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-Structure paper
Title | Structure-based design, synthesis, and memapsin 2 (BACE) inhibitory activity of carbocyclic and heterocyclic peptidomimetics |
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Journal, issue, pages | J. Med. Chem., Vol. 48, Page 5175-5190, Year 2005 |
Publish date | Jan 20, 2005 (structure data deposition date) |
Authors | Hanessian, S. / Yun, H. / Hou, Y. / Yang, G. / Bayrakdarian, M. / Therrien, E. / Moitessier, N. / Roggo, S. / Veenstra, S. / Tintelnot-Blomley, M. ...Hanessian, S. / Yun, H. / Hou, Y. / Yang, G. / Bayrakdarian, M. / Therrien, E. / Moitessier, N. / Roggo, S. / Veenstra, S. / Tintelnot-Blomley, M. / Rondeau, J.M. / Ostermeier, C. / Strauss, A. / Ramage, P. / Paganetti, P. / Neumann, U. / Betschart, C. |
External links | J. Med. Chem. / PubMed:16078837 |
Methods | X-ray diffraction |
Resolution | 2.05 - 2.25 Å |
Structure data | PDB-1ym2: PDB-1ym4: |
Chemicals | ChemComp-HOH: |
Source |
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Keywords | HYDROLASE/HYDROLASE INHIBITOR / BETA-SECRETASE / MEMAPSIN2 / ALZHEIMER'S DISEASE / ASPARTIC PROTEASE / HYDROLASE / HYDROLASE-HYDROLASE INHIBITOR complex |