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Molecular insights into RBR E3 ligase ubiquitin transfer mechanisms
journal contributionposted on 17.07.2020, 16:37 by Katja K Dove, Benjamin Stieglitz, Emily D Duncan, Katrin Rittinger, Rachel E Klevit
RING-in-between-RING (RBR) ubiquitin (Ub) ligases are a distinct class of E3s, defined by a RING1 domain that binds E2 Ub-conjugating enzyme and a RING2 domain that contains an active site cysteine similar to HECT-type E3s. Proposed to function as RING/HECT hybrids, details regarding the Ub transfer mechanism used by RBRs have yet to be defined. When paired with RING-type E3s, E2s perform the final step of Ub ligation to a substrate. In contrast, when paired with RBR E3s, E2s must transfer Ub onto the E3 to generate a E3~Ub intermediate. We show that RBRs utilize two strategies to ensure transfer of Ub from the E2 onto the E3 active site. First, RING1 domains of HHARI and RNF144 promote open E2~Ubs. Second, we identify a Ub-binding site on HHARI RING2 important for its recruitment to RING1-bound E2~Ub. Mutations that ablate Ub binding to HHARI RING2 also decrease RBR ligase activity, consistent with RING2 recruitment being a critical step for the RBR Ub transfer mechanism. Finally, we demonstrate that the mechanism defined here is utilized by a variety of RBRs.
HHARIHOIPParkinRBRubiquitin E3 ligaseBinding SitesCatalytic DomainHumansHydrophobic and Hydrophilic InteractionsModels, MolecularPolycomb Repressive Complex 1Protein BindingProtein ConformationProtein TransportTumor Suppressor ProteinsUbiquitinUbiquitin ThiolesteraseUbiquitin-Conjugating EnzymesUbiquitin-Protein LigasesUbiquitinationRittinger FC0011420601 Biochemistry and Cell BiologyDevelopmental Biology