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8TNR

Cryo-EM structure of DDB1dB:CRBN:PT-179:SD40, conformation 2

Summary for 8TNR
Entry DOI10.2210/pdb8tnr/pdb
EMDB information41423 41424 41425
DescriptorDNA damage-binding protein 1, Protein cereblon, Maltose/maltodextrin-binding periplasmic protein,SD40, ... (5 entities in total)
Functional Keywordsubiquitin, crbn, directed evolution, zinc finger, imid, molecular glue, transferase
Biological sourceHomo sapiens (human)
More
Total number of polymer chains3
Total formula weight202118.70
Authors
Roy Burman, S.S.,Hunkeler, M.,Fischer, E.S. (deposition date: 2023-08-02, release date: 2024-03-13, Last modification date: 2024-04-03)
Primary citationMercer, J.A.M.,DeCarlo, S.J.,Roy Burman, S.S.,Sreekanth, V.,Nelson, A.T.,Hunkeler, M.,Chen, P.J.,Donovan, K.A.,Kokkonda, P.,Tiwari, P.K.,Shoba, V.M.,Deb, A.,Choudhary, A.,Fischer, E.S.,Liu, D.R.
Continuous evolution of compact protein degradation tags regulated by selective molecular glues.
Science, 383:eadk4422-eadk4422, 2024
Cited by
PubMed Abstract: Conditional protein degradation tags (degrons) are usually >100 amino acids long or are triggered by small molecules with substantial off-target effects, thwarting their use as specific modulators of endogenous protein levels. We developed a phage-assisted continuous evolution platform for molecular glue complexes (MG-PACE) and evolved a 36-amino acid zinc finger (ZF) degron (SD40) that binds the ubiquitin ligase substrate receptor cereblon in complex with PT-179, an orthogonal thalidomide derivative. Endogenous proteins tagged in-frame with SD40 using prime editing are degraded by otherwise inert PT-179. Cryo-electron microscopy structures of SD40 in complex with ligand-bound cereblon revealed mechanistic insights into the molecular basis of SD40's activity and specificity. Our efforts establish a system for continuous evolution of molecular glue complexes and provide ZF tags that overcome shortcomings associated with existing degrons.
PubMed: 38484051
DOI: 10.1126/science.adk4422
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.5 Å)
Structure validation

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PDB entries from 2024-11-13

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