3VS0
Crystal structure of HCK complexed with a pyrrolo-pyrimidine inhibitor N-[4-(4-amino-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)phenyl]benzamide
Summary for 3VS0
Entry DOI | 10.2210/pdb3vs0/pdb |
Related | 3VRY 3VRZ 3VS1 3VS2 3VS3 3VS4 3VS5 3VS6 3VS7 |
Descriptor | Tyrosine-protein kinase HCK, CALCIUM ION, CHLORIDE ION, ... (5 entities in total) |
Functional Keywords | kinase, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Isoform 1: Lysosome. Isoform 2: Cell membrane; Lipid-anchor. Cytoplasmic vesicle, secretory vesicle: P08631 |
Total number of polymer chains | 2 |
Total formula weight | 104946.46 |
Authors | Kuratani, M.,Honda, K.,Tomabechi, Y.,Handa, N.,Yokoyama, S. (deposition date: 2012-04-21, release date: 2013-05-01, Last modification date: 2023-12-06) |
Primary citation | Saito, Y.,Yuki, H.,Kuratani, M.,Hashizume, Y.,Takagi, S.,Honma, T.,Tanaka, A.,Shirouzu, M.,Mikuni, J.,Handa, N.,Ogahara, I.,Sone, A.,Najima, Y.,Tomabechi, Y.,Wakiyama, M.,Uchida, N.,Tomizawa-Murasawa, M.,Kaneko, A.,Tanaka, S.,Suzuki, N.,Kajita, H.,Aoki, Y.,Ohara, O.,Shultz, L.D.,Fukami, T.,Goto, T.,Taniguchi, S.,Yokoyama, S.,Ishikawa, F. A Pyrrolo-Pyrimidine Derivative Targets Human Primary AML Stem Cells in Vivo Sci Transl Med, 5:181ra52-181ra52, 2013 Cited by PubMed: 23596204DOI: 10.1126/scitranslmed.3004387 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.934 Å) |
Structure validation
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