Tau4B 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
1Tau4BPO4-2.843receptor_Tau4B_3VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau4BPO4-2.816receptor_Tau4B_12ASP-270 PHE-271 LEU-272 SER-273 LYS-274 VAL-275SER-273
3Tau4BPO4-2.415receptor_Tau4B_12ASP-270 PHE-271 LEU-272 SER-273 LYS-274 VAL-275SER-273
4Tau4BPO4-2.481receptor_Tau4B_12ASP-270 PHE-271 LEU-272 SER-273 LYS-274 VAL-275SER-273
5Tau4BPO4-2.409receptor_Tau4B_12ASP-270 PHE-271 LEU-272 SER-273 LYS-274 VAL-275SER-273
6Tau4BPO4-2.377receptor_Tau4B_12ASP-270 PHE-271 LEU-272 SER-273 LYS-274 VAL-275SER-273
7Tau4BPO4-2.363receptor_Tau4B_12ASP-270 PHE-271 LEU-272 SER-273 LYS-274 VAL-275SER-273
8Tau4BPO4-2.315receptor_Tau4B_9LYS-692 LEU-693 THR-694 PHE-695 ASN-698 ALA-699THR-694
9Tau4BPO4-2.295receptor_Tau4B_16ASP-13 HIS-14 ALA-15 GLY-16 THR-17THR-17