Tau15C 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
1Tau15CPO4-3.033receptor_Tau15C_4VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau15CPO4-2.813receptor_Tau15C_2ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 GLU-708THR-703
3Tau15CPO4-2.67receptor_Tau15C_13ASP-270 PHE-271 LEU-272 SER-273SER-273
4Tau15CPO4-2.482receptor_Tau15C_1LEU-693 THR-694 PHE-695 ASN-698 ALA-699THR-694
5Tau15CPO4-2.465receptor_Tau15C_9LYS-660 LEU-661 ASP-662 ASP-665 ARG-666
6Tau15CPO4-2.453receptor_Tau15C_14VAL-667 GLN-668 SER-669 GLY-672 SER-673 LEU-674 ASP-675SER-669 SER-673
7Tau15CPO4-2.405receptor_Tau15C_12VAL-635 THR-636 SER-637 GLY-640 SER-641 LEU-642THR-636 SER-637 SER-641
8Tau15CPO4-2.245receptor_Tau15C_4VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
9Tau15CPO4-2.473receptor_Tau15C_4VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610