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9Q2D

Cryo-EM structure of ternary complex Ikaros-ZF2:CC-885:CRBN:DDB1 (molecular glue degrader)

Summary for 9Q2D
Entry DOI10.2210/pdb9q2d/pdb
Related9Q22
EMDB information72160
DescriptorDNA-binding protein Ikaros, Protein cereblon, DNA damage-binding protein 1, ... (5 entities in total)
Functional Keywordscereblon, degrader, ikaros, ikzf1, ddb1, molecular glue, ligase
Biological sourceHomo sapiens (human)
More
Total number of polymer chains3
Total formula weight157232.19
Authors
Zhu, J.,Pagarigan, B.E.,Tran, E.T. (deposition date: 2025-08-15, release date: 2025-10-01)
Primary citationLuchini, G.,Liu, S.,Powers, H.L.,Cherney, E.,Zhu, J.,Danga, K.,Thompson, J.W.,Shi, L.,Pagarigan, B.,Wei, D.D.,Park, P.,Degnan, A.P.,Zapf, C.W.,Riggs, J.R.,Johnson, S.,Cummins, T.
Application of Weighted Interaction-Fingerprints for Rationalizing Neosubstrate Potency and Selectivity of Cereblon-Based Molecular Glues.
J.Med.Chem., 2025
Cited by
PubMed Abstract: Cullin-RING Ligase 4 Cereblon (CRL4) (CRBN) E3 ligase modulatory drugs (CELMoDs) make up a successful class of compounds targeting neosubstrates for proteasome-dependent degradation. Early immunomodulatory drugs (IMiDs) target Ikaros and Aiolos degradation. In addition, there are ongoing clinical trials targeting the degradation of biologically relevant proteins such as GSPT1, CK1α, and Helios with CRBN-based molecular glues. To date, most advanced preclinical and clinical CRBN-based molecular glues recruit their neosubstrates through canonical G-motifs, secondary protein features that are structurally similar but have significantly different amino acid sequence identities. Analogous to the development of kinase inhibitors, optimizing both neosubstrate recruitment and degradation selectivity is important to minimize potential off-target activity. Here, we describe a computational structure-based approach to analyze and predict putative ligand interactions important in the neosubstrate ternary complex. This approach provides valuable insights for enhanced designs toward the development of more selective and efficacious CRBN-based molecular glues.
PubMed: 40994183
DOI: 10.1021/acs.jmedchem.5c01919
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.94 Å)
Structure validation

242842

数据于2025-10-08公开中

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