8BIN
Crystal structure of human Ephrin type-A receptor 2 (EPHA2) Kinase domain in complex with MR21
Summary for 8BIN
Entry DOI | 10.2210/pdb8bin/pdb |
Descriptor | Ephrin type-A receptor 2, 1,2-ETHANEDIOL, 8-(4-azanylbutyl)-6-(2-chlorophenyl)-2-(methylamino)pyrido[2,3-d]pyrimidin-7-one, ... (4 entities in total) |
Functional Keywords | epha2, eck, typ i inhibitor, transferase |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 35255.15 |
Authors | Zhubi, R.,Rak, M.,Knapp, S.,Kraemer, A.,Structural Genomics Consortium (SGC) (deposition date: 2022-11-02, release date: 2022-11-23, Last modification date: 2024-07-31) |
Primary citation | Gerninghaus, J.,Zhubi, R.,Kramer, A.,Karim, M.,Tran, D.H.N.,Joerger, A.C.,Schreiber, C.,Berger, L.M.,Berger, B.T.,Ehret, T.A.L.,Elson, L.,Lenz, C.,Saxena, K.,Muller, S.,Einav, S.,Knapp, S.,Hanke, T. Back-Pocket Optimization of 2-Aminopyrimidine-Based Macrocycles Leads to Potent EPHA2/GAK Kinase Inhibitors. J.Med.Chem., 2024 Cited by PubMed: 39028937DOI: 10.1021/acs.jmedchem.4c00411 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.5 Å) |
Structure validation
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