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3VRZ

Crystal structure of HCK complexed with a pyrrolo-pyrimidine inhibitor 1-[4-(4-amino-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)phenyl]-3-benzylurea

Summary for 3VRZ
Entry DOI10.2210/pdb3vrz/pdb
Related3VRY 3VS0 3VS1 3VS2 3VS3 3VS4 3VS5 3VS6 3VS7
DescriptorTyrosine-protein kinase HCK, CALCIUM ION, CHLORIDE ION, ... (5 entities in total)
Functional Keywordskinase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationIsoform 1: Lysosome. Isoform 2: Cell membrane; Lipid-anchor. Cytoplasmic vesicle, secretory vesicle: P08631
Total number of polymer chains2
Total formula weight105004.54
Authors
Kuratani, M.,Tomabechi, Y.,Handa, N.,Yokoyama, S. (deposition date: 2012-04-21, release date: 2013-05-01, Last modification date: 2023-12-06)
Primary citationSaito, 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: 23596204
DOI: 10.1126/scitranslmed.3004387
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.218 Å)
Structure validation

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