4CR9
Creating novel F1 inhibitors through fragment based lead generation and structure aided drug design
Summary for 4CR9
Entry DOI | 10.2210/pdb4cr9/pdb |
Related | 4CR5 4CRA 4CRB 4CRC 4CRD 4CRE 4CRF 4CRG |
Descriptor | COAGULATION FACTOR XI, 4-methylquinoline-2,6-diamine, SULFATE ION, ... (4 entities in total) |
Functional Keywords | hydrolase |
Biological source | HOMO SAPIENS (HUMAN) |
Cellular location | Secreted: P03951 |
Total number of polymer chains | 1 |
Total formula weight | 27501.96 |
Authors | Sandmark, J.,Oster, L.,Fjellstrom, O.,Akkaya, S.,Beisel, H.G.,Eriksson, P.O.,Erixon, K.,Gustafsson, D.,Jurva, U.,Kang, D.,Karis, D.,Knecht, W.,Nerme, V.,Nilsson, I.,Olsson, T.,Redzic, A.,Roth, R.,Tigerstrom, A. (deposition date: 2014-02-26, release date: 2015-02-11, Last modification date: 2018-04-04) |
Primary citation | Fjellstrom, O.,Akkaya, S.,Beisel, H.,Eriksson, P.,Erixon, K.,Gustafsson, D.,Jurva, U.,Kang, D.,Karis, D.,Knecht, W.,Nerme, V.,Nilsson, I.,Olsson, T.,Redzic, A.,Roth, R.,Sandmark, J.,Tigerstrom, A.,Oster, L. Creating Novel Activated Factor Xi Inhibitors Through Fragment Based Lead Generation and Structure Aided Drug Design. Plos One, 10:13705-, 2015 Cited by PubMed: 25629509DOI: 10.1371/JOURNAL.PONE.0113705 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.7 Å) |
Structure validation
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