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| Title | Potent antiviral HIV-1 protease inhibitor GRL-02031 adapts to the structures of drug resistant mutants with its P1'-pyrrolidinone ring. |
|---|---|
| Journal, issue, pages | J. Med. Chem., Vol. 55, Page 3387-3397, Year 2012 |
| Publish date | Jan 9, 2012 (structure data deposition date) |
Authors | Chang, Y.C. / Yu, X. / Zhang, Y. / Tie, Y. / Wang, Y.F. / Yashchuk, S. / Ghosh, A.K. / Harrison, R.W. / Weber, I.T. |
External links | J. Med. Chem. / PubMed:22401672 |
| Methods | X-ray diffraction |
| Resolution | 1.25 - 1.55 Å |
| Structure data | ![]() PDB-3vf5: ![]() PDB-3vf7: ![]() PDB-3vfa: ![]() PDB-3vfb: |
| Chemicals | ![]() ChemComp-NA: ![]() ChemComp-CL: ![]() ChemComp-ACT: ![]() ChemComp-031: ![]() ChemComp-GOL: ![]() ChemComp-HOH: |
| Source |
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Keywords | hydrolase/hydrolase inhibitor / protease inhibitor / P1'-ligand / hydrolase-hydrolase inhibitor complex |
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human immunodeficiency virus type 1 (bru isolate)
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