5hs8

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==Crystal structure of the diamide-treated YodB from B. subtilis==
==Crystal structure of the diamide-treated YodB from B. subtilis==
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<StructureSection load='5hs8' size='340' side='right' caption='[[5hs8]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
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<StructureSection load='5hs8' size='340' side='right'caption='[[5hs8]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[5hs8]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5HS8 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5HS8 FirstGlance]. <br>
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<table><tr><td colspan='2'>[[5hs8]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Bacillus_subtilis_subsp._subtilis_str._168 Bacillus subtilis subsp. subtilis str. 168]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5HS8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5HS8 FirstGlance]. <br>
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</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5hs7|5hs7]], [[5hs9|5hs9]]</td></tr>
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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&#8491;</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=5hs8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5hs8 OCA], [http://pdbe.org/5hs8 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5hs8 RCSB], [http://www.ebi.ac.uk/pdbsum/5hs8 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5hs8 ProSAT]</span></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=5hs8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5hs8 OCA], [https://pdbe.org/5hs8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5hs8 RCSB], [https://www.ebi.ac.uk/pdbsum/5hs8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5hs8 ProSAT]</span></td></tr>
</table>
</table>
== Function ==
== Function ==
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[[http://www.uniprot.org/uniprot/YODB_BACSU YODB_BACSU]] Negatively regulates yodC and azoR1 which may contribute to the degradation of aromatic compounds. Probably positively regulates the catechol-specific transcription of mhqNOP, mhqED, and mhqA.<ref>PMID:18208493</ref>
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[https://www.uniprot.org/uniprot/YODB_BACSU YODB_BACSU] Negatively regulates yodC and azoR1 which may contribute to the degradation of aromatic compounds. Probably positively regulates the catechol-specific transcription of mhqNOP, mhqED, and mhqA.<ref>PMID:18208493</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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For bacteria, cysteine thiol groups in proteins are commonly used as thiol-based switches for redox sensing to activate specific detoxification pathways and restore the redox balance. Among the known thiol-based regulatory systems, the MarR/DUF24 family regulators have been reported to sense and respond to reactive electrophilic species, including diamide, quinones, and aldehydes, with high specificity. Here, we report that the prototypical regulator YodB of the MarR/DUF24 family from Bacillus subtilis uses two distinct pathways to regulate transcription in response to two reactive electrophilic species (diamide or methyl-p-benzoquinone), as revealed by X-ray crystallography, NMR spectroscopy, and biochemical experiments. Diamide induces structural changes in the YodB dimer by promoting the formation of disulfide bonds, whereas methyl-p-benzoquinone allows the YodB dimer to be dissociated from DNA, with little effect on the YodB dimer. The results indicate that B. subtilis may discriminate toxic quinones, such as methyl-p-benzoquinone, from diamide to efficiently manage multiple oxidative signals. These results also provide evidence that different thiol-reactive compounds induce dissimilar conformational changes in the regulator to trigger the separate regulation of target DNA. This specific control of YodB is dependent upon the type of thiol-reactive compound present, is linked to its direct transcriptional activity, and is important for the survival of B. subtilis This study of B. subtilis YodB also provides a structural basis for the relationship that exists between the ligand-induced conformational changes adopted by the protein and its functional switch.
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Two distinct mechanisms of transcriptional regulation by the redox sensor YodB.,Lee SJ, Lee IG, Lee KY, Kim DG, Eun HJ, Yoon HJ, Chae S, Song SH, Kang SO, Seo MD, Kim HS, Park SJ, Lee BJ Proc Natl Acad Sci U S A. 2016 Aug 30;113(35):E5202-11. doi:, 10.1073/pnas.1604427113. Epub 2016 Aug 16. PMID:27531959<ref>PMID:27531959</ref>
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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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<div class="pdbe-citations 5hs8" style="background-color:#fffaf0;"></div>
== References ==
== References ==
<references/>
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Lee, B J]]
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[[Category: Bacillus subtilis subsp. subtilis str. 168]]
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[[Category: Lee, I G]]
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[[Category: Large Structures]]
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[[Category: Lee, S J]]
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[[Category: Lee BJ]]
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[[Category: Dna binding protein]]
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[[Category: Lee IG]]
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[[Category: Hth-type transcriptional regulator]]
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[[Category: Lee SJ]]
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[[Category: Oxidized form]]
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Current revision

Crystal structure of the diamide-treated YodB from B. subtilis

PDB ID 5hs8

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