{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Du J"],"funding":["Deutsche Forschungsgemeinschaft (DFG)","European Molecular Biology Organization (EMBO)","Max Planck Society","Boehringer Ingelheim Fonds (BIF)"],"pagination":["e2524899122"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12773759"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["123(1)"],"pubmed_abstract":["E3 ligases partner with E2 enzymes to regulate vast eukaryotic biology. The hierarchical nature of these pairings, with >600 E3s and ~40 E2s in humans, necessitates that E2s cofunction with numerous different E3s. Here, focusing on E3s in the RING-between-RING (RBR) family and their partner UBE2L3 and UBE2D-family E2s, we report an approach to interrogate selected pathways. We screened phage-displayed libraries of structure-based E2 variants (E2Vs) to discover enzymes with enhanced affinity and specificity toward half of all RBR E3 ligases (ARIH1, ARIH2, ANKIB1, CUL9, HOIL1, HOIP, and RNF14). Collectively, these E2Vs allowed distinguishing actions of different cofunctioning E3s, obtaining high-resolution cryogenic Electron Microscopy (cryo-EM) structures of an RBR E3 in the context of a su"],"journal":["Proceedings of the National Academy of Sciences of the United States of America"],"pubmed_title":["E2 variants for probing E3 ubiquitin ligase activities."],"pmcid":["PMC12773759"],"funding_grant_id":["ALTF 627-2022","Schulman Department","PhD Fellowship","SCH3196/1-1","Mann Department"],"pubmed_authors":["Singh J","Kiss L","Sidhu SS","Andree GA","Schulman BA","Horn-Ghetko D","Du J","Kostrhon S","Mann M","Stier L"],"additional_accession":[]},"is_claimable":false,"name":"E2 variants for probing E3 ubiquitin ligase activities.","description":"E3 ligases partner with E2 enzymes to regulate vast eukaryotic biology. The hierarchical nature of these pairings, with >600 E3s and ~40 E2s in humans, necessitates that E2s cofunction with numerous different E3s. Here, focusing on E3s in the RING-between-RING (RBR) family and their partner UBE2L3 and UBE2D-family E2s, we report an approach to interrogate selected pathways. We screened phage-displayed libraries of structure-based E2 variants (E2Vs) to discover enzymes with enhanced affinity and specificity toward half of all RBR E3 ligases (ARIH1, ARIH2, ANKIB1, CUL9, HOIL1, HOIP, and RNF14). Collectively, these E2Vs allowed distinguishing actions of different cofunctioning E3s, obtaining high-resolution cryogenic Electron Microscopy (cryo-EM) structures of an RBR E3 in the context of a su","dates":{"release":"2026-01-01T00:00:00Z","publication":"2026 Jan","modification":"2026-06-06T11:08:10.562Z","creation":"2026-05-29T03:12:42.794Z"},"accession":"S-EPMC12773759","cross_references":{"pubmed":["41481455"],"doi":["10.1073/pnas.2524899122"]}}