1I7E
C-Terminal Domain Of Mouse Brain Tubby Protein bound to Phosphatidylinositol 4,5-bis-phosphate
Summary for 1I7E
Entry DOI | 10.2210/pdb1i7e/pdb |
Related | 1C8Z |
Descriptor | TUBBY PROTEIN, L-ALPHA-GLYCEROPHOSPHO-D-MYO-INOSITOL-4,5-BIS-PHOSPHATE (3 entities in total) |
Functional Keywords | tubby filled-barrel beta-barrel filled-beta-roll 12-stranded-beta-barrel helix-filled-barrel obesity blindness deafness phosphoinositide phosphatidylinositol, signaling protein |
Biological source | Mus musculus (house mouse) |
Cellular location | Cytoplasm: P50586 |
Total number of polymer chains | 1 |
Total formula weight | 30489.35 |
Authors | Santagata, S.,Boggon, T.J.,Baird, C.L.,Shan, W.S.,Shapiro, L. (deposition date: 2001-03-08, release date: 2001-06-27, Last modification date: 2023-08-09) |
Primary citation | Santagata, S.,Boggon, T.J.,Baird, C.L.,Gomez, C.A.,Zhao, J.,Shan, W.S.,Myszka, D.G.,Shapiro, L. G-protein signaling through tubby proteins. Science, 292:2041-2050, 2001 Cited by PubMed Abstract: Dysfunction of the tubby protein results in maturity-onset obesity in mice. Tubby has been implicated as a transcription regulator, but details of the molecular mechanism underlying its function remain unclear. Here we show that tubby functions in signal transduction from heterotrimeric GTP-binding protein (G protein)-coupled receptors. Tubby localizes to the plasma membrane by binding phosphatidylinositol 4,5-bisphosphate through its carboxyl terminal "tubby domain." X-ray crystallography reveals the atomic-level basis of this interaction and implicates tubby domains as phosphorylated-phosphatidyl- inositol binding factors. Receptor-mediated activation of G protein alphaq (Galphaq) releases tubby from the plasma membrane through the action of phospholipase C-beta, triggering translocation of tubby to the cell nucleus. The localization of tubby-like protein 3 (TULP3) is similarly regulated. These data suggest that tubby proteins function as membrane-bound transcription regulators that translocate to the nucleus in response to phosphoinositide hydrolysis, providing a direct link between G-protein signaling and the regulation of gene expression. PubMed: 11375483DOI: 10.1126/science.1061233 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.95 Å) |
Structure validation
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