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4N70

Pim1 Complexed with a pyridylcarboxamide

Summary for 4N70
Entry DOI10.2210/pdb4n70/pdb
Related4N6Y 4N6Z
DescriptorSerine/threonine-protein kinase pim-1, N-{4-[(3R,4R,5S)-3-amino-4-hydroxy-5-methylpiperidin-1-yl]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide (3 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 weight38054.15
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: 2024-10-30)
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 Abstract: Proviral insertion of Moloney virus (PIM) 1, 2, and 3 kinases are serine/threonine kinases that normally function in survival and proliferation of hematopoietic cells. As high expression of PIM1, 2, and 3 is frequently observed in many human malignancies, including multiple myeloma, non-Hodgkins lymphoma, and myeloid leukemias, there is interest in determining whether selective PIM inhibition can improve outcomes of these human cancers. Herein, we describe our efforts toward this goal. The structure guided optimization of a singleton high throughput screening hit in which the potency against all three PIM isoforms was increased >10,000-fold to yield compounds with pan PIM K is < 10 pM, nanomolar cellular potency, and in vivo activity in an acute myeloid leukemia Pim-dependent tumor model is described.
PubMed: 24900629
DOI: 10.1021/ml400307j
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

238582

數據於2025-07-09公開中

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