1byl

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(New page: 200px<br /><applet load="1byl" size="450" color="white" frame="true" align="right" spinBox="true" caption="1byl, resolution 2.3&Aring;" /> '''BLEOMYCIN RESISTANCE ...)
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'''BLEOMYCIN RESISTANCE PROTEIN FROM STREPTOALLOTEICHUS HINDUSTANUS'''<br />
'''BLEOMYCIN RESISTANCE PROTEIN FROM STREPTOALLOTEICHUS HINDUSTANUS'''<br />
==Overview==
==Overview==
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The antibiotic bleomycin, a strong DNA cutting agent, is naturally, produced by actinomycetes which have developed a resistance mechanism, against such a lethal compound. The crystal structure, at 2.3 A, resolution, of a bleomycin resistance protein of 14 kDa reveals a, structure in two halves with the same alpha/beta fold despite no sequence, similarity. The crystal packing shows compact dimers with a hydrophobic, interface and involved in mutual chain exchange. Two independent solution, studies (analytical centrifugation and light scattering) showed that this, dimeric form is not a packing artefact but is indeed the functional one., Furthermore, light scattering also showed that one dimer binds two, antibiotic molecules as expected. A crevice located at the dimer, interface, as well as the results of a site-directed mutagenesis study, led to a model wherein two bleomycin molecules are completely sequestered, by one dimer. This provides a novel insight into antibiotic resistance due, to drug sequestering, and probably also into drug transport and excretion.
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The antibiotic bleomycin, a strong DNA cutting agent, is naturally produced by actinomycetes which have developed a resistance mechanism against such a lethal compound. The crystal structure, at 2.3 A resolution, of a bleomycin resistance protein of 14 kDa reveals a structure in two halves with the same alpha/beta fold despite no sequence similarity. The crystal packing shows compact dimers with a hydrophobic interface and involved in mutual chain exchange. Two independent solution studies (analytical centrifugation and light scattering) showed that this dimeric form is not a packing artefact but is indeed the functional one. Furthermore, light scattering also showed that one dimer binds two antibiotic molecules as expected. A crevice located at the dimer interface, as well as the results of a site-directed mutagenesis study, led to a model wherein two bleomycin molecules are completely sequestered by one dimer. This provides a novel insight into antibiotic resistance due to drug sequestering, and probably also into drug transport and excretion.
==About this Structure==
==About this Structure==
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1BYL is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Streptoalloteichus_hindustanus Streptoalloteichus hindustanus]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1BYL OCA].
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1BYL is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Streptoalloteichus_hindustanus Streptoalloteichus hindustanus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1BYL OCA].
==Reference==
==Reference==
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[[Category: Cagnon, C.]]
[[Category: Cagnon, C.]]
[[Category: Dumas, P.]]
[[Category: Dumas, P.]]
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[[Category: Masson, J.M.]]
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[[Category: Masson, J M.]]
[[Category: antibiotic resistance]]
[[Category: antibiotic resistance]]
[[Category: bleomycin]]
[[Category: bleomycin]]
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[[Category: drug sequestering]]
[[Category: drug sequestering]]
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Revision as of 10:00, 21 February 2008


1byl, resolution 2.3Å

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BLEOMYCIN RESISTANCE PROTEIN FROM STREPTOALLOTEICHUS HINDUSTANUS

Overview

The antibiotic bleomycin, a strong DNA cutting agent, is naturally produced by actinomycetes which have developed a resistance mechanism against such a lethal compound. The crystal structure, at 2.3 A resolution, of a bleomycin resistance protein of 14 kDa reveals a structure in two halves with the same alpha/beta fold despite no sequence similarity. The crystal packing shows compact dimers with a hydrophobic interface and involved in mutual chain exchange. Two independent solution studies (analytical centrifugation and light scattering) showed that this dimeric form is not a packing artefact but is indeed the functional one. Furthermore, light scattering also showed that one dimer binds two antibiotic molecules as expected. A crevice located at the dimer interface, as well as the results of a site-directed mutagenesis study, led to a model wherein two bleomycin molecules are completely sequestered by one dimer. This provides a novel insight into antibiotic resistance due to drug sequestering, and probably also into drug transport and excretion.

About this Structure

1BYL is a Single protein structure of sequence from Streptoalloteichus hindustanus. Full crystallographic information is available from OCA.

Reference

Crystal structure and site-directed mutagenesis of a bleomycin resistance protein and their significance for drug sequestering., Dumas P, Bergdoll M, Cagnon C, Masson JM, EMBO J. 1994 Jun 1;13(11):2483-92. PMID:7516875

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