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9YKO

Crystal structure of human DYRK1A kinase bound with inhibitor FC3

This is a non-PDB format compatible entry.
Summary for 9YKO
Entry DOI10.2210/pdb9yko/pdb
DescriptorDual specificity tyrosine-phosphorylation-regulated kinase 1A, (5,6-dihydroxy-1,3-benzothiazol-2-yl)(3,4-dihydroxyphenyl)methanone (3 entities in total)
Functional Keywordskinase, inhibitor, co-crystallization, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains4
Total formula weight168666.21
Authors
Elkayam, E.,Garg, A.,Joshua-Tor, L. (deposition date: 2025-10-07, release date: 2026-06-17)
Primary citationVenkataramani, P.,Elkayam, E.,Garg, A.,Cheng, K.F.,Altiti, A.,He, M.,Thakur, K.,Michalopoulou, E.,Gonzalez, C.,Felice, C.,Van Aelst, L.,Pappin, D.,Joshua-Tor, L.,Al-Abed, Y.,Tonks, N.K.
Small-molecule inhibitors of the protein kinase DYRK as potential therapeutic candidates in cancer
Cell Chem Biol, 2026
Cited by
DOI: 10.1016/j.chembiol.2026.05.005
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.77 Å)
Structure validation

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PDB entries from 2026-06-17

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