Tau18E 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
1Tau18EPO4-3.064receptor_Tau18E_10VAL-604 GLN-605 SER-606 CYS-608 GLY-609 LYS-611 ASP-612SER-606
2Tau18EPO4-2.981receptor_Tau18E_12ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 ILE-709THR-703
3Tau18EPO4-2.444receptor_Tau18E_2ASP-270 PHE-271 LEU-272 SER-273 LYS-274SER-273
4Tau18EPO4-2.439receptor_Tau18E_7VAL-573 LYS-574 SER-575 GLY-578 THR-580 GLU-581SER-575 THR-580
5Tau18EPO4-2.394receptor_Tau18E_10VAL-604 GLN-605 SER-606 CYS-608 GLY-609 LYS-611 ASP-612SER-606
6Tau18EPO4-2.387receptor_Tau18E_15ILE-734 ASP-735 MET-736 VAL-737 ASP-738 SER-739 LEU-742SER-739
7Tau18EPO4-2.33receptor_Tau18E_10VAL-604 GLN-605 SER-606 CYS-608 GLY-609 LYS-611 ASP-612SER-606
8Tau18EPO4-2.308receptor_Tau18E_15ILE-734 ASP-735 MET-736 VAL-737 ASP-738 SER-739 LEU-742SER-739
9Tau18EPO4-2.395receptor_Tau18E_15ILE-734 ASP-735 MET-736 VAL-737 ASP-738 SER-739 LEU-742SER-739