Tau2A 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
1Tau2APO4-2.777receptor_Tau2A_2VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau2APO4-2.597receptor_Tau2A_1ILE-734 MET-736 VAL-737 ASP-738 SER-739 PRO-740 LEU-742 ALA-743SER-739
3Tau2APO4-2.403receptor_Tau2A_6LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707THR-703
4Tau2APO4-2.355receptor_Tau2A_4VAL-667 GLN-668 SER-669 GLY-672 SER-673 LEU-674 ASP-675SER-669 SER-673
5Tau2APO4-2.34receptor_Tau2A_1ILE-734 MET-736 VAL-737 ASP-738 SER-739 PRO-740 LEU-742 ALA-743SER-739
6Tau2APO4-2.326receptor_Tau2A_2VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
7Tau2APO4-2.306receptor_Tau2A_2VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
8Tau2APO4-2.387receptor_Tau2A_2VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
9Tau2APO4-2.3receptor_Tau2A_1ILE-734 MET-736 VAL-737 ASP-738 SER-739 PRO-740 LEU-742 ALA-743SER-739