Tau13A 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
1Tau13APO4-3.076receptor_Tau13A_5GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau13APO4-2.889receptor_Tau13A_15ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 ILE-709THR-703
3Tau13APO4-2.539receptor_Tau13A_14LEU-661 ASP-662 ASP-665 ARG-666
4Tau13APO4-2.618receptor_Tau13A_14LEU-661 ASP-662 ASP-665 ARG-666
5Tau13APO4-2.515receptor_Tau13A_15ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 ILE-709THR-703
6Tau13APO4-2.505receptor_Tau13A_1VAL-680 PRO-681 GLY-682 GLY-683 GLY-684 ASN-685 LYS-686 ILE-688
7Tau13APO4-2.498receptor_Tau13A_15ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 ILE-709THR-703
8Tau13APO4-2.963receptor_Tau13A_15ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 ILE-709THR-703
9Tau13APO4-2.593receptor_Tau13A_15ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 ILE-709THR-703