Tau1B 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
1Tau1BPO4-3.113receptor_Tau1B_7VAL-604 GLN-605 SER-606 CYS-608 GLY-609 LYS-611 ASP-612SER-606
2Tau1BPO4-2.935receptor_Tau1B_12VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
3Tau1BPO4-2.653receptor_Tau1B_4LYS-692 LEU-693 THR-694 PHE-695 ASN-698THR-694
4Tau1BPO4-2.536receptor_Tau1B_11VAL-728 SER-729 SER-730 THR-731 GLY-732 ILE-734SER-729 SER-730 THR-731
5Tau1BPO4-2.463receptor_Tau1B_12VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
6Tau1BPO4-2.681receptor_Tau1B_12VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
7Tau1BPO4-2.502receptor_Tau1B_12VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
8Tau1BPO4-2.699receptor_Tau1B_12VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
9Tau1BPO4-2.428receptor_Tau1B_10LYS-692 LEU-693 THR-694 PHE-695 ARG-696 GLU-697THR-694