Tau20C 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
1Tau20CPO4-2.769receptor_Tau20C_1LEU-693 THR-694 PHE-695 ASN-698 ALA-699THR-694
2Tau20CPO4-2.65receptor_Tau20C_7VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274 VAL-275SER-273
3Tau20CPO4-2.707receptor_Tau20C_7VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274 VAL-275SER-273
4Tau20CPO4-2.629receptor_Tau20C_13VAL-573 LYS-574 SER-575 GLY-578 THR-580 GLU-581SER-575 THR-580
5Tau20CPO4-2.516receptor_Tau20C_7VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274 VAL-275SER-273
6Tau20CPO4-2.514receptor_Tau20C_11VAL-667 GLN-668 SER-669 GLY-672 LEU-674 ASP-675SER-669
7Tau20CPO4-2.455receptor_Tau20C_10ILE-734 ASP-735 MET-736 VAL-737 ASP-738 SER-739SER-739
8Tau20CPO4-2.334receptor_Tau20C_11VAL-667 GLN-668 SER-669 GLY-672 LEU-674 ASP-675SER-669
9Tau20CPO4-2.332receptor_Tau20C_7VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274 VAL-275SER-273