Tau17D 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
1Tau17DPO4-3.207receptor_Tau17D_4VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
2Tau17DPO4-2.691receptor_Tau17D_5LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 ILE-709THR-703
3Tau17DPO4-2.628receptor_Tau17D_5LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 ILE-709THR-703
4Tau17DPO4-2.543receptor_Tau17D_5LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 ILE-709THR-703
5Tau17DPO4-2.727receptor_Tau17D_5LYS-700 ALA-701 THR-703 ASP-704 HIS-705 GLY-706 ALA-707 ILE-709THR-703
6Tau17DPO4-2.504receptor_Tau17D_4VAL-604 GLN-605 SER-606 CYS-608 GLY-609 SER-610 LYS-611 ASP-612SER-606 SER-610
7Tau17DPO4-2.449receptor_Tau17D_11VAL-573 LYS-574 SER-575 GLY-578 THR-580 GLU-581SER-575 THR-580
8Tau17DPO4-2.574receptor_Tau17D_11VAL-573 LYS-574 SER-575 GLY-578 THR-580 GLU-581SER-575 THR-580
9Tau17DPO4-2.372receptor_Tau17D_8VAL-680 PRO-681 GLY-682 GLY-683 GLY-684 ASN-685