Tau22C 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
1Tau22CPO4-2.886receptor_Tau22C_12GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
2Tau22CPO4-2.771receptor_Tau22C_6LYS-700 ALA-701 THR-703 ASP-704 HIS-705 ALA-707THR-703
3Tau22CPO4-2.71receptor_Tau22C_9GLN-605 SER-606 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
4Tau22CPO4-2.628receptor_Tau22C_5ILE-734 ASP-735 MET-736 VAL-737 ASP-738 SER-739SER-739
5Tau22CPO4-2.386receptor_Tau22C_12GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
6Tau22CPO4-2.73receptor_Tau22C_12GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
7Tau22CPO4-2.692receptor_Tau22C_12GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
8Tau22CPO4-2.275receptor_Tau22C_9GLN-605 SER-606 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
9Tau22CPO4-2.428receptor_Tau22C_9GLN-605 SER-606 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610