Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

8OG6

Crystal structure of human DCAF1 WD40 repeats (Q1250L) in complex with compound 1

Summary for 8OG6
Entry DOI10.2210/pdb8og6/pdb
Related8OG5
DescriptorDDB1- and CUL4-associated factor 1, 5-(2-fluorophenyl)-2,3-dihydroimidazo[2,1-a]isoquinoline, ACETATE ION, ... (4 entities in total)
Functional Keywordsdcaf1, e3 ligase, compound, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight42352.46
Authors
Schroeder, M.,Vulpetti, A.,Renatus, M. (deposition date: 2023-03-19, release date: 2023-06-14, Last modification date: 2024-06-19)
Primary citationVulpetti, 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: 37465299
DOI: 10.1021/acsmedchemlett.3c00104
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.245 Å)
Structure validation

226707

数据于2024-10-30公开中

PDB statisticsPDBj update infoContact PDBjnumon