Tau11C 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
1Tau11CPO4-2.978receptor_Tau11C_7VAL-604 GLN-605 SER-606 CYS-608 GLY-609 LYS-611 ASP-612SER-606
2Tau11CPO4-2.961receptor_Tau11C_5VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
3Tau11CPO4-2.678receptor_Tau11C_1LEU-693 THR-694 PHE-695 ASN-698 ALA-699THR-694
4Tau11CPO4-2.611receptor_Tau11C_5VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
5Tau11CPO4-2.547receptor_Tau11C_6ILE-734 ASP-735 MET-736 VAL-737 SER-739 GLN-741 LEU-742SER-739
6Tau11CPO4-2.286receptor_Tau11C_1LEU-693 THR-694 PHE-695 ASN-698 ALA-699THR-694
7Tau11CPO4-2.271receptor_Tau11C_7VAL-604 GLN-605 SER-606 CYS-608 GLY-609 LYS-611 ASP-612SER-606
8Tau11CPO4-2.235receptor_Tau11C_7VAL-604 GLN-605 SER-606 CYS-608 GLY-609 LYS-611 ASP-612SER-606
9Tau11CPO4-2.41receptor_Tau11C_7VAL-604 GLN-605 SER-606 CYS-608 GLY-609 LYS-611 ASP-612SER-606