Tau15D phosphorylation.     


AI Overview (Google's Gemini, March 26, 2026)

Yes, multiple phosphate (PO4) molecules can bind within the same functional regions or "pockets" of the tau protein, particularly in cases of hyperphosphorylation associated with Alzheimer’s disease. In summary, the high concentration of potential sites in specific domains makes it likely that multiple phosphate groups reside in the same or closely positioned areas, directly causing the conformational changes that lead to pathology.


       
       



Order of bindingReceptorLigandAffinityPocket IDResidues that formed the binding pocketPresence of SER, THR, TYR
1Tau15DPO4-3.126receptor_Tau15D_4SER-602 VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-602 SER-606 SER-610
2Tau15DPO4-2.805receptor_Tau15D_16ALA-701 THR-703 ASP-704 HIS-705 ALA-707 ILE-709THR-703
3Tau15DPO4-2.724receptor_Tau15D_15VAL-573 LYS-574 SER-575 ILE-577 GLY-578 THR-580 GLU-581SER-575 THR-580
4Tau15DPO4-2.33receptor_Tau15D_4SER-602 VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-602 SER-606 SER-610
5Tau15DPO4-2.518receptor_Tau15D_4SER-602 VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-602 SER-606 SER-610
6Tau15DPO4-2.345receptor_Tau15D_12LYS-598 LEU-599 ASP-600 LEU-601
7Tau15DPO4-2.284receptor_Tau15D_4SER-602 VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-602 SER-606 SER-610
8Tau15DPO4-2.623receptor_Tau15D_4SER-602 VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-602 SER-606 SER-610
9Tau15DPO4-2.28receptor_Tau15D_15VAL-573 LYS-574 SER-575 ILE-577 GLY-578 THR-580 GLU-581SER-575 THR-580