4BB4
ephB4 kinase domain inhibitor complex
Summary for 4BB4
Entry DOI | 10.2210/pdb4bb4/pdb |
Related | 2BBA 2VWU 2VWV 2VWW 2VWX 2VWY 2VWZ 2VX0 2VX1 2X9F 2XVD 4AW5 |
Descriptor | EPHRIN TYPE-B RECEPTOR 4, N-(2-methoxyethyl)-4-[(6-pyridin-4-ylquinazolin-2-yl)amino]benzamide, MAGNESIUM ION, ... (4 entities in total) |
Functional Keywords | transferase, unphosphorylated |
Biological source | HOMO SAPIENS (HUMAN) |
Total number of polymer chains | 1 |
Total formula weight | 34382.87 |
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: 2024-05-08) |
Primary citation | Vasbinder, 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: 23398453DOI: 10.1021/JM301658D PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.65 Å) |
Structure validation
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