4WA9
The crystal structure of human abl1 wild type kinase domain in complex with axitinib
Summary for 4WA9
Entry DOI | 10.2210/pdb4wa9/pdb |
Descriptor | Tyrosine-protein kinase ABL1, AXITINIB (3 entities in total) |
Functional Keywords | kinase, kinase inhibitor, axitinib, activation loop, dfg-out, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Homo sapiens (Human) |
Cellular location | Cytoplasm, cytoskeleton. Isoform IB: Nucleus membrane; Lipid-anchor: P00519 |
Total number of polymer chains | 2 |
Total formula weight | 66854.39 |
Authors | Johnson, E.,McTigue, M.,Cronin, C.N. (deposition date: 2014-08-28, release date: 2015-02-11, Last modification date: 2024-08-07) |
Primary citation | Pemovska, T.,Johnson, E.,Kontro, M.,Repasky, G.A.,Chen, J.,Wells, P.,Cronin, C.N.,McTigue, M.,Kallioniemi, O.,Porkka, K.,Murray, B.W.,Wennerberg, K. Axitinib effectively inhibits BCR-ABL1(T315I) with a distinct binding conformation. Nature, 519:102-105, 2015 Cited by PubMed: 25686603DOI: 10.1038/nature14119 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.2 Å) |
Structure validation
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