Tau2B 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
1Tau2BPO4-2.711receptor_Tau2B_11VAL-604 GLN-605 SER-606 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau2BPO4-2.594receptor_Tau2B_16ILE-734 ASP-735 MET-736 ASP-738 SER-739 LEU-742SER-739
3Tau2BPO4-2.561receptor_Tau2B_2VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
4Tau2BPO4-2.618receptor_Tau2B_2VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
5Tau2BPO4-2.469receptor_Tau2B_1LEU-693 THR-694 PHE-695 ASN-698THR-694
6Tau2BPO4-2.433receptor_Tau2B_2VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
7Tau2BPO4-2.391receptor_Tau2B_16ILE-734 ASP-735 MET-736 ASP-738 SER-739 LEU-742SER-739
8Tau2BPO4-2.372receptor_Tau2B_11VAL-604 GLN-605 SER-606 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
9Tau2BPO4-2.434receptor_Tau2B_11VAL-604 GLN-605 SER-606 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610