein components into cryo-EM map EMD-1143'''<br />
'''Structure of the 30S subunit of a SecM-stalled E. coli ribosome complex obtained by fitting atomic models for RNA and protein components into cryo-EM map EMD-1143'''<br />
==Overview==
==Overview==
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In E. coli, the SecM nascent polypeptide causes elongation arrest, while, interacting with 23S RNA bases A2058 and A749-753 in the exit tunnel of, the large ribosomal subunit. We compared atomic models fitted by, real-space refinement into cryo-electron microscopy reconstructions of a, pretranslocational and SecM-stalled E. coli ribosome complex. A cascade of, RNA rearrangements propagates from the exit tunnel throughout the large, subunit, affecting intersubunit bridges and tRNA positions, which in turn, reorient small subunit RNA elements. Elongation arrest could result from, the inhibition of mRNA.(tRNAs) translocation, E site tRNA egress, and, perhaps translation factor activation at the GTPase-associated center. Our, study suggests that the specific secondary and tertiary arrangement of, ribosomal RNA provides the basis for internal signal transduction within, the ribosome. Thus, the ribosome may itself have the ability to regulate, its progression through translation by modulating its structure and, consequently its receptivity to activation by cofactors.
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In E. coli, the SecM nascent polypeptide causes elongation arrest, while interacting with 23S RNA bases A2058 and A749-753 in the exit tunnel of the large ribosomal subunit. We compared atomic models fitted by real-space refinement into cryo-electron microscopy reconstructions of a pretranslocational and SecM-stalled E. coli ribosome complex. A cascade of RNA rearrangements propagates from the exit tunnel throughout the large subunit, affecting intersubunit bridges and tRNA positions, which in turn reorient small subunit RNA elements. Elongation arrest could result from the inhibition of mRNA.(tRNAs) translocation, E site tRNA egress, and perhaps translation factor activation at the GTPase-associated center. Our study suggests that the specific secondary and tertiary arrangement of ribosomal RNA provides the basis for internal signal transduction within the ribosome. Thus, the ribosome may itself have the ability to regulate its progression through translation by modulating its structure and consequently its receptivity to activation by cofactors.
==About this Structure==
==About this Structure==
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2GYB is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2GYB OCA].
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2GYB is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2GYB OCA].
==Reference==
==Reference==
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[[Category: secm; nascent chain; signal transduction; rna world; polypeptide exit tunnel; translocation; ribosome; elongation arrest; protein-conducting channel]]
[[Category: secm; nascent chain; signal transduction; rna world; polypeptide exit tunnel; translocation; ribosome; elongation arrest; protein-conducting channel]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 11:27:07 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:36:21 2008''

Revision as of 15:36, 21 February 2008


2gyb

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Structure of the 30S subunit of a SecM-stalled E. coli ribosome complex obtained by fitting atomic models for RNA and protein components into cryo-EM map EMD-1143

Overview

In E. coli, the SecM nascent polypeptide causes elongation arrest, while interacting with 23S RNA bases A2058 and A749-753 in the exit tunnel of the large ribosomal subunit. We compared atomic models fitted by real-space refinement into cryo-electron microscopy reconstructions of a pretranslocational and SecM-stalled E. coli ribosome complex. A cascade of RNA rearrangements propagates from the exit tunnel throughout the large subunit, affecting intersubunit bridges and tRNA positions, which in turn reorient small subunit RNA elements. Elongation arrest could result from the inhibition of mRNA.(tRNAs) translocation, E site tRNA egress, and perhaps translation factor activation at the GTPase-associated center. Our study suggests that the specific secondary and tertiary arrangement of ribosomal RNA provides the basis for internal signal transduction within the ribosome. Thus, the ribosome may itself have the ability to regulate its progression through translation by modulating its structure and consequently its receptivity to activation by cofactors.

About this Structure

2GYB is a Protein complex structure of sequences from Escherichia coli. Full crystallographic information is available from OCA.

Reference

Elongation arrest by SecM via a cascade of ribosomal RNA rearrangements., Mitra K, Schaffitzel C, Fabiola F, Chapman MS, Ban N, Frank J, Mol Cell. 2006 May 19;22(4):533-43. PMID:16713583

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