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-Structure paper
Title | Discovery of potent, reversible MetAP2 inhibitors via fragment based drug discovery and structure based drug design-Part 1. |
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Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 26, Page 2774-2778, Year 2016 |
Publish date | Apr 21, 2016 (structure data deposition date) |
![]() | Cheruvallath, Z. / Tang, M. / McBride, C. / Komandla, M. / Miura, J. / Ton-Nu, T. / Erikson, P. / Feng, J. / Farrell, P. / Lawson, J.D. ...Cheruvallath, Z. / Tang, M. / McBride, C. / Komandla, M. / Miura, J. / Ton-Nu, T. / Erikson, P. / Feng, J. / Farrell, P. / Lawson, J.D. / Vanderpool, D. / Wu, Y. / Dougan, D.R. / Plonowski, A. / Holub, C. / Larson, C. |
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Methods | X-ray diffraction |
Resolution | 1.8 - 2.15 Å |
Structure data | ![]() PDB-5jhu: ![]() PDB-5ji6: |
Chemicals | ![]() ChemComp-MN: ![]() ChemComp-GOL: ![]() ChemComp-DMS: ![]() ChemComp-6KO: ![]() ChemComp-HOH: ![]() ChemComp-SO4: ![]() ChemComp-6KN: |
Source |
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![]() | Hydrolase/Hydrolase Inhibitor / Hydrolase / peptidase / metal ion binding / proteolysis / Hydrolase-Hydrolase Inhibitor complex / Hydrolase4/Hydrolase Inhibitor / Hydrolase4-Hydrolase Inhibitor complex |