9OLE
Crystal Structure of PI5P4KIIAlpha complex with 066ATZ
This is a non-PDB format compatible entry.
Summary for 9OLE
| Entry DOI | 10.2210/pdb9ole/pdb |
| Descriptor | Phosphatidylinositol 5-phosphate 4-kinase type-2 alpha, SULFATE ION, (7S)-8-cyclopentyl-5-methyl-7-[(pyridin-2-yl)methyl]-2-{[5-(1H-tetrazol-5-yl)-1,3-thiazol-2-yl]amino}-7,8-dihydropteridin-6(5H)-one, ... (4 entities in total) |
| Functional Keywords | kinase, transferase |
| Biological source | Homo sapiens (human) |
| Total number of polymer chains | 1 |
| Total formula weight | 43892.44 |
| Authors | |
| Primary citation | He, Z.,Chen, S.,Bosenberg, M.,Muthusamy, V.,Xi, Y.,Wang, H.,Micheli, F.,Cianciulli, A.,Beato, C.,Van Zandt, M.,Ellman, J.,Ha, Y. PIP4K2A/2B inhibitor suppresses tumor growth in a xenograft model of NSCLC. Iscience, 29:115952-115952, 2026 Cited by PubMed Abstract: The PIP4K family of lipid kinases phosphorylates the rare phospholipid PI(5)P at the 4-position, generating PI(4,5)P inside the cell. Although the functions of PIP4K, as well as the intracellular pools of PI(5)P and PI(4,5)P, remain incompletely understood, there are emerging interests in developing inhibitors to target these kinases since their genetic ablations have broad tumor-suppressive and other beneficial effects. Here, we report continued optimization of a previously discovered 2-amino-dihydropteridinone PIP4K2A/2B inhibitor and demonstrate, for the first time that pharmacological inhibition of PIP4K2A/2B suppresses solid tumor growth . The tumor-suppressive effect of the inhibitor appears to be non-tumor cell-autonomous and is likely mediated by components of the tumor microenvironment, including macrophages that commonly adopt alternatively activated states and support tumor growth. Our findings suggest a potential role for PIP4K activity in tumor-associated macrophages and provide a rationale for further exploring pharmacological targeting of these lipid kinases in cancer. PubMed: 42205699DOI: 10.1016/j.isci.2026.115952 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.404 Å) |
Structure validation
Download full validation report






