Tau16E 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
1Tau16EPO4-2.949receptor_Tau16E_1ARG-696 GLU-697 ALA-699 LYS-700 ALA-701 THR-703 GLY-706 ALA-707 GLU-708 ILE-709 TYR-711THR-703 TYR-711
2Tau16EPO4-2.72receptor_Tau16E_1ARG-696 GLU-697 ALA-699 LYS-700 ALA-701 THR-703 GLY-706 ALA-707 GLU-708 ILE-709 TYR-711THR-703 TYR-711
3Tau16EPO4-2.756receptor_Tau16E_1ARG-696 GLU-697 ALA-699 LYS-700 ALA-701 THR-703 GLY-706 ALA-707 GLU-708 ILE-709 TYR-711THR-703 TYR-711
4Tau16EPO4-3.069receptor_Tau16E_1ARG-696 GLU-697 ALA-699 LYS-700 ALA-701 THR-703 GLY-706 ALA-707 GLU-708 ILE-709 TYR-711THR-703 TYR-711
5Tau16EPO4-2.638receptor_Tau16E_1ARG-696 GLU-697 ALA-699 LYS-700 ALA-701 THR-703 GLY-706 ALA-707 GLU-708 ILE-709 TYR-711THR-703 TYR-711
6Tau16EPO4-2.626receptor_Tau16E_1ARG-696 GLU-697 ALA-699 LYS-700 ALA-701 THR-703 GLY-706 ALA-707 GLU-708 ILE-709 TYR-711THR-703 TYR-711
7Tau16EPO4-2.859receptor_Tau16E_1ARG-696 GLU-697 ALA-699 LYS-700 ALA-701 THR-703 GLY-706 ALA-707 GLU-708 ILE-709 TYR-711THR-703 TYR-711
8Tau16EPO4-2.834receptor_Tau16E_1ARG-696 GLU-697 ALA-699 LYS-700 ALA-701 THR-703 GLY-706 ALA-707 GLU-708 ILE-709 TYR-711THR-703 TYR-711
9Tau16EPO4-2.625receptor_Tau16E_13PHE-271 LEU-272 SER-273 LYS-274SER-273