5f1j

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'''Unreleased structure'''
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==Structure of Transcriptional Regulatory Repressor Protein - EthR from Mycobacterium Tuberculosis in complex with compound 1 at 1.63A resolution==
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<StructureSection load='5f1j' size='340' side='right' caption='[[5f1j]], [[Resolution|resolution]] 1.63&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5f1j]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5F1J OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5F1J FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=5TO:3-CYCLOPENTYL-1-PYRROLIDIN-1-YL-PROPAN-1-ONE'>5TO</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5f1j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5f1j OCA], [http://pdbe.org/5f1j PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5f1j RCSB], [http://www.ebi.ac.uk/pdbsum/5f1j PDBsum]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/ETHR_MYCTO ETHR_MYCTO]] Involved in the repression of the monooxygenase EthA which is responsible of the formation of the active metabolite of ethionamide (ETH).
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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With the ever-increasing instances of resistance to frontline TB drugs there is the need to develop novel strategies to fight the worldwide TB epidemic. Boosting the effect of the existing second-line antibiotic ethionamide by inhibiting the mycobacterial transcriptional repressor protein EthR is an attractive therapeutic strategy. Herein we report the use of a fragment based drug discovery approach for the structure-guided systematic merging of two fragment molecules, each binding twice to the hydrophobic cavity of EthR from M. tuberculosis. These together fill the entire binding pocket of EthR. We elaborated these fragment hits and developed small molecule inhibitors which have a 100-fold improvement of potency in vitro over the initial fragments.
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The entry 5f1j is ON HOLD until Paper Publication
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A fragment merging approach towards the development of small molecule inhibitors of Mycobacterium tuberculosis EthR for use as ethionamide boosters.,Nikiforov PO, Surade S, Blaszczyk M, Delorme V, Brodin P, Baulard AR, Blundell TL, Abell C Org Biomol Chem. 2016 Jan 25. PMID:26806381<ref>PMID:26806381</ref>
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Authors: Surade, S., Blaszczyk, M., Nikiforov, P.O., Abell, C., Blundell, T.L.
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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Description: Structure of Transcriptional Regulatory Repressor Protein -EthR from Mycobacterium Tuberculosis in complex with compound 1 at 1.63A resolution
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<div class="pdbe-citations 5f1j" style="background-color:#fffaf0;"></div>
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[[Category: Unreleased Structures]]
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== References ==
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<references/>
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__TOC__
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</StructureSection>
[[Category: Abell, C]]
[[Category: Abell, C]]
[[Category: Blaszczyk, M]]
[[Category: Blaszczyk, M]]
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[[Category: Nikiforov, P.O]]
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[[Category: Blundell, T L]]
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[[Category: Blundell, T.L]]
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[[Category: Nikiforov, P O]]
[[Category: Surade, S]]
[[Category: Surade, S]]
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[[Category: Ethr]]
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[[Category: Mycobacterium tuberculosis]]
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[[Category: Repressor]]
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[[Category: Transcription]]

Revision as of 15:39, 3 February 2016

Structure of Transcriptional Regulatory Repressor Protein - EthR from Mycobacterium Tuberculosis in complex with compound 1 at 1.63A resolution

5f1j, resolution 1.63Å

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