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2VX1

ephB4 kinase domain inhibitor complex

Summary for 2VX1
Entry DOI10.2210/pdb2vx1/pdb
Related2BBA 2VWU 2VWV 2VWW 2VWX 2VWY 2VWZ 2VX0
DescriptorEPHRIN TYPE-B RECEPTOR 4, 3-({4-[(5-CHLORO-1,3-BENZODIOXOL-4-YL)AMINO]PYRIMIDIN-2-YL}AMINO)BENZAMIDE, MAGNESIUM ION, ... (4 entities in total)
Functional Keywordstyrosine-protein kinase, receptor tyrosine kinase, kinase, mutant, membrane, receptor, transferase, atp-binding, polymorphism, glycoprotein, transmembrane, phosphoprotein, unphosphorylated, nucleotide-binding
Biological sourceHOMO SAPIENS (HUMAN)
Total number of polymer chains1
Total formula weight34391.52
Authors
Read, J.,Brassington, C.A.,Green, I.,McCall, E.J.,Valentine, A.L.,Barratt, D.,Leach, A.G.,Kettle, J.G. (deposition date: 2008-06-30, release date: 2008-10-28, Last modification date: 2023-12-13)
Primary citationBardelle, C.,Coleman, T.,Cross, D.,Davenport, S.,Kettle, J.G.,Ko, E.J.,Leach, A.G.,Mortlock, A.,Read, J.,Roberts, N.J.,Robins, P.,Williams, E.J.
Inhibitors of the Tyrosine Kinase Ephb4. Part 2: Structure-Based Discovery and Optimisation of 3,5-Bis Substituted Anilinopyrimidines.
Bioorg.Med.Chem.Lett., 18:5717-, 2008
Cited by
PubMed: 18851911
DOI: 10.1016/J.BMCL.2008.09.087
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.65 Å)
Structure validation

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