4TYL
Fragment-Based Screening of the Bromodomain of ATAD2
Summary for 4TYL
Entry DOI | 10.2210/pdb4tyl/pdb |
Related | 4TZ2 4TZ8 |
Descriptor | ATPase family AAA domain-containing protein 2, SULFATE ION, CHLORIDE ION, ... (5 entities in total) |
Functional Keywords | bromodomain, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 1 |
Total formula weight | 15882.62 |
Authors | Harner, M.J.,Chauder, B.A.,Phan, J.,Fesik, S.W. (deposition date: 2014-07-08, release date: 2014-10-29, Last modification date: 2023-12-27) |
Primary citation | Harner, M.J.,Chauder, B.A.,Phan, J.,Fesik, S.W. Fragment-Based Screening of the Bromodomain of ATAD2. J.Med.Chem., 57:9687-9692, 2014 Cited by PubMed Abstract: Cellular and genetic evidence suggest that inhibition of ATAD2 could be a useful strategy to treat several types of cancer. To discover small-molecule inhibitors of the bromodomain of ATAD2, we used a fragment-based approach. Fragment hits were identified using NMR spectroscopy, and ATAD2 was crystallized with three of the hits identified in the fragment screen. PubMed: 25314628DOI: 10.1021/jm501035j PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.85 Å) |
Structure validation
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