1jzz

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[[Image:1jzz.gif|left|200px]]
[[Image:1jzz.gif|left|200px]]
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{{Structure
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<!--
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|PDB= 1jzz |SIZE=350|CAPTION= <scene name='initialview01'>1jzz</scene>, resolution 3.8&Aring;
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The line below this paragraph, containing "STRUCTURE_1jzz", creates the "Structure Box" on the page.
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|SITE=
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|LIGAND= <scene name='pdbligand=A:ADENOSINE-5&#39;-MONOPHOSPHATE'>A</scene>, <scene name='pdbligand=C:CYTIDINE-5&#39;-MONOPHOSPHATE'>C</scene>, <scene name='pdbligand=G:GUANOSINE-5&#39;-MONOPHOSPHATE'>G</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=ROX:ROXITHROMYCIN'>ROX</scene>, <scene name='pdbligand=U:URIDINE-5&#39;-MONOPHOSPHATE'>U</scene>, <scene name='pdbligand=Y:2&#39;-DEOXY-N6-(S)STYRENE+OXIDE+ADENOSINE+MONOPHOSPHATE'>Y</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY=
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|GENE=
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|DOMAIN=
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{{STRUCTURE_1jzz| PDB=1jzz | SCENE= }}
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|RELATEDENTRY=[[1jzx|1JZX]], [[1jzy|1JZY]], [[1k00|1K00]], [[1k01|1K01]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1jzz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1jzz OCA], [http://www.ebi.ac.uk/pdbsum/1jzz PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1jzz RCSB]</span>
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}}
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'''Structural Basis for the Interaction of Antibiotics with the Peptidyl Transferase Center in Eubacteria'''
'''Structural Basis for the Interaction of Antibiotics with the Peptidyl Transferase Center in Eubacteria'''
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[[Category: 50]]
[[Category: 50]]
[[Category: 5]]
[[Category: 5]]
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[[Category: antibiotic]]
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[[Category: Antibiotic]]
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[[Category: peptidyl transferase center]]
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[[Category: Peptidyl transferase center]]
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[[Category: ribosome]]
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[[Category: Ribosome]]
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[[Category: roxithromycin]]
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[[Category: Roxithromycin]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 22:07:48 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 21:41:23 2008''
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Revision as of 19:07, 2 May 2008

Template:STRUCTURE 1jzz

Structural Basis for the Interaction of Antibiotics with the Peptidyl Transferase Center in Eubacteria


Overview

Ribosomes, the site of protein synthesis, are a major target for natural and synthetic antibiotics. Detailed knowledge of antibiotic binding sites is central to understanding the mechanisms of drug action. Conversely, drugs are excellent tools for studying the ribosome function. To elucidate the structural basis of ribosome-antibiotic interactions, we determined the high-resolution X-ray structures of the 50S ribosomal subunit of the eubacterium Deinococcus radiodurans, complexed with the clinically relevant antibiotics chloramphenicol, clindamycin and the three macrolides erythromycin, clarithromycin and roxithromycin. We found that antibiotic binding sites are composed exclusively of segments of 23S ribosomal RNA at the peptidyl transferase cavity and do not involve any interaction of the drugs with ribosomal proteins. Here we report the details of antibiotic interactions with the components of their binding sites. Our results also show the importance of putative Mg+2 ions for the binding of some drugs. This structural analysis should facilitate rational drug design.

About this Structure

1JZZ is a Protein complex structure of sequences from Deinococcus radiodurans. Full crystallographic information is available from OCA.

Reference

Structural basis for the interaction of antibiotics with the peptidyl transferase centre in eubacteria., Schlunzen F, Zarivach R, Harms J, Bashan A, Tocilj A, Albrecht R, Yonath A, Franceschi F, Nature. 2001 Oct 25;413(6858):814-21. PMID:11677599 Page seeded by OCA on Fri May 2 22:07:48 2008

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