MarR family transcription factors.

Ligand-responsive Transcriptional Regulation by Members of the MarR Family of Winged Helix Proteins

Wilkinson, S. P., & Grove, A. (2006) · Current Issues in Molecular Biology · doi:10.21775/cimb.008.051 · Cited by 269

Regulation of virulence by members of the MarR/SlyA family

Ellison, D. W., & Miller, V. L. (2006) · Current Opinion in Microbiology · doi:10.1016/j.mib.2006.02.003 · Cited by 203

Molecular Mechanisms of Ligand-Mediated Attenuation of DNA Binding by MarR Family Transcriptional Regulators

Perera, I. C., & Grove, A. (2010) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjq021 · Cited by 195

Structural study of TcaR and its complexes with multiple antibiotics from Staphylococcus epidermidis

Chang, Y.-M., Jeng, W. Y., Ko, T., Yeh, Y.-J., Chen, C. K.-M., & Wang, A. H. ‐. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913302107 · Cited by 87

Structural Insight into the Mechanism of DNA-Binding Attenuation of the Neisserial Adhesin Repressor NadR by the Small Natural Ligand 4-Hydroxyphenylacetic Acid

Brier, S., Fagnocchi, L., Donnarumma, D., Scarselli, M., Rappuoli, R., Nissum, M., Delany, I., & Norais, N. (2012) · Biochemistry · doi:10.1021/bi300656w · Cited by 24

One-Component Systems that Regulate the Expression of Degradation Pathways for Aromatic Compounds

Durante‐Rodríguez, G., Gómez‐Álvarez, H., Nogales, J., Carmona, M., & Dı́az, E. (2016) · Springer eBooks · doi:10.1007/978-3-319-20796-4_5-1 · Cited by 6

Characterization of transcriptional regulator PicR of picolinic acid-degrading bacterium Bordetella petrii strain MY10

Wang, X., Xu, L., Xu, Q., Wang, K., Xu, L., Jiang, Y., Xu, S., Hong, Q., He, J., & Qiu, J. (2023) · International Biodeterioration & Biodegradation · doi:10.1016/j.ibiod.2023.105646 · Cited by 5

The Ku–Mar zinc finger: A segment-swapped zinc ribbon in MarR-like transcription regulators related to the Ku bridge

Kaur, G., & Subramanian, S. (2015) · Journal of Structural Biology · doi:10.1016/j.jsb.2015.07.011 · Cited by 5

Structure of the MarR family protein Rv0880 fromMycobacterium tuberculosis

Gao, Y.-R., Feng, N., Chen, T., Li, D.-F., & Bi, L.-J. (2015) · Acta Crystallographica Section F Structural Biology Communications · doi:10.1107/s2053230x15007281 · Cited by 5

Functional analysis of Bucella reveals transcriptional regulation of MarR

Deng, X., Li, M., Liu, L., Zhang, J., Zhang, Y., Guo, J., Zhao, T., Cao, S., Li, Z., & Zhang, H. (2020) · Microbial Pathogenesis · doi:10.1016/j.micpath.2020.104201 · Cited by 5

Exploring the eco-evolutionary role of plasmids and defense systems in ‘Fervidacidithiobacillus caldus’ extreme acidophile

Pacheco-Acosta, S., Castro-Toro, G., Rojas-Villalobos, C., Valenzuela, C., Haristoy, J. J., Zapata-Araya, A., Moya-Beltrán, A., Sepúlveda-Rebolledo, P., Pérez‐Rueda, E., Ulloa, R. J., et al. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1610279 · Cited by 4

Host-driven evolution shapes the polysaccharide utilization profiles of alga-associated Flavobacteriaceae

Cai, G., Wu, Y., Chen, Z., Yang, X., Jiang, X., Wang, Q., Cai, R., & Wang, H. (2026) · Microbiome · doi:10.1186/s40168-025-02321-5 · Cited by 5

MarR family regulator LcbR2 activates lincomycin biosynthesis in multiple ways

Wang, R., Chen, L., Zhao, J., Gao, Y., Zhou, T., Jiang, Y., Wu, H., & Zhang, H. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.140292 · Cited by 4

Small-angle x-ray and neutron scattering of MexR and its complex with DNA supports a conformational selection binding model

Caporaletti, F., Pietras, Z., Morad, V., Mårtensson, L., Gabel, F., Wallner, B., Martel, A., & Sunnerhagen, M. (2022) · Biophysical Journal · doi:10.1016/j.bpj.2022.11.2949 · Cited by 4

Study on the estradiol degradation gene expression and resistance mechanism of Rhodococcus R-001 under low-temperature stress

Qiu, Q., Li, H., Sun, X., Zhang, L., Tian, K., Chang, M., Li, S., Zhou, D., & Huo, H. (2024) · Chemosphere · doi:10.1016/j.chemosphere.2024.142146 · Cited by 4

A moonlighting function of Mycobacterium smegmatis Ku in zinc homeostasis?

