Tau24A 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
1Tau24APO4-3.077receptor_Tau24A_11GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau24APO4-3.01receptor_Tau24A_20ALA-701 THR-703 ASP-704 HIS-705 ALA-707 ILE-709THR-703
3Tau24APO4-2.98receptor_Tau24A_22VAL-667 GLN-668 SER-669 ILE-671 GLY-672 SER-673 LEU-674 ASP-675SER-669 SER-673
4Tau24APO4-2.706receptor_Tau24A_9VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
5Tau24APO4-2.616receptor_Tau24A_9VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
6Tau24APO4-2.596receptor_Tau24A_18ARG-696 GLU-697 ALA-699 LYS-700 ALA-701 ILE-709 TYR-711TYR-711
7Tau24APO4-2.541receptor_Tau24A_18ARG-696 GLU-697 ALA-699 LYS-700 ALA-701 ILE-709 TYR-711TYR-711
8Tau24APO4-2.897receptor_Tau24A_20ALA-701 THR-703 ASP-704 HIS-705 ALA-707 ILE-709THR-703
9Tau24APO4-2.845receptor_Tau24A_18ARG-696 GLU-697 ALA-699 LYS-700 ALA-701 ILE-709 TYR-711TYR-711