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3PA3

X-ray crystal structure of compound 70 bound to human CHK1 kinase domain

Summary for 3PA3
Entry DOI10.2210/pdb3pa3/pdb
DescriptorSerine/threonine-protein kinase Chk1, 2-(4-chlorophenyl)-4-[(3S)-piperidin-3-ylamino]thieno[2,3-d]pyridazine-7-carboxamide (3 entities in total)
Functional Keywordskinase, phosphatase, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationNucleus: O14757
Total number of polymer chains1
Total formula weight31843.12
Authors
Fischmann, T.O. (deposition date: 2010-10-18, release date: 2010-12-08, Last modification date: 2024-02-21)
Primary citationZhao, L.,Zhang, Y.,Dai, C.,Guzi, T.,Wiswell, D.,Seghezzi, W.,Parry, D.,Fischmann, T.,Siddiqui, M.A.
Design, synthesis and SAR of thienopyridines as potent CHK1 inhibitors.
Bioorg.Med.Chem.Lett., 20:7216-7221, 2010
Cited by
PubMed: 21074424
DOI: 10.1016/j.bmcl.2010.10.105
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.4 Å)
Structure validation

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