Tau3B 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
1Tau3BPO4-3.237receptor_Tau3B_7VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau3BPO4-2.81receptor_Tau3B_13LEU-114 GLU-115 ASP-116 GLU-117 ASP-345 THR-346 LYS-347THR-346
3Tau3BPO4-2.815receptor_Tau3B_13LEU-114 GLU-115 ASP-116 GLU-117 ASP-345 THR-346 LYS-347THR-346
4Tau3BPO4-2.676receptor_Tau3B_7VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
5Tau3BPO4-2.659receptor_Tau3B_10LEU-693 THR-694 PHE-695 ASN-698THR-694
6Tau3BPO4-2.61receptor_Tau3B_13LEU-114 GLU-115 ASP-116 GLU-117 ASP-345 THR-346 LYS-347THR-346
7Tau3BPO4-2.556receptor_Tau3B_7VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
8Tau3BPO4-2.558receptor_Tau3B_13LEU-114 GLU-115 ASP-116 GLU-117 ASP-345 THR-346 LYS-347THR-346
9Tau3BPO4-2.546receptor_Tau3B_7VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610