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UFC1 reveals the multifactorial and plastic nature of oxyanion holes in E2 conjugating enzymes

Author

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  • Manoj Kumar

    (Hebrew University-Hadassah Medical School)

  • Sayanika Banerjee

    (Hebrew University-Hadassah Medical School)

  • Einav Cohen-Kfir

    (Hebrew University-Hadassah Medical School)

  • Marissa Basia Mitelberg

    (Hebrew University-Hadassah Medical School)

  • Suryakant Tiwari

    (Bar-Ilan University)

  • Michail N. Isupov

    (University of Exeter)

  • Moshe Dessau

    (Bar-Ilan University)

  • Reuven Wiener

    (Hebrew University-Hadassah Medical School)

Abstract

The conjugation of ubiquitin (Ub) or ubiquitin-like proteins (UBL) to target proteins is a crucial post-translational modification that typically involves nucleophilic attack by a lysine on a charged E2 enzyme (E2~Ub/UBL), forming an oxyanion intermediate. Stabilizing this intermediate through an oxyanion hole is vital for progression of the reaction. Still, the mechanism of oxyanion stabilization in E2 enzymes remains unclear, although an asparagine residue in the conserved HPN motif of E2 enzymes was suggested to stabilize the oxyanion intermediate. Here, we study the E2 enzyme UFC1, which presents a TAK rather than an HPN motif. Crystal structures of UFC1 mutants, including one that mimics the oxyanion intermediate, combined with in vitro activity assays, suggest that UFC1 utilizes two distinct types of oxyanion holes, one that stabilizes the oxyanion intermediate during trans-ufmylation mediated by the E3 ligase, and another that stabilizes cis-driven auto-ufmylation. Our findings indicate that oxyanion stabilization is influenced by multiple factors, including C-alpha hydrogen bonding, and is adaptable, enabling different modes of action.

Suggested Citation

  • Manoj Kumar & Sayanika Banerjee & Einav Cohen-Kfir & Marissa Basia Mitelberg & Suryakant Tiwari & Michail N. Isupov & Moshe Dessau & Reuven Wiener, 2025. "UFC1 reveals the multifactorial and plastic nature of oxyanion holes in E2 conjugating enzymes," Nature Communications, Nature, vol. 16(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-58826-y
    DOI: 10.1038/s41467-025-58826-y
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    References listed on IDEAS

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    1. Linda Makhlouf & Joshua J. Peter & Helge M. Magnussen & Rohan Thakur & David Millrine & Thomas C. Minshull & Grace Harrison & Joby Varghese & Frederic Lamoliatte & Martina Foglizzo & Thomas Macartney , 2024. "The UFM1 E3 ligase recognizes and releases 60S ribosomes from ER translocons," Nature, Nature, vol. 627(8003), pages 437-444, March.
    2. Emma Branigan & J. Carlos Penedo & Ronald T. Hay, 2020. "Ubiquitin transfer by a RING E3 ligase occurs from a closed E2~ubiquitin conformation," Nature Communications, Nature, vol. 11(1), pages 1-11, December.
    3. Mark Hochstrasser, 2009. "Origin and function of ubiquitin-like proteins," Nature, Nature, vol. 458(7237), pages 422-429, March.
    4. Manoj Kumar & Prasanth Padala & Jamal Fahoum & Fouad Hassouna & Tomer Tsaban & Guy Zoltsman & Sayanika Banerjee & Einav Cohen-Kfir & Moshe Dessau & Rina Rosenzweig & Michail N. Isupov & Ora Schueler-F, 2021. "Structural basis for UFM1 transfer from UBA5 to UFC1," Nature Communications, Nature, vol. 12(1), pages 1-13, December.
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