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3BEL

X-ray structure of EGFR in complex with oxime inhibitor

Summary for 3BEL
Entry DOI10.2210/pdb3bel/pdb
Related2RGP
DescriptorEpidermal growth factor receptor, PHOSPHATE ION, 4-amino-6-{[1-(3-fluorobenzyl)-1H-indazol-5-yl]amino}pyrimidine-5-carbaldehyde O-(2-methoxyethyl)oxime, ... (4 entities in total)
Functional Keywordskinase domain, alternative splicing, anti-oncogene, atp-binding, cell cycle, disease mutation, glycoprotein, membrane, nucleotide-binding, phosphoprotein, polymorphism, receptor, secreted, transferase, transmembrane, tyrosine-protein kinase, ubl conjugation
Biological sourceHomo sapiens (Human)
Cellular locationCell membrane; Single-pass type I membrane protein. Isoform 2: Secreted: P00533
Total number of polymer chains1
Total formula weight36696.21
Authors
Abad, M.C.,Xu, G.,Neeper, M.P.,Struble, G.T.,Gaul, M.D.,Connolly, P.J. (deposition date: 2007-11-19, release date: 2008-07-01, Last modification date: 2023-08-30)
Primary citationXu, G.,Searle, L.L.,Hughes, T.V.,Beck, A.K.,Connolly, P.J.,Abad, M.C.,Neeper, M.P.,Struble, G.T.,Springer, B.A.,Emanuel, S.L.,Gruninger, R.H.,Pandey, N.,Adams, M.,Moreno-Mazza, S.,Fuentes-Pesquera, A.R.,Middleton, S.A.,Greenberger, L.M.
Discovery of novel 4-amino-6-arylaminopyrimidine-5-carbaldehyde oximes as dual inhibitors of EGFR and ErbB-2 protein tyrosine kinases.
Bioorg.Med.Chem.Lett., 18:3495-3499, 2008
Cited by
PubMed: 18508264
DOI: 10.1016/j.bmcl.2008.05.024
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

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