Kushwaha, A. K., Deochand, D. K., & Grove, A. (2014) · Protein Science · doi:10.1002/pro.2612 · Cited by 4

BosR: A novel biofilm-specific regulator in Pseudomonas aeruginosa

Dostert, M., Belanger, C. R., Pedraz, L., Alford, M. A., Blimkie, T. M., Falsafi, R., Bains, M., Dhillon, B. K., Haney, C. H., Lee, A. H., et al. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1021021 · Cited by 3

Proteomics, Metabolomics and Docking Analyses Provide Insights into Adaptation Strategies of Staphylococcus warneri CPD1 to Osmotic Stress and Its Influence on Wheat Growth

Rathore, P., Arora, S., Karunakaran, A., Singh, P., Fathima, Y., Saraboji, K., Kumar, R., & Ramakrishna, W. (2024) · Molecular Biotechnology · doi:10.1007/s12033-024-01346-9 · Cited by 3

Comparative and Functional Analyses Reveal Conserved and Variable Regulatory Systems That Control Lasalocid Biosynthesis in Different Streptomyces Species

Liu, M., Wang, K., Wei, J., Liu, N., Niu, G., Tan, H., & Huang, Y. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.03852-22 · Cited by 3

Comparative Genome Analysis of Two Streptococcus suis Serotype 8 Strains Identifies Two New Virulence-Associated Genes

Sheng, Q., Xu, Q., Lan, Z., & Wu, Z. (2024) · Animals · doi:10.3390/ani14040572 · Cited by 3

The protocatechuic acid catabolism regulator PcaV inhibits lincomycin biosynthesis either directly or indirectly through the control of the expression of other regulatory or metabolic genes

Zhou, T., Wang, R., Jiang, W., Zhao, J., Jiang, Y., Wu, H., & Zhang, H. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.143649 · Cited by 3

SarZ inhibits the hemolytic activity through regulation of phenol soluble modulins in Staphylococcus epidermidis

Chen, X., Sun, H., Wang, W., Wang, H., Tan, R., & Zhu, T. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1476287 · Cited by 2

Transcriptional regulation of two redundant 3-bromo-4-hydroxybenzoate catabolic operons via two different regulatory modes in Pigmentiphaga kullae strain H8

Ke, Z., Yang, K., Zhang, Z., Guo, R., Gao, Y., Lan, M., Jiang, J., & Chen, K. (2025) · Applied and Environmental Microbiology · doi:10.1128/aem.02403-24 · Cited by 2

Integrated multiomics reveals starvation-driven keratin degradation and persistence in Fervidobacterium islandicum AW-1

Sung, J., Kim, J.-Y., Jin, H., Baek, J., Kim, N. E., Song, H. H., Bong, S., Lee, Y.-J., Kim, B.-C., Lee, D. Y., et al. (2026) · iScience · doi:10.1016/j.isci.2026.115755 · Cited by 2

Mechanistic insights into allosteric regulation of the reductase component of p -hydroxyphenylacetate 3-hydroxylase by p -hydroxyphenylacetate: a model for effector-controlled activity of redox enzymes

Visitsatthawong, S., Anuwan, P., Lawan, N., Chaiyen, P., & Wongnate, T. (2024) · RSC Chemical Biology · doi:10.1039/d4cb00213j · Cited by 2

Annotation of a hypothetical protein (WP_002969292.1) from Brucella abortus

Rauthan, K., Goel, D., & Kumar, S. (2019) · Bioinformation · doi:10.6026/97320630015315 · Cited by 2

A putative transcription regulator involved in the virulence attenuation of an acriflavine-resistant vaccine strain of Erysipelothrix rhusiopathiae, the causative agent of swine erysipelas

Shimoji, Y., Tsukio, M., Ogawa, Y., Shiraiwa, K., Nishikawa, S., & Eguchi, M. (2019) · Veterinary Microbiology · doi:10.1016/j.vetmic.2019.108488 · Cited by 2

Revelation of AbfR in regulation of mismatch repair and energy metabolism in S. epidermidis by integrated proteomic and metabolomic analysis

