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2pwt

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(New page: 200px<br /><applet load="2pwt" size="350" color="white" frame="true" align="right" spinBox="true" caption="2pwt, resolution 1.800&Aring;" /> '''Crystal structure o...)
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==Overview==
==Overview==
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The crystal structure of the complex between oligonucleotide containing, the bacterial ribosomal decoding site (A site) and the synthetic, paromomycin analogue 1, which contains the, gamma-amino-alpha-hydroxybutyryl (L-haba) group at position N1 of ring II, (2-DOS ring), and an ether chain with an O-phenethylaminoethyl group at, position C2'' of ring III, is reported. Interestingly, next to the, paromomycin analogue 1 specifically bound to the A site, a second molecule, of 1 with a different conformation is observed at the crystal packing, interface which mimics the A-minor interaction between two bulged-out, adenines from the A site and the codon-anticodon stem of the mRNA-tRNA, complex. Improved antibacterial activity supports the conclusion that, analogue 1 might affect protein synthesis on the ribosome in two different, ways: 1) specific binding to the A site forces maintenance of the "on", state with two bulged out adenines, and 2) a new binding mode of 1 to an, A-minor motif which stabilizes complex formation between the ribosome and, the mRNA-tRNA complex regardless of whether the codon-anticodon stem is of, the cognate or near-cognate type.
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The crystal structure of the complex between oligonucleotide containing the bacterial ribosomal decoding site (A site) and the synthetic paromomycin analogue 1, which contains the gamma-amino-alpha-hydroxybutyryl (L-haba) group at position N1 of ring II (2-DOS ring), and an ether chain with an O-phenethylaminoethyl group at position C2'' of ring III, is reported. Interestingly, next to the paromomycin analogue 1 specifically bound to the A site, a second molecule of 1 with a different conformation is observed at the crystal packing interface which mimics the A-minor interaction between two bulged-out adenines from the A site and the codon-anticodon stem of the mRNA-tRNA complex. Improved antibacterial activity supports the conclusion that analogue 1 might affect protein synthesis on the ribosome in two different ways: 1) specific binding to the A site forces maintenance of the "on" state with two bulged out adenines, and 2) a new binding mode of 1 to an A-minor motif which stabilizes complex formation between the ribosome and the mRNA-tRNA complex regardless of whether the codon-anticodon stem is of the cognate or near-cognate type.
==About this Structure==
==About this Structure==
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==Reference==
==Reference==
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Crystal Structure of the Bacterial Ribosomal Decoding Site Complexed with a Synthetic Doubly Functionalized Paromomycin Derivative: a New Specific Binding Mode to an A-Minor Motif Enhances in vitro Antibacterial Activity., Kondo J, Pachamuthu K, Francois B, Szychowski J, Hanessian S, Westhof E, ChemMedChem. 2007 Aug 27;. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=17722211 17722211]
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Crystal Structure of the Bacterial Ribosomal Decoding Site Complexed with a Synthetic Doubly Functionalized Paromomycin Derivative: a New Specific Binding Mode to an A-Minor Motif Enhances in vitro Antibacterial Activity., Kondo J, Pachamuthu K, Francois B, Szychowski J, Hanessian S, Westhof E, ChemMedChem. 2007 Nov 12;2(11):1631-1638. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=17722211 17722211]
[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Francois, B.]]
[[Category: Francois, B.]]
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[[Category: aminoglycoside; haba group; ribosomal decoding site; x-ray analysis; rna]]
[[Category: aminoglycoside; haba group; ribosomal decoding site; x-ray analysis; rna]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 12:05:08 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:33:46 2008''

Revision as of 16:33, 21 February 2008


2pwt, resolution 1.800Å

Drag the structure with the mouse to rotate

Crystal structure of the bacterial ribosomal decoding site complexed with aminoglycoside containing the L-HABA group

Overview

The crystal structure of the complex between oligonucleotide containing the bacterial ribosomal decoding site (A site) and the synthetic paromomycin analogue 1, which contains the gamma-amino-alpha-hydroxybutyryl (L-haba) group at position N1 of ring II (2-DOS ring), and an ether chain with an O-phenethylaminoethyl group at position C2 of ring III, is reported. Interestingly, next to the paromomycin analogue 1 specifically bound to the A site, a second molecule of 1 with a different conformation is observed at the crystal packing interface which mimics the A-minor interaction between two bulged-out adenines from the A site and the codon-anticodon stem of the mRNA-tRNA complex. Improved antibacterial activity supports the conclusion that analogue 1 might affect protein synthesis on the ribosome in two different ways: 1) specific binding to the A site forces maintenance of the "on" state with two bulged out adenines, and 2) a new binding mode of 1 to an A-minor motif which stabilizes complex formation between the ribosome and the mRNA-tRNA complex regardless of whether the codon-anticodon stem is of the cognate or near-cognate type.

About this Structure

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

Reference

Crystal Structure of the Bacterial Ribosomal Decoding Site Complexed with a Synthetic Doubly Functionalized Paromomycin Derivative: a New Specific Binding Mode to an A-Minor Motif Enhances in vitro Antibacterial Activity., Kondo J, Pachamuthu K, Francois B, Szychowski J, Hanessian S, Westhof E, ChemMedChem. 2007 Nov 12;2(11):1631-1638. PMID:17722211

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