Tau6A 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
1Tau6APO4-3.162receptor_Tau6A_12VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
2Tau6APO4-2.913receptor_Tau6A_14GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
3Tau6APO4-2.709receptor_Tau6A_3LEU-693 THR-694 PHE-695 ASN-698 ALA-699THR-694
4Tau6APO4-2.29receptor_Tau6A_12VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
5Tau6APO4-2.394receptor_Tau6A_12VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
6Tau6APO4-2.361receptor_Tau6A_12VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
7Tau6APO4-2.177receptor_Tau6A_14GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
8Tau6APO4-2.452receptor_Tau6A_14GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
9Tau6APO4-2.507receptor_Tau6A_14GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610