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-Structure paper
Title | Fused-ring structure of decahydroisoquinolin as a novel scaffold for SARS 3CL protease inhibitors |
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Journal, issue, pages | Bioorg. Med. Chem., Vol. 23, Page 876-890, Year 2015 |
Publish date | Jul 2, 2014 (structure data deposition date) |
Authors | Shimamoto, Y. / Hattori, Y. / Kobayashi, K. / Teruya, K. / Sanjoh, A. / Nakagawa, A. / Yamashita, E. / Akaji, K. |
External links | Bioorg. Med. Chem. / PubMed:25614110 |
Methods | X-ray diffraction |
Resolution | 1.6 - 2.42 Å |
Structure data | PDB-4tww: PDB-4twy: PDB-4wy3: |
Chemicals | ChemComp-3A7: ChemComp-HOH: ChemComp-3BL: ChemComp-3X5: |
Source |
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Keywords | HYDROLASE/HYDROLASE INHIBITOR / hydrase proteinase converting / designed inhibitor / hydrase-inhibitor complex / HYDROLASE-HYDROLASE INHIBITOR complex |