Tau11E 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
1Tau11EPO4-3.007receptor_Tau11E_15ALA-699 LYS-700 ALA-701 THR-703 ASP-704 HIS-705 ALA-707 ILE-709THR-703
2Tau11EPO4-2.828receptor_Tau11E_11LEU-693 THR-694 PHE-695 ASN-698THR-694
3Tau11EPO4-2.675receptor_Tau11E_1ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
4Tau11EPO4-2.671receptor_Tau11E_17VAL-604 GLN-605 SER-606 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
5Tau11EPO4-2.517receptor_Tau11E_15ALA-699 LYS-700 ALA-701 THR-703 ASP-704 HIS-705 ALA-707 ILE-709THR-703
6Tau11EPO4-2.584receptor_Tau11E_15ALA-699 LYS-700 ALA-701 THR-703 ASP-704 HIS-705 ALA-707 ILE-709THR-703
7Tau11EPO4-2.484receptor_Tau11E_1ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
8Tau11EPO4-2.606receptor_Tau11E_1ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
9Tau11EPO4-2.482receptor_Tau11E_16VAL-573 LYS-574 SER-575 GLY-578 THR-580 GLU-581SER-575 THR-580