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    <subfield code="a">10.1002/1873-3468.70117</subfield>
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    <subfield code="a">Di Napoli, Giulia</subfield>
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    <subfield code="a">Mycobacterium tuberculosis sulfurtransferase SseA is activated by its neighboring gene product Rv3284</subfield>
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    <subfield code="c">2025</subfield>
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    <subfield code="a">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.</subfield>
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    <subfield code="a">Fissore, Alex</subfield>
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    <subfield code="a">Salladini, Edoardo</subfield>
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    <subfield code="a">Raccuia, Eleonora</subfield>
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    <subfield code="a">Oliaro-Bosso, Simonetta</subfield>
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    <subfield code="a">Medina, Milagros</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-8743-0182</subfield>
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    <subfield code="a">Velazquez-Campoy, Adrian</subfield>
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    <subfield code="a">Adinolfi, Salvatore</subfield>
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    <subfield code="1">1002</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Bioq.Biolog.Mol. Celular</subfield>
    <subfield code="c">Área Bioquímica y Biolog.Mole.</subfield>
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    <subfield code="g">599, 16 (2025), 2362-2376</subfield>
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    <subfield code="t">FEBS Letters</subfield>
    <subfield code="x">0014-5793</subfield>
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