Tau8D 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
1Tau8DPO4-2.825receptor_Tau8D_11VAL-573 LYS-574 SER-575 GLY-578 THR-580 GLU-581SER-575 THR-580
2Tau8DPO4-2.74receptor_Tau8D_6VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
3Tau8DPO4-2.565receptor_Tau8D_7ARG-696 GLU-697 ALA-699 SER-726 ASN-727 VAL-728SER-726
4Tau8DPO4-2.596receptor_Tau8D_7ARG-696 GLU-697 ALA-699 SER-726 ASN-727 VAL-728SER-726
5Tau8DPO4-2.555receptor_Tau8D_5LEU-693 THR-694 PHE-695 ASN-698THR-694
6Tau8DPO4-2.513receptor_Tau8D_6VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
7Tau8DPO4-2.503receptor_Tau8D_7ARG-696 GLU-697 ALA-699 SER-726 ASN-727 VAL-728SER-726
8Tau8DPO4-2.472receptor_Tau8D_7ARG-696 GLU-697 ALA-699 SER-726 ASN-727 VAL-728SER-726
9Tau8DPO4-2.719receptor_Tau8D_7ARG-696 GLU-697 ALA-699 SER-726 ASN-727 VAL-728SER-726