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4BB4

ephB4 kinase domain inhibitor complex

Summary for 4BB4
Entry DOI10.2210/pdb4bb4/pdb
Related2BBA 2VWU 2VWV 2VWW 2VWX 2VWY 2VWZ 2VX0 2VX1 2X9F 2XVD 4AW5
DescriptorEPHRIN TYPE-B RECEPTOR 4, N-(2-methoxyethyl)-4-[(6-pyridin-4-ylquinazolin-2-yl)amino]benzamide, MAGNESIUM ION, ... (4 entities in total)
Functional Keywordstransferase, unphosphorylated
Biological sourceHOMO SAPIENS (HUMAN)
Total number of polymer chains1
Total formula weight34382.87
Authors
Read, J.,Brassington, C.A.,Green, I.,McCall, E.J.,Valentine, A.L. (deposition date: 2012-09-19, release date: 2013-02-27, Last modification date: 2019-04-24)
Primary citationVasbinder, M.M.,Aquila, B.,Augustin, M.,Chen, H.,Cheung, T.,Cook, D.,Drew, L.,Fauber, B.P.,Glossop, S.,Grondine, M.,Hennessy, E.J.,Johannes, J.,Lee, S.,Lyne, P.D.,Mortl, M.,Omer, C.,Palakurthi, S.,Pontz, T.,Read, J.,Sha, L.,Shen, M.,Steinbacher, S.,Wang, H.,Wu, A.,Ye, M.
Discovery and Optimization of a Novel Series of Potent Mutant B-Raf V600E Selective Kinase Inhibitors.
J.Med.Chem., 56:1996-, 2013
Cited by
PubMed: 23398453
DOI: 10.1021/JM301658D
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.65 Å)
Structure validation

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