3FZ1
Crystal structure of a benzthiophene inhibitor bound to human Cyclin-dependent Kinase-2 (CDK-2)
Summary for 3FZ1
Entry DOI | 10.2210/pdb3fz1/pdb |
Related | 1AQ1 3FYK |
Descriptor | Cell division protein kinase 2, (3R)-3-(aminomethyl)-9-methoxy-1,2,3,4-tetrahydro-5H-[1]benzothieno[3,2-e][1,4]diazepin-5-one (3 entities in total) |
Functional Keywords | cdk-2, mk-2, mk2, mapkap kinase-2, ser/thr kinase, cell divison kinase-2, cyclin, benzothiophene, atp-binding, cell cycle, cell division, kinase, mitosis, nucleotide-binding, phosphoprotein, polymorphism, serine/threonine-protein kinase, transferase |
Biological source | Homo sapiens (human) |
Cellular location | Cytoplasm, cytoskeleton, microtubule organizing center, centrosome: P24941 |
Total number of polymer chains | 1 |
Total formula weight | 34253.83 |
Authors | Kurumbail, R.G.,Caspers, N. (deposition date: 2009-01-23, release date: 2009-04-07, Last modification date: 2023-09-06) |
Primary citation | Anderson, D.R.,Meyers, M.J.,Kurumbail, R.G.,Caspers, N.,Poda, G.I.,Long, S.A.,Pierce, B.S.,Mahoney, M.W.,Mourey, R.J.,Parikh, M.D. Benzothiophene inhibitors of MK2. Part 2: improvements in kinase selectivity and cell potency. Bioorg.Med.Chem.Lett., 19:4882-4884, 2009 Cited by PubMed: 19616942DOI: 10.1016/j.bmcl.2009.02.017 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.9 Å) |
Structure validation
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