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9D4W

Structure of PAK1 in complex with compound 12

This is a non-PDB format compatible entry.
Summary for 9D4W
Entry DOI10.2210/pdb9d4w/pdb
DescriptorSerine/threonine-protein kinase PAK 1, N~2~-{[(1s,4s)-4-aminocyclohexyl]methyl}-N~4~-[5-(trifluoromethyl)-1,3-thiazol-2-yl]pyrimidine-2,4-diamine (3 entities in total)
Functional Keywordsserine/threonine-protein kinase, transferase, inhibitor
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight67317.36
Authors
Dementiev, A.,Suto, R.K.,Olland, A.M. (deposition date: 2024-08-13, release date: 2025-04-02)
Primary citationJohns, D.,Olejniczak, J.,Babbar, A.,Boone, C.,Cakici, O.,Cheng, M.,Cheng, Q.,Dementiev, A.,Eick, M.,Ferdyan, N.,Fontano, E.,Forman, A.,Goel, V.,Hirst, G.,Kozlowski, R.,Lee, S.,Mehta, S.,Mowery, K.,Murray, B.,Nguyen, V.,Olland, A.,Phan, K.,Reich, S.,Rivera, L.,Sabat, M.,Sprengeler, P.,Srinivasan, K.,Sun, Z.,Suto, R.,Wilkinson, T.,Wang, C.,Yu, N.,Xu, M.
Identification of a p21-Activated Kinase 1 (PAK1) Inhibitor with 10-fold Selectivity Against PAK2
To Be Published,
Experimental method
X-RAY DIFFRACTION (2.218 Å)
Structure validation

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