Tau22A 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
1Tau22APO4-2.951receptor_Tau22A_13GLN-668 SER-669 LYS-670 ILE-671 GLY-672 LEU-674 ASP-675SER-669
2Tau22APO4-2.836receptor_Tau22A_1LYS-700 ALA-701 LYS-702 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 GLU-708 ILE-709THR-703
3Tau22APO4-2.734receptor_Tau22A_6GLN-605 SER-606 LYS-607 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
4Tau22APO4-2.658receptor_Tau22A_12VAL-573 LYS-574 SER-575 ILE-577 GLY-578 THR-580 GLU-581SER-575 THR-580
5Tau22APO4-2.623receptor_Tau22A_6GLN-605 SER-606 LYS-607 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
6Tau22APO4-2.505receptor_Tau22A_13GLN-668 SER-669 LYS-670 ILE-671 GLY-672 LEU-674 ASP-675SER-669
7Tau22APO4-2.737receptor_Tau22A_13GLN-668 SER-669 LYS-670 ILE-671 GLY-672 LEU-674 ASP-675SER-669
8Tau22APO4-2.462receptor_Tau22A_6GLN-605 SER-606 LYS-607 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
9Tau22APO4-2.441receptor_Tau22A_1LYS-700 ALA-701 LYS-702 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 GLU-708 ILE-709THR-703