9FUF
Crystal structure of human DYRK1A in complex with ARN25641
This is a non-PDB format compatible entry.
Summary for 9FUF
| Entry DOI | 10.2210/pdb9fuf/pdb |
| Related | 9FR5 9FR6 9FR7 9FR8 9FR9 |
| Descriptor | Dual specificity tyrosine-phosphorylation-regulated kinase 1A, 3-[[[4-[(3-cyclopropyl-1~{H}-pyrazol-5-yl)amino]thieno[3,2-d]pyrimidin-2-yl]amino]methyl]benzamide (3 entities in total) |
| Functional Keywords | kinase inhibitors, multitarget compounds, drug discovery, central nervous system, tauopathies, transferase |
| Biological source | Homo sapiens (human) |
| Total number of polymer chains | 1 |
| Total formula weight | 42422.90 |
| Authors | Dalle Vedove, A.,Demuro, S.,Di Martino, R.M.C.,Balboni, B.,Tripathi, S.K.,Storici, P.,Girotto, S.,Cavalli, A. (deposition date: 2024-06-26, release date: 2026-01-14) |
| Primary citation | Demuro, S. Unveiling the pharmacophoric traits of balanced triple GSK-3B/FYN/DYRK1A inhibitors: rational design and synthesis of novel amino-pyrazole containing scaffolds for the treatment of Alzheimer's disease and related tauopathies. To Be Published, |
| Experimental method | X-RAY DIFFRACTION (2.7 Å) |
Structure validation
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