Tau20D 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
1Tau20DPO4-2.969receptor_Tau20D_4SER-602 ASN-603 VAL-604 GLN-605 SER-606 LYS-607 CYS-608 GLY-609 LYS-611 ASP-612SER-602 SER-606
2Tau20DPO4-2.893receptor_Tau20D_8LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707THR-703
3Tau20DPO4-2.823receptor_Tau20D_8LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707THR-703
4Tau20DPO4-2.636receptor_Tau20D_19VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
5Tau20DPO4-2.609receptor_Tau20D_8LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707THR-703
6Tau20DPO4-2.537receptor_Tau20D_11ILE-734 ASP-735 MET-736 ASP-738 SER-739 LEU-742SER-739
7Tau20DPO4-2.625receptor_Tau20D_11ILE-734 ASP-735 MET-736 ASP-738 SER-739 LEU-742SER-739
8Tau20DPO4-2.523receptor_Tau20D_15VAL-680 PRO-681 GLY-682 GLY-683 GLY-684 ASN-685
9Tau20DPO4-2.355receptor_Tau20D_18VAL-573 LYS-574 SER-575 GLY-578 THR-580 GLU-581SER-575 THR-580