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4ZLY

Crystal Structure of Bruton's Tyrosine Kinase bound to a Cinnoline Fragment

Summary for 4ZLY
Entry DOI10.2210/pdb4zly/pdb
Related4ZLZ
DescriptorTyrosine-protein kinase BTK, IMIDAZOLE, ISOPROPYL ALCOHOL, ... (6 entities in total)
Functional Keywordscytoplasmic tyrosine kinase, transcriptional regulation, nuclear factor-kappab, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (Human)
Cellular locationCytoplasm: Q06187
Total number of polymer chains1
Total formula weight31975.79
Authors
Dougan, D.R. (deposition date: 2015-05-01, release date: 2015-07-01, Last modification date: 2024-03-06)
Primary citationSmith, C.R.,Dougan, D.R.,Komandla, M.,Kanouni, T.,Knight, B.,Lawson, J.D.,Sabat, M.,Taylor, E.R.,Vu, P.,Wyrick, C.
Fragment-Based Discovery of a Small Molecule Inhibitor of Bruton's Tyrosine Kinase.
J.Med.Chem., 58:5437-5444, 2015
Cited by
PubMed Abstract: The discovery and optimization of a series of 4-aminocinnoline-3-carboxamide inhibitors of Bruton's tyrosine kinase are reported. A fragment-based screening approach incorporating X-ray co-crystallography was used to identify a cinnoline fragment and characterize its binding mode in the ATP binding site of Btk. Optimization of the fragment hit resulted in the identification of a lead compound which reduced paw swelling in a dose- and exposure-dependent fashion in a rat model of collagen-induced arthritis.
PubMed: 26087137
DOI: 10.1021/acs.jmedchem.5b00734
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.65 Å)
Structure validation

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数据于2025-06-18公开中

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