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-Structure paper
Title | Structure-based design and synthesis of non-nucleoside, potent, and orally bioavailable adenosine deaminase inhibitors |
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Journal, issue, pages | J. Med. Chem., Vol. 47, Page 2728-2731, Year 2004 |
Publish date | Dec 14, 2003 (structure data deposition date) |
Authors | Terasaka, T. / Okumura, H. / Tsuji, K. / Kato, T. / Nakanishi, I. / Kinoshita, T. / Kato, Y. / Kuno, M. / Seki, N. / Naoe, Y. ...Terasaka, T. / Okumura, H. / Tsuji, K. / Kato, T. / Nakanishi, I. / Kinoshita, T. / Kato, Y. / Kuno, M. / Seki, N. / Naoe, Y. / Inoue, T. / Tanaka, K. / Nakamura, K. |
External links | J. Med. Chem. / PubMed:15139750 |
Methods | X-ray diffraction |
Resolution | 2.5 Å |
Structure data | PDB-1v79: PDB-1v7a: PDB-2e1w: |
Chemicals | ChemComp-ZN: ChemComp-FR7: ChemComp-HOH: ChemComp-FRC: ChemComp-FR6: |
Source |
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Keywords | HYDROLASE / beta barrel / zinc |