Tau18B 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
1Tau18BPO4-3.159receptor_Tau18B_2VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau18BPO4-2.646receptor_Tau18B_2VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
3Tau18BPO4-2.714receptor_Tau18B_2VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
4Tau18BPO4-2.672receptor_Tau18B_2VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
5Tau18BPO4-2.562receptor_Tau18B_11LYS-660 LEU-661 ASP-662 PHE-663 ASP-665 ARG-666 VAL-667
6Tau18BPO4-2.385receptor_Tau18B_8LEU-693 THR-694 PHE-695 ASN-698THR-694
7Tau18BPO4-2.317receptor_Tau18B_11LYS-660 LEU-661 ASP-662 PHE-663 ASP-665 ARG-666 VAL-667
8Tau18BPO4-2.307receptor_Tau18B_2VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
9Tau18BPO4-2.245receptor_Tau18B_13PRO-587 GLY-588 GLY-589 GLY-590 LYS-591