+Search query
-Structure paper
| Title | Design of HIV-1 protease inhibitors with pyrrolidinones and oxazolidinones as novel P1'-ligands to enhance backbone-binding interactions with protease: synthesis, biological evaluation, and protein-ligand X-ray studies. |
|---|---|
| Journal, issue, pages | J. Med. Chem., Vol. 52, Page 3902-3914, Year 2009 |
| Publish date | Apr 21, 2009 (structure data deposition date) |
Authors | Ghosh, A.K. / Leshchenko-Yashchuk, S. / Anderson, D.D. / Baldridge, A. / Noetzel, M. / Miller, H.B. / Tie, Y. / Wang, Y.F. / Koh, Y. / Weber, I.T. / Mitsuya, H. |
External links | J. Med. Chem. / PubMed:19473017 |
| Methods | X-ray diffraction |
| Resolution | 1.29 Å |
| Structure data | ![]() PDB-3h5b: |
| Chemicals | ![]() ChemComp-NA: ![]() ChemComp-CL: ![]() ChemComp-031: ![]() ChemComp-GOL: ![]() ChemComp-HOH: |
| Source |
|
Keywords | HYDROLASE / HIV-1 / wild type protease / protease inhibitor / P1'-ligand / AIDS |
Movie
Controller
Structure viewers
About Yorodumi Papers



Authors
External links





human immunodeficiency virus type 1 (bru isolate)
Keywords