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5DA3

Crystal structure of PTK6 Kinase domain with inhibitor

Summary for 5DA3
Entry DOI10.2210/pdb5da3/pdb
DescriptorProtein-tyrosine kinase 6, GLYCEROL, (2-chloro-4-{[6-cyclopropyl-3-(1H-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]amino}phenyl)(morpholin-4-yl)methanone, ... (4 entities in total)
Functional Keywordsptk6, brk, complex, inhibitor, kinase, transferase, imidazo pyrazin, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (Human)
Cellular locationCytoplasm: Q13882
Total number of polymer chains1
Total formula weight31236.44
Authors
Thakur, M.K.,Birudukota, S.,Swaminathan, S.,Battula, S.K.,Vadivelu, S.,Tyagi, R.,Gosu, R. (deposition date: 2015-08-19, release date: 2016-08-24, Last modification date: 2023-11-08)
Primary citationThakur, M.K.,Birudukota, S.,Swaminathan, S.,Battula, S.K.,Vadivelu, S.,Tyagi, R.,Gosu, R.
Co-crystal structures of PTK6: With Dasatinib at 2.24 angstrom , with novel imidazo[1,2-a]pyrazin-8-amine derivative inhibitor at 1.70 angstrom resolution
Biochem. Biophys. Res. Commun., 482:1289-1295, 2017
Cited by
PubMed: 27993680
DOI: 10.1016/j.bbrc.2016.12.030
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.7 Å)
Structure validation

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