PDB ID: 4CR5
Hetero Atom Contents
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Structure summary
| Code : | 4CR5 PDBj RCSB PDB PDBe | ||||||||||||
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| Header : | HYDROLASE | ||||||||||||
| Title : | Creating novel F1 inhibitors through fragment based lead generation and structure aided drug design | ||||||||||||
| Release Data : | 2015-02-11 | ||||||||||||
| Compound : |
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| Source : |
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| 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. | ||||||||||||
| Keywords : | HYDROLASE | ||||||||||||
| Exp. method : | X-RAY DIFFRACTION ( 2.00 Å ) | ||||||||||||
| Citation : |
Creating Novel Activated Factor Xi Inhibitors Through Fragment Based Lead Generation and Structure Aided Drug Design.
Fjellstrom, O.,Akkaya, S.,Beisel, H.
et al.
PubMed: 25629509 |
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Reaction
| Chain : | A | ||||||||
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| UniProt : | P03951 (FA11_HUMAN) | ||||||||
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