7ORP
crystal structure of human carbonic anhydrase II in complex with 4-((2-hydroxy-3-((3,4,5-trimethoxyphenyl)tellanyl)propyl)selanyl)benzenesulfonamide
This is a non-PDB format compatible entry.
Summary for 7ORP
Entry DOI | 10.2210/pdb7orp/pdb |
Descriptor | Carbonic anhydrase 2, ZINC ION, GLYCEROL, ... (6 entities in total) |
Functional Keywords | carbonic anhydrase ii, inhibitor, organoselenium, sulfonamide, metalloenzyme, lyase |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 30622.57 |
Authors | Angeli