Gu, L., Liu, X., Wang, Y., Zhou, Y., Zhu, H., Huang, J. Y., Lan, L., Zheng, J., Yang, C., & Zhou, H. (2020) · Journal of Proteomics · doi:10.1016/j.jprot.2020.103900 · Cited by 2

Food pathogens

Liu, J., Luo, Y., Xu, Z., & Kjellerup, B. V. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819493-5.00011-x · Cited by 2

A novel antioxidant system in Lactococcus lactis N8

Yang, H., Xu, X., Liu, F., Wang, D., Xin, Y., & Qiao, M. (2026) · Food Bioscience · doi:10.1016/j.fbio.2026.108358 · Cited by 1

OseR, a bacterial redox sensor, regulates ergothioneine uptake via a Cys thiol switch, enhancing oxidative stress resistance and virulence

Zhu, X., Wu, Y., Yao, H., & Wu, Z. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103790 · Cited by 1

Adaptation without Dominance in Pseudomonas syringae Pathovars

Satterwhite, R. S., & Bergelson, J. M. (2025) · Microbial Ecology · doi:10.1007/s00248-025-02675-1 · Cited by 1

Repression via DNA looping by the Gram-positive global transcriptional regulator ScoC from Geobacillus

Shulami, S., Hadad, N., Ghrayeb, M., Pomyalov, S., Pazy, Y., Chai, L., Shoham, Y., & Shoham, G. (2025) · Communications Biology · doi:10.1038/s42003-025-08555-1 · Cited by 1

Biophysical and Biochemical Characterization of the Binding of the MarR-like Transcriptional Regulator Saro_0803 to the nov1 Promotor and Its Inhibition by Resveratrol

He, Z., Ke, Z., Wang, W., Liu, Y., Zhang, H., & Li, Y. (2023) · Biomolecules · doi:10.3390/biom13030541 · Cited by 1

The Role of Burkholderia thailandensis-Encoded MarR Homologs in Response to Host-Derived Signals

Gupta, A. (2016) · Louisiana State University · doi:10.31390/gradschool_dissertations.4449 · Cited by 1

From Regulation of Secondary Metabolites to Increased Virulence under Sublethal Dosage of Antibiotics: An Unprecedented Role of Global Regulator, MftR, in Burkholderia thailandensis

Thapa, S. S. (2020) · Louisiana State University · doi:10.31390/gradschool_dissertations.5382 · Cited by 1

The Genomic Landscape of Head and Neck Cancer-associated StreptococciPreprint

Mai, L., Bouras, G. S., Yeo, K. K. L., Hodge, J.-C., Barry, E. F., Krishnan, S., Wormald, P., Valentine, R. J., Psaltis, A. J., Vreugde, S., et al. (2026) · Research Square · doi:10.21203/rs.3.rs-8400357/v1 · Cited by 1

Human-targeted drugs extensively reshape regulatory networks controlling virulence and antibiotic resistance in Salmonella TyphimuriumPreprint

Amstalden, M. K., Olayo-Alarcón, R., Brenzinger, S., Debande, L., Zannoni, A., Fiore, E., Boudrioua, A., Rashidian, A., Kronenberger, T., Wagner, S., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.09.30.755304 · Cited by 1

Structural insights into protein-protein interactions governing regulation in transcription initiation and ubiquitination

Anandapadamanaban, M. (2015) · Linköping University Electronic Press eBooks · doi:10.3384/diss.diva-122468

MarR Family Transcriptional Regulators from Streptomyces coelicolor

Huang, H. (2013) · doi:10.31390/gradschool_dissertations.64

Breaking Conventions: OhrR, A Transcriptional Regulator from Burkholderia thailandensis

Pande, A. (2018) · Louisiana State University · doi:10.31390/gradschool_dissertations.4537

Fatores de transcrição da família MarR e resistência a antibióticos em Chromobacterium violaceum

Barroso, K. C. M. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.17.2018.tde-18042018-111802

Profiling proteomic responses of Staphylococcus aureus exposed to colostrum hexasaccharide (CHS) through label-free mass spectrometric profiling

Khazaal, S. S., & Abid, S. A. (2020) · AIP conference proceedings · doi:10.1063/5.0000391

Faculty Opinions recommendation of Comparative Transcriptomics of Cold Growth and Adaptive Features of a Eury- and Steno-Psychrophile.

Coker, J. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733821484.793567038

MYC and MexR interactions with DNA : a Small Angle Scattering perspective

Caporaletti, F. (2022) · Linköping studies in science and technology. Dissertations · doi:10.3384/9789179296087

1H, 13C, and 15N resonance assignments of SarA monomer from Staphylococcus aureus in complex with DNA

Fu, D., Duan, B., Dong, X., & Xia, B. (2023) · Biomolecular NMR Assignments · doi:10.1007/s12104-023-10140-8

The role and regulation of pulcherrimin during Bacillus subtilis biofilm development

Angelini, L. L. (2023) · doi:10.17760/d20531814

AtuR and MarR transcriptional repressors that sense fatty or naphthenic acids and regulate degradation or antimicrobial resistance operons in Pseudomonas sp. OST1909Preprint

Bookout, T., Dominquez, J., Wallace, S., Goff, K. L., Shideler, S., Gieg, L. M., & Lewenza, S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.24.678253

Effects of 17β-Estradiol and Testosterone on Nocardia brasiliensis Gene Expression

Hernández, F. H., Paredes-Amaya, C. C., Jasso-Escutia, L. V., Córdova-Martínez, E., & Manzano–Gayosso, P. (2025) · Advances in Microbiology · doi:10.4236/aim.2025.1510038

Additional file 2 of Human reference gut microbiome catalog including newly assembled genomes from under-represented Asian metagenomes

Kim, C. Y., Lee, M., Yang, S., Kim, K., Yong, D., Kim, H. R., & Lee, I. (2021) · Figshare · doi:10.6084/m9.figshare.16456608

In silico analysis of pathogenic islands and metabolic pathways for understanding infection biology and lifestyle of Clostridium chauvoei

Pasam, K., Challa, S., & Neelapu, N. R. R. (2026) · Journal of Applied Biology & Biotechnology · doi:10.7324/jabb.2026.253744

Structural insights into HpaR-mediated recognition of hrpX and hrpG in Xanthomonas campestris pv. campestris

Zuo, M., Guo, Q., Ning, X., Wei, J., Huang, X., Zhang, D., Su, Z., Ming, Z., & Fu, Q. (2026) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2026.153429

Development of a functional screen for MreB mutants in Bacillus subtilis and characterization of a putative MreB effector

Campillo, A. D. S. E. (2017) · theses.fr (ABES) · doi:10.70675/665f400dze2cbz4736zb9d1z3083b100ddd5

Mitigating protocatechuic acid toxicity in Vibrio natriegens enables poly-3-hydroxybutyrate production from an aromatic carbon source

Faber, A., Politan, R. J., Nicol, A., Valle, S. D., Jenkins, B., Flematti, G. R., & Fritz, G. (2026) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-026-13831-z

The MarR family regulator RmaH underlies the trade-off between acid sensitivity and antibiotic tolerance in Lactococcus lactis

Song, Q., Zhang, P., Wu, H., Zhu, H., Jia-heng, L., & Qiao, J. (2026) · Journal of Bacteriology · doi:10.1128/jb.00502-25

The AcasR-FadD9 regulatory axis modulates iron homeostasis and susceptibility to the anti-mycobacterial compound ACA

Huang, F., Wang, Z., Jiang, D., Li, S., He, Z.-G., & Zhang, H. (2026) · Frontiers in Tuberculosis · doi:10.3389/ftubr.2026.1830528

A Construction of Archaean Rest-Like Biology from GenomicsPreprint

Vellanki, A. (2026) · Research Square · doi:10.21203/rs.3.rs-10315455/v1

MarR family proteins are important regulators of clinically relevant antibiotic resistance

Beggs, G. A., Brennan, R. G., & Arshad, M. (2019) · Protein Science · doi:10.1002/pro.3769 · Cited by 67

Function and Structure of MarR Family Members

Alekshun, M. N., & Head, J. W. (2014) · ASM Press eBooks · doi:10.1128/9781555817572.ch18 · Cited by 2

MarR family transcription factors: dynamic variations on a common scaffold

Deochand, D. K., & Grove, A. (2017) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2017.1344612 · Cited by 179

Genetic and functional analysis of the multiple antibiotic resistance (mar) locus in Escherichia coli

Cohen, S., Hächler, H., & Levy, S. B. (1993) · Journal of Bacteriology · doi:10.1128/jb.175.5.1484-1492.1993 · Cited by 392

The multiple antibiotic resistance operon of enteric bacteria controls DNA repair and outer membrane integrity

Sharma, P., Haycocks, J. R. J., Middlemiss, A. D., Kettles, R. A., Sellars, L. E., Ricci, V., Piddock, L. J. V., & Grainger, D. C. (2017) · Nature Communications · doi:10.1038/s41467-017-01405-7 · Cited by 134