Tau10D 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
1Tau10DPO4-3.091receptor_Tau10D_5VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau10DPO4-2.758receptor_Tau10D_2LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 GLU-708THR-703
3Tau10DPO4-2.588receptor_Tau10D_2LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 GLU-708THR-703
4Tau10DPO4-2.585receptor_Tau10D_8ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
5Tau10DPO4-2.534receptor_Tau10D_7MET-736 VAL-737 ASP-738 SER-739 PRO-740 LEU-742SER-739
6Tau10DPO4-2.431receptor_Tau10D_3LEU-272 SER-273 LYS-274 VAL-275 SER-276SER-273 SER-276
7Tau10DPO4-2.425receptor_Tau10D_20GLN-668 SER-669 GLY-672 LEU-674 ASP-675SER-669
8Tau10DPO4-2.415receptor_Tau10D_21VAL-573 LYS-574 SER-575 GLY-578 THR-580 GLU-581SER-575 THR-580
9Tau10DPO4-2.379receptor_Tau10D_3LEU-272 SER-273 LYS-274 VAL-275 SER-276SER-273 SER-276