Tau16D 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
1Tau16DPO4-2.929receptor_Tau16D_3ALA-699 LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 GLU-708 ILE-709THR-703
2Tau16DPO4-2.918receptor_Tau16D_16VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
3Tau16DPO4-2.906receptor_Tau16D_1VAL-604 GLN-605 SER-606 LYS-607 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
4Tau16DPO4-2.476receptor_Tau16D_3ALA-699 LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 GLU-708 ILE-709THR-703
5Tau16DPO4-2.507receptor_Tau16D_3ALA-699 LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 GLU-708 ILE-709THR-703
6Tau16DPO4-2.367receptor_Tau16D_16VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
7Tau16DPO4-2.649receptor_Tau16D_16VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
8Tau16DPO4-2.722receptor_Tau16D_16VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
9Tau16DPO4-2.305receptor_Tau16D_3ALA-699 LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 GLU-708 ILE-709THR-703