Tau24B 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
1Tau24BPO4-2.824receptor_Tau24B_2VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
2Tau24BPO4-2.822receptor_Tau24B_17LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 ILE-709THR-703
3Tau24BPO4-2.632receptor_Tau24B_17LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 ILE-709THR-703
4Tau24BPO4-2.624receptor_Tau24B_3VAL-604 GLN-605 SER-606 LYS-607 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
5Tau24BPO4-2.507receptor_Tau24B_2VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
6Tau24BPO4-2.561receptor_Tau24B_2VAL-269 ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
7Tau24BPO4-2.504receptor_Tau24B_1LEU-693 THR-694 PHE-695 ASN-698 ALA-699THR-694
8Tau24BPO4-2.489receptor_Tau24B_7PRO-268 VAL-269 ASP-270 PHE-271
9Tau24BPO4-2.436receptor_Tau24B_15VAL-667 GLN-668 SER-669 ILE-671 GLY-672 LEU-674 ASP-675SER-669