9Q22
Crystal structure of ternary complex Helios-ZF2:I-19:CRBN:DDB1
This is a non-PDB format compatible entry.
Summary for 9Q22
| Entry DOI | 10.2210/pdb9q22/pdb |
| Descriptor | DNA damage-binding protein 1, Protein cereblon, Zinc finger protein Helios, ... (5 entities in total) |
| Functional Keywords | cereblon, degrader, helios, ikzf2, ddb1, moclecular glue, ligase |
| Biological source | Homo sapiens (human) More |
| Total number of polymer chains | 3 |
| Total formula weight | 148746.02 |
| Authors | Zhu, J.,Pagarigan, B.E.,Tran, E.T. (deposition date: 2025-08-14, release date: 2025-10-01, Last modification date: 2025-10-22) |
| Primary citation | Luchini, 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., 68:20657-20674, 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: 40994183DOI: 10.1021/acs.jmedchem.5c01919 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (3.406 Å) |
Structure validation
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