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| Title | Carbonic anhydrase inhibitors: The X-ray crystal structure of the adduct of N-hydroxysulfamide with isozyme II explains why this new zinc binding function is effective in the design of potent inhibitors. |
|---|---|
| Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 17, Page 2795-2801, Year 2007 |
| Publish date | Dec 5, 2006 (structure data deposition date) |
Authors | Temperini, C. / Winum, J.Y. / Montero, J.L. / Scozzafava, A. / Supuran, C.T. |
External links | Bioorg. Med. Chem. Lett. / PubMed:17346964 |
| Methods | X-ray diffraction |
| Resolution | 2.1 Å |
| Structure data | ![]() PDB-2o4z: |
| Chemicals | ![]() ChemComp-ZN: ![]() ChemComp-HG: ![]() ChemComp-HSW: ![]() ChemComp-HOH: |
| Source |
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Keywords | LYASE / carbonic anhydrase / inhibitors |
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