4m3g

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(New page: '''Unreleased structure''' The entry 4m3g is ON HOLD Authors: Villemagne, B., Flipo, M., Blondiaux, N., Crauste, C., Malaquin, S., Leroux, F., Piveteau, C., Villeret, V., Brodin, P., Vi...)
Current revision (12:23, 1 March 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 4m3g is ON HOLD
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==Rapid and efficient design of new inhibitors of Mycobacterium tuberculosis transcriptional repressor EthR using fragment growing, merging and linking approaches==
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<StructureSection load='4m3g' size='340' side='right'caption='[[4m3g]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4m3g]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Mycobacterium_tuberculosis_H37Rv Mycobacterium tuberculosis H37Rv]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4M3G OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4M3G FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.3&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=2G1:4-(2-METHYL-1,3-THIAZOL-4-YL)-N-(3,3,3-TRIFLUOROPROPYL)BENZENESULFONAMIDE'>2G1</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4m3g FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4m3g OCA], [https://pdbe.org/4m3g PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4m3g RCSB], [https://www.ebi.ac.uk/pdbsum/4m3g PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4m3g ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/ETHR_MYCTU ETHR_MYCTU] Involved in the repression of the monooxygenase EthA which is responsible of the formation of the active metabolite of ethionamide (ETH).<ref>PMID:10869356</ref> <ref>PMID:10944230</ref>
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Authors: Villemagne, B., Flipo, M., Blondiaux, N., Crauste, C., Malaquin, S., Leroux, F., Piveteau, C., Villeret, V., Brodin, P., Villoutreix, B., Sperandio, O., Wohlkonig, A., Wintjens, R., Deprez, B., Baulard, A., Willand, N.
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==See Also==
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*[[Tetracycline repressor protein 3D structures|Tetracycline repressor protein 3D structures]]
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Description: Rapid and efficient design of new inhibitors of Mycobacterium tuberculosis transcriptional repressor EthR using Fragment growing, merging and linking approaches.
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Mycobacterium tuberculosis H37Rv]]
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[[Category: Baulard A]]
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[[Category: Blondiaux N]]
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[[Category: Brodin P]]
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[[Category: Crauste C]]
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[[Category: Deprez B]]
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[[Category: Flipo M]]
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[[Category: Leroux F]]
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[[Category: Malaquin S]]
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[[Category: Piveteau C]]
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[[Category: Sperandio O]]
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[[Category: Villemagne B]]
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[[Category: Villeret V]]
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[[Category: Villoutreix B]]
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[[Category: Willand N]]
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[[Category: Wintjens R]]
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[[Category: Wohlkonig A]]

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Rapid and efficient design of new inhibitors of Mycobacterium tuberculosis transcriptional repressor EthR using fragment growing, merging and linking approaches

PDB ID 4m3g

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