Tau25A 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
1Tau25APO4-2.778receptor_Tau25A_10VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau25APO4-2.697receptor_Tau25A_1LEU-693 THR-694 PHE-695 ASN-698 ALA-699THR-694
3Tau25APO4-2.537receptor_Tau25A_11LYS-660 LEU-661 ASP-662 ASP-665 ARG-666
4Tau25APO4-2.458receptor_Tau25A_10VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
5Tau25APO4-2.447receptor_Tau25A_6ILE-734 ASP-735 MET-736 VAL-737 ASP-738 SER-739 LEU-742SER-739
6Tau25APO4-2.4receptor_Tau25A_10VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
7Tau25APO4-2.615receptor_Tau25A_10VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
8Tau25APO4-2.378receptor_Tau25A_6ILE-734 ASP-735 MET-736 VAL-737 ASP-738 SER-739 LEU-742SER-739
9Tau25APO4-2.364receptor_Tau25A_14LYS-692 LEU-693 THR-694 PHE-695 ARG-696 GLU-697 HIS-724 SER-726THR-694 SER-726