5FXS
IGFR-1R complex with a pyrimidine inhibitor.
Summary for 5FXS
Entry DOI | 10.2210/pdb5fxs/pdb |
Related | 5FXQ 5FXR |
Descriptor | INSULIN-LIKE GROWTH FACTOR 1 RECEPTOR, ACETATE ION, 2-[4-[4-[[(6Z)-5-chloranyl-6-pyrazolo[1,5-a]pyridin-3-ylidene-1H-pyrimidin-2-yl]amino]-3,5-dimethyl-pyrazol-1-yl]piperidin-1-yl]-N,N-dimethyl-ethanamide, ... (4 entities in total) |
Functional Keywords | transferase |
Biological source | HOMO SAPIENS (HUMAN) |
Total number of polymer chains | 1 |
Total formula weight | 35851.46 |
Authors | Degorce, S.,Boyd, S.,Curwen, J.,Ducray, R.,Halsall, C.,Jones, C.,Lach, F.,Lenz, E.,Pass, M.,Pass, S.,Trigwell, C.,Norman, R.,Phillips, C. (deposition date: 2016-03-02, release date: 2016-10-19, Last modification date: 2018-07-11) |
Primary citation | Degorce, S.L.,Boyd, S.,Curwen, J.O.,Ducray, R.,Halsall, C.T.,Jones, C.D.,Lach, F.,Lenz, E.M.,Pass, M.,Pass, S.,Trigwell, C. Discovery of a Potent, Selective, Orally Bioavailable, and Efficacious Novel 2-(Pyrazol-4-ylamino)-pyrimidine Inhibitor of the Insulin-like Growth Factor-1 Receptor (IGF-1R). J. Med. Chem., 59:4859-4866, 2016 Cited by PubMed: 27078757DOI: 10.1021/acs.jmedchem.6b00203 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.9 Å) |
Structure validation
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