Tau8C 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
1Tau8CPO4-3.142receptor_Tau8C_6VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau8CPO4-2.931receptor_Tau8C_14LYS-700 ALA-701 THR-703 ASP-704 HIS-705 ALA-707 ILE-709THR-703
3Tau8CPO4-2.901receptor_Tau8C_16GLN-668 SER-669 ILE-671 GLY-672 SER-673 LEU-674 ASP-675SER-669 SER-673
4Tau8CPO4-2.65receptor_Tau8C_13ASP-270 PHE-271 LEU-272 SER-273SER-273
5Tau8CPO4-2.634receptor_Tau8C_18VAL-573 LYS-574 SER-575 ILE-577 GLY-578 THR-580 GLU-581SER-575 THR-580
6Tau8CPO4-2.536receptor_Tau8C_12LYS-692 LEU-693 THR-694 PHE-695 ASN-698THR-694
7Tau8CPO4-2.493receptor_Tau8C_13ASP-270 PHE-271 LEU-272 SER-273SER-273
8Tau8CPO4-2.437receptor_Tau8C_14LYS-700 ALA-701 THR-703 ASP-704 HIS-705 ALA-707 ILE-709THR-703
9Tau8CPO4-2.579receptor_Tau8C_3LYS-692 LEU-693 THR-694 PHE-695 ARG-696 GLU-697 ILE-709 TYR-711THR-694 TYR-711