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4N6Z

Pim1 Complexed with a pyridylcarboxamide

Summary for 4N6Z
Entry DOI10.2210/pdb4n6z/pdb
Related4N6Y 4N70
DescriptorSerine/threonine-protein kinase pim-1, 3-amino-N-{4-[(3S)-3-aminopiperidin-1-yl]pyridin-3-yl}pyrazine-2-carboxamide, GLYCEROL, ... (4 entities in total)
Functional Keywordskinase, phosphorylation, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationIsoform 2: Cytoplasm. Isoform 1: Cell membrane: P11309
Total number of polymer chains1
Total formula weight38186.34
Authors
Bellamacina, C.R.,Le, V.,Shu, W.,Burger, M.T.,Bussiere, D. (deposition date: 2013-10-14, release date: 2013-11-06, Last modification date: 2014-07-02)
Primary citationBurger, M.T.,Han, W.,Lan, J.,Nishiguchi, G.,Bellamacina, C.,Lindval, M.,Atallah, G.,Ding, Y.,Mathur, M.,McBride, C.,Beans, E.L.,Muller, K.,Tamez, V.,Zhang, Y.,Huh, K.,Feucht, P.,Zavorotinskaya, T.,Dai, Y.,Holash, J.,Castillo, J.,Langowski, J.,Wang, Y.,Chen, M.Y.,Garcia, P.D.
Structure Guided Optimization, in Vitro Activity, and in Vivo Activity of Pan-PIM Kinase Inhibitors.
ACS Med Chem Lett, 4:1193-1197, 2013
Cited by
PubMed: 24900629
DOI: 10.1021/ml400307j
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

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