6Q6Y
PI3K delta in complex with N(2chloro5phenylpyridin3yl)benzenesulfonamide
Summary for 6Q6Y
| Entry DOI | 10.2210/pdb6q6y/pdb |
| Descriptor | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform, ~{N}-(2-chloranyl-5-phenyl-pyridin-3-yl)benzenesulfonamide (3 entities in total) |
| Functional Keywords | pi3 kinase delta, complex, structure based design, transferase |
| Biological source | Mus musculus (House mouse) |
| Total number of polymer chains | 1 |
| Total formula weight | 108168.48 |
| Authors | Convery, M.A.,Rowland, P.,Down, K.,Barton, N. (deposition date: 2018-12-12, release date: 2018-12-26, Last modification date: 2024-06-19) |
| Primary citation | Barton, N.,Convery, M.,Cooper, A.W.J.,Down, K.,Hamblin, J.N.,Inglis, G.,Peace, S.,Rowedder, J.,Rowland, P.,Taylor, J.A.,Wellaway, N. Discovery of Potent, Efficient, and Selective Inhibitors of Phosphoinositide 3-Kinase delta through a Deconstruction and Regrowth Approach. J.Med.Chem., 61:11061-11073, 2018 Cited by PubMed Abstract: A deconstruction of previously reported phosphoinositide 3-kinase δ (PI3Kδ) inhibitors and subsequent regrowth led to the identification of a privileged fragment for PI3Kδ, which was exploited to deliver a potent, efficient, and selective lead series with a novel binding mode observed in the PI3Kδ crystal structure. PubMed: 30532965DOI: 10.1021/acs.jmedchem.8b01556 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.03 Å) |
Structure validation
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