Resumen: Tuberculosis remains a critical global health challenge, which underscores the need for new therapeutic targets. A potential drug target is the rhodanese‐like thiosulfate sulfurtransferase SseA, which plays a role in macrophage infection by Mycobacterium tuberculosis (Mtb) and its resistance to oxidative stress. In our research, we identified a protein (Rv3284), herein referred to as SufEMtb, that interacts with SseA and modulates its activity. Sequence analysis and molecular modeling revealed that SufEMtb enhances SseA enzymatic function by binding to its non‐catalytic N‐terminal domain and favoring an activating conformational change in a regulatory loop of SseA. This interaction appears crucial for effective enzyme activity and the maintenance of redox homeostasis in Mtb, making the SseA–SufEMtb complex a potential target for new therapies. Idioma: Inglés DOI: 10.1002/1873-3468.70117 Año: 2025 Publicado en: FEBS Letters 599, 16 (2025), 2362-2376 ISSN: 0014-5793 Financiación: info:eu-repo/grantAgreement/ES/DGA-FEDER/E35-23R Financiación: info:eu-repo/grantAgreement/ES/MICINN/PID2022-136369NB-I00 Tipo y forma: Article (Published version) Área (Departamento): Área Bioquímica y Biolog.Mole. (Dpto. Bioq.Biolog.Mol. Celular)