3NUX
CDK6 (monomeric) in complex with inhibitor
Summary for 3NUX
Entry DOI | 10.2210/pdb3nux/pdb |
Related | 3NUP |
Descriptor | Cell division protein kinase 6, 4-[5-chloro-3-(1-methylethyl)-1H-pyrazol-4-yl]-N-(5-piperazin-1-ylpyridin-2-yl)pyrimidin-2-amine (3 entities in total) |
Functional Keywords | kinase, protein kinase, atp binding, phosphorylation, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Cytoplasm: Q00534 |
Total number of polymer chains | 1 |
Total formula weight | 35418.11 |
Authors | Chopra, R. (deposition date: 2010-07-07, release date: 2010-12-22, Last modification date: 2024-02-21) |
Primary citation | Cho, Y.S.,Borland, M.,Brain, C.,Chen, C.H.,Cheng, H.,Chopra, R.,Chung, K.,Groarke, J.,He, G.,Hou, Y.,Kim, S.,Kovats, S.,Lu, Y.,O'Reilly, M.,Shen, J.,Smith, T.,Trakshel, G.,Vogtle, M.,Xu, M.,Xu, M.,Sung, M.J. 4-(Pyrazol-4-yl)-pyrimidines as selective inhibitors of cyclin-dependent kinase 4/6. J.Med.Chem., 53:7938-7957, 2010 Cited by PubMed: 21038853DOI: 10.1021/jm100571n PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.7 Å) |
Structure validation
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