Tau14C 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
1Tau14CPO4-3.12receptor_Tau14C_18GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau14CPO4-2.666receptor_Tau14C_13LYS-700 ALA-701 THR-703 ASP-704 HIS-705 ALA-707THR-703
3Tau14CPO4-2.514receptor_Tau14C_6LYS-692 LEU-693 THR-694 PHE-695 ASN-698THR-694
4Tau14CPO4-2.465receptor_Tau14C_3VAL-680 PRO-681 GLY-682 GLY-683 GLY-684 ASN-685 LYS-686 ILE-688
5Tau14CPO4-2.45receptor_Tau14C_3VAL-680 PRO-681 GLY-682 GLY-683 GLY-684 ASN-685 LYS-686 ILE-688
6Tau14CPO4-2.441receptor_Tau14C_1LEU-661 ASP-662 PHE-663 ASP-665 ARG-666 VAL-667
7Tau14CPO4-2.439receptor_Tau14C_18GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
8Tau14CPO4-2.448receptor_Tau14C_18GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
9Tau14CPO4-2.4receptor_Tau14C_5THR-30 MET-31 HIS-32 GLN-33 ASP-34THR-30