View source for 9qdr


==Structure of Staphylococcus aureus MarR-type repressor MhqR==
<StructureSection load='9qdr' size='340' side='right'caption='[[9qdr]], [[Resolution|resolution]] 1.55&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[9qdr]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Staphylococcus_aureus Staphylococcus aureus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9QDR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9QDR FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.55&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=PGE:TRIETHYLENE+GLYCOL'>PGE</scene></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9qdr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9qdr OCA], [https://pdbe.org/9qdr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9qdr RCSB], [https://www.ebi.ac.uk/pdbsum/9qdr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9qdr ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/W8U802_STAAU W8U802_STAAU] 
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
The MarR-family regulator MhqR of Staphylococcus aureus (SaMhqR) was previously characterized as a quinone-sensing repressor of the mhqRED operon. Here, we solved the crystal structures of apo-SaMhqR and the 2-methylbenzoquinone (MBQ)-bound SaMhqR complex. AlphaFold3 modeling was used to predict the structure of SaMhqR in complex with its operator DNA. In the DNA-bound SaMhqR state, S65 and S66 of an allosteric alpha3-alpha4 loop adopted a helically wound conformation to elongate helix alpha4 for optimal DNA binding. Key residues for MBQ interaction were identified as F11, F39, E43, and H111, forming the MBQ-binding pocket. MBQ binding prevented the formation of the extended helix alpha4 in the allosteric loop, leading to steric clashes with the DNA. Molecular dynamics (MD) simulations revealed an increased intrinsic dynamics within the allosteric loop and the beta1/beta2-wing regions after MBQ binding to prevent DNA binding. Using mutational analyses, we validated that F11, F39, and H111 are required for quinone sensing in vivo, whereas S65 and S66 of the allosteric loop and D88, K89, V91, and Y92 of the beta1/beta2-wing are essential for DNA binding in vitro and in vivo. In conclusion, our structure-guided modeling and mutational analyses identified a quinone-binding pocket in SaMhqR and the mechanism of SaMhqR inactivation, which involves local structural rearrangements of an allosteric loop and high intrinsic dynamics to prevent DNA interactions. Our results provide novel insights into the redox mechanism of the conserved SaMhqR repressor, which functions as an important determinant of quinone and antimicrobial resistance in S. aureus.IMPORTANCEStaphylococcus aureus is a major human pathogen that can cause life-threatening infections in humans. However, treatment options are limited due to the prevalence of antimicrobial-resistant isolates in the hospital and the community. The MarR-type repressor SaMhqR was described to control resistance toward quinones and quinone-like antimicrobials. However, the redox-regulatory mechanism of SaMhqR by quinones was unknown. In this work, we explored the DNA-binding and quinone-sensing mechanism of SaMhqR and identified a quinone-binding pocket and an allosteric loop, which facilitates DNA binding activity via a helical wound conformation and adapts an unstructured coiled conformation upon quinone binding to inhibit DNA binding. A similar mechanism has been recently discovered for the regulation of uric acid resistance by UrtR family repressors (W. S. Song, D. U. Ki , H. Y. Cho, O. H. Kwon, H. Cho, S. I. Yoon, Nucleic Acids Res 52:13192-13205, 2024, https://doi.org/10.1093/nar/gkae922). Our results contribute to a better understanding of antimicrobial resistance regulation, which may be exploited for future drug design to combat multidrug-resistant S. aureus.

Structural basis of quinone sensing by the MarR-type repressor MhqR in Staphylococcus aureus.,Nguyen TT-P, Weiland P, Loi VV, Kiontke S, Burchert F, Zegarra V, Kern A, Fritsch VN, Baranov D, Bronowska AK, Bange G, Antelmann H mBio. 2025 Dec 31:e0329225. doi: 10.1128/mbio.03292-25. PMID:41474324<ref>PMID:41474324</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 9qdr" style="background-color:#fffaf0;"></div>
== References ==
<references/>
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</StructureSection>
[[Category: Large Structures]]
[[Category: Staphylococcus aureus]]
[[Category: Bange G]]
[[Category: Kiontke S]]
[[Category: Weiland P]]