8OG6
Crystal structure of human DCAF1 WD40 repeats (Q1250L) in complex with compound 1
Summary for 8OG6
Entry DOI | 10.2210/pdb8og6/pdb |
Related | 8OG5 |
Descriptor | DDB1- and CUL4-associated factor 1, 5-(2-fluorophenyl)-2,3-dihydroimidazo[2,1-a]isoquinoline, ACETATE ION, ... (4 entities in total) |
Functional Keywords | dcaf1, e3 ligase, compound, transferase |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 42352.46 |
Authors | Schroeder, M.,Vulpetti, A.,Renatus, M. (deposition date: 2023-03-19, release date: 2023-06-14, Last modification date: 2024-06-19) |
Primary citation | Vulpetti, A.,Holzer, P.,Schmiedeberg, N.,Imbach-Weese, P.,Pissot-Soldermann, C.,Hollingworth, G.J.,Radimerski, T.,Thoma, C.R.,Stachyra, T.M.,Wojtynek, M.,Maschlej, M.,Chau, S.,Schuffenhauer, A.,Fernandez, C.,Schroder, M.,Renatus, M. Discovery of New Binders for DCAF1, an Emerging Ligase Target in the Targeted Protein Degradation Field. Acs Med.Chem.Lett., 14:949-954, 2023 Cited by PubMed Abstract: In this study, we describe the rapid identification of potent binders for the WD40 repeat domain (WDR) of DCAF1. This was achieved by two rounds of iterative focused screening of a small set of compounds selected on the basis of internal WDR domain knowledge followed by hit expansion. Subsequent structure-based design led to nanomolar potency binders with a clear exit vector enabling DCAF1-based bifunctional degrader exploration. PubMed: 37465299DOI: 10.1021/acsmedchemlett.3c00104 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.245 Å) |
Structure validation
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