Tau10E 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
1Tau10EPO4-3.285receptor_Tau10E_12VAL-604 GLN-605 SER-606 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau10EPO4-2.771receptor_Tau10E_9ALA-701 THR-703 ASP-704 HIS-705 ALA-707 ILE-709THR-703
3Tau10EPO4-2.645receptor_Tau10E_8ASP-270 PHE-271 LEU-272 SER-273SER-273
4Tau10EPO4-2.572receptor_Tau10E_4PHE-271 LEU-272 SER-273 LYS-274 VAL-275SER-273
5Tau10EPO4-2.491receptor_Tau10E_8ASP-270 PHE-271 LEU-272 SER-273SER-273
6Tau10EPO4-2.416receptor_Tau10E_10ILE-734 ASP-735 MET-736 VAL-737 ASP-738 SER-739 LEU-742SER-739
7Tau10EPO4-2.694receptor_Tau10E_10ILE-734 ASP-735 MET-736 VAL-737 ASP-738 SER-739 LEU-742SER-739
8Tau10EPO4-2.399receptor_Tau10E_10ILE-734 ASP-735 MET-736 VAL-737 ASP-738 SER-739 LEU-742SER-739
9Tau10EPO4-2.331receptor_Tau10E_12VAL-604 GLN-605 SER-606 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610