4X0M
Selection of fragments for kinase inhibitor design: decoration is key
Summary for 4X0M
Entry DOI | 10.2210/pdb4x0m/pdb |
Related | 1vjy |
Descriptor | TGF-beta receptor type-1, 4-aminopyrido[2,3-d]pyrimidin-5(8H)-one, SULFATE ION, ... (4 entities in total) |
Functional Keywords | transferase, protein kinase, inhibitor complex |
Biological source | Homo sapiens (Human) |
Cellular location | Cell membrane; Single-pass type I membrane protein: P36897 |
Total number of polymer chains | 1 |
Total formula weight | 35140.36 |
Authors | Czodrowski, P.,Hoelzemann, G.,Barnickel, G.,Greiner, H.,Musil, D. (deposition date: 2014-11-21, release date: 2014-12-24, Last modification date: 2024-01-10) |
Primary citation | Czodrowski, P.,Holzemann, G.,Barnickel, G.,Greiner, H.,Musil, D. Selection of fragments for kinase inhibitor design: decoration is key. J.Med.Chem., 58:457-465, 2015 Cited by PubMed: 25437144DOI: 10.1021/jm501597j PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.68 Å) |
Structure validation
Download full validation report