1fyp

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|PDB= 1fyp |SIZE=350|CAPTION= <scene name='initialview01'>1fyp</scene>
|PDB= 1fyp |SIZE=350|CAPTION= <scene name='initialview01'>1fyp</scene>
|SITE=
|SITE=
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|LIGAND= <scene name='pdbligand=PAR:PAROMOMYCIN'>PAR</scene>
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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=PAR:PAROMOMYCIN'>PAR</scene>, <scene name='pdbligand=U:URIDINE-5&#39;-MONOPHOSPHATE'>U</scene>
|ACTIVITY=
|ACTIVITY=
|GENE=
|GENE=
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|DOMAIN=
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|RELATEDENTRY=[[1fyo|1FYO]], [[1pbr|1PBR]], [[1a3m|1A3M]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1fyp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1fyp OCA], [http://www.ebi.ac.uk/pdbsum/1fyp PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1fyp RCSB]</span>
}}
}}
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[[Category: Lynch, S R.]]
[[Category: Lynch, S R.]]
[[Category: Puglisi, J D.]]
[[Category: Puglisi, J D.]]
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[[Category: PAR]]
 
[[Category: aminoglycoside]]
[[Category: aminoglycoside]]
[[Category: g-a base pair]]
[[Category: g-a base pair]]
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[[Category: stem-internal loop-stem-tetraloop]]
[[Category: stem-internal loop-stem-tetraloop]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 11:15:48 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 20:32:52 2008''

Revision as of 17:32, 30 March 2008


PDB ID 1fyp

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Ligands: , , , ,
Related: 1FYO, 1PBR, 1A3M


Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



EUKARYOTIC DECODING REGION A-SITE RNA-PAROMOMYCIN COMPLEX


Overview

Aminoglycoside antibiotics, including paromomycin, neomycin and gentamicin, target a region of highly conserved nucleotides in the decoding region aminoacyl-tRNA site (A site) of 16 S rRNA on the 30 S subunit. Change of a single nucleotide, A1408 to G, reduces the affinity of many aminoglycosides for the ribosome; G1408 distinguishes between prokaryotic and eukaryotic ribosomes. The structures of a prokaryotic decoding region A-site oligonucleotide free in solution and bound to the aminoglycosides paromomycin and gentamicin C1a were determined previously. Here, the structure of a eukaryotic decoding region A-site oligonucleotide bound to paromomycin has been determined using NMR spectroscopy and compared to the prokaryotic A-site-paromomycin structure. A conformational change in three adenosine residues of an internal loop, critical for high-affinity antibiotic binding, was observed in the prokaryotic RNA-paromomycin complex in comparison to its free form. This conformational change is not observed in the eukaryotic RNA-paromomycin complex, disrupting the binding pocket for ring I of the antibiotic. The lack of the conformational change supports footprinting and titration calorimetry data that demonstrate approximately 25-50-fold weaker binding of paromomycin to the eukaryotic decoding-site oligonucleotide. Neomycin, which is much less active against Escherichia coli ribosomes with an A1408G mutation, binds non-specifically to the oligonucleotide. These results suggest that eukaryotic ribosomal RNA has a shallow binding pocket for aminoglycosides, which accommodates only certain antibiotics.

About this Structure

1FYP is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

Structural origins of aminoglycoside specificity for prokaryotic ribosomes., Lynch SR, Puglisi JD, J Mol Biol. 2001 Mar 9;306(5):1037-58. PMID:11237617

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