2qbi

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(New page: 200px<br /><applet load="2qbi" size="350" color="white" frame="true" align="right" spinBox="true" caption="2qbi, resolution 4.0&Aring;" /> '''Crystal structure of ...)
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==Overview==
==Overview==
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Aminoglycosides are widely used antibiotics that cause messenger RNA, decoding errors, block mRNA and transfer RNA translocation, and inhibit, ribosome recycling. Ribosome recycling follows the termination of protein, synthesis and is aided by ribosome recycling factor (RRF) in bacteria. The, molecular mechanism by which aminoglycosides inhibit ribosome recycling is, unknown. Here we show in X-ray crystal structures of the Escherichia coli, 70S ribosome that RRF binding causes RNA helix H69 of the large ribosomal, subunit, which is crucial for subunit association, to swing away from the, subunit interface. Aminoglycosides bind to H69 and completely restore the, contacts between ribosomal subunits that are disrupted by RRF. These, results provide a structural explanation for aminoglycoside inhibition of, ribosome recycling.
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Aminoglycosides are widely used antibiotics that cause messenger RNA decoding errors, block mRNA and transfer RNA translocation, and inhibit ribosome recycling. Ribosome recycling follows the termination of protein synthesis and is aided by ribosome recycling factor (RRF) in bacteria. The molecular mechanism by which aminoglycosides inhibit ribosome recycling is unknown. Here we show in X-ray crystal structures of the Escherichia coli 70S ribosome that RRF binding causes RNA helix H69 of the large ribosomal subunit, which is crucial for subunit association, to swing away from the subunit interface. Aminoglycosides bind to H69 and completely restore the contacts between ribosomal subunits that are disrupted by RRF. These results provide a structural explanation for aminoglycoside inhibition of ribosome recycling.
==About this Structure==
==About this Structure==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Thermus thermophilus]]
[[Category: Thermus thermophilus]]
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[[Category: Borovinskaya, M.A.]]
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[[Category: Borovinskaya, M A.]]
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[[Category: Cate, J.H.D.]]
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[[Category: Cate, J H.D.]]
[[Category: Hirokawa, G.]]
[[Category: Hirokawa, G.]]
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[[Category: Holton, J.M.]]
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[[Category: Holton, J M.]]
[[Category: Kaji, A.]]
[[Category: Kaji, A.]]
[[Category: Kaji, H.]]
[[Category: Kaji, H.]]
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[[Category: Pai, R.D.]]
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[[Category: Pai, R D.]]
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[[Category: Schuwirth, B.S.]]
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[[Category: Schuwirth, B S.]]
[[Category: Zhang, W.]]
[[Category: Zhang, W.]]
[[Category: LLL]]
[[Category: LLL]]
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[[Category: rna-protein complex]]
[[Category: rna-protein complex]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 13:29:37 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:37:52 2008''

Revision as of 16:37, 21 February 2008


2qbi, resolution 4.0Å

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Crystal structure of the bacterial ribosome from Escherichia coli in complex with gentamicin and ribosome recycling factor (RRF). This file contains the 50S subunit of the first 70S ribosome, with gentamicin and RRF bound. The entire crystal structure contains two 70S ribosomes and is described in remark 400.

Overview

Aminoglycosides are widely used antibiotics that cause messenger RNA decoding errors, block mRNA and transfer RNA translocation, and inhibit ribosome recycling. Ribosome recycling follows the termination of protein synthesis and is aided by ribosome recycling factor (RRF) in bacteria. The molecular mechanism by which aminoglycosides inhibit ribosome recycling is unknown. Here we show in X-ray crystal structures of the Escherichia coli 70S ribosome that RRF binding causes RNA helix H69 of the large ribosomal subunit, which is crucial for subunit association, to swing away from the subunit interface. Aminoglycosides bind to H69 and completely restore the contacts between ribosomal subunits that are disrupted by RRF. These results provide a structural explanation for aminoglycoside inhibition of ribosome recycling.

About this Structure

2QBI is a Protein complex structure of sequences from Escherichia coli and Thermus thermophilus with , and as ligands. Full crystallographic information is available from OCA.

Reference

Structural basis for aminoglycoside inhibition of bacterial ribosome recycling., Borovinskaya MA, Pai RD, Zhang W, Schuwirth BS, Holton JM, Hirokawa G, Kaji H, Kaji A, Cate JH, Nat Struct Mol Biol. 2007 Aug;14(8):727-32. Epub 2007 Jul 29. PMID:17660832

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