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-Structure paper
| Title | Synthesis of new (-)-bestatin-based inhibitor libraries reveals a novel binding mode in the s1 pocket of the essential malaria m1 metalloaminopeptidase. |
|---|---|
| Journal, issue, pages | J. Med. Chem., Vol. 54, Page 1655-1666, Year 2011 |
| Publish date | Dec 22, 2010 (structure data deposition date) |
Authors | Velmourougane, G. / Harbut, M.B. / Dalal, S. / McGowan, S. / Oellig, C.A. / Meinhardt, N. / Whisstock, J.C. / Klemba, M. / Greenbaum, D.C. |
External links | J. Med. Chem. / PubMed:21366301 |
| Methods | X-ray diffraction |
| Resolution | 1.8 Å |
| Structure data | ![]() PDB-3q43: ![]() PDB-3q44: |
| Chemicals | ![]() ChemComp-ZN: ![]() ChemComp-MG: ![]() ChemComp-GOL: ![]() ChemComp-D66: ![]() ChemComp-HOH: ![]() ChemComp-D50: |
| Source |
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Keywords | HYDROLASE/HYDROLASE INHIBITOR / M1 Aminopeptidase / HYDROLASE-HYDROLASE INHIBITOR complex |
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