Tau3A 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
1Tau3APO4-3.101receptor_Tau3A_10VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau3APO4-2.894receptor_Tau3A_4ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 GLU-708THR-703
3Tau3APO4-2.691receptor_Tau3A_7LYS-664 VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669
4Tau3APO4-2.629receptor_Tau3A_4ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 GLU-708THR-703
5Tau3APO4-2.61receptor_Tau3A_4ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 GLU-708THR-703
6Tau3APO4-2.552receptor_Tau3A_11ASN-727 VAL-728 SER-729 SER-730 THR-731 GLY-732 SER-733 ILE-734SER-729 SER-730 THR-731 SER-733
7Tau3APO4-2.668receptor_Tau3A_11ASN-727 VAL-728 SER-729 SER-730 THR-731 GLY-732 SER-733 ILE-734SER-729 SER-730 THR-731 SER-733
8Tau3APO4-2.69receptor_Tau3A_11ASN-727 VAL-728 SER-729 SER-730 THR-731 GLY-732 SER-733 ILE-734SER-729 SER-730 THR-731 SER-733
9Tau3APO4-2.542receptor_Tau3A_2LEU-693 THR-694 PHE-695 ASN-698THR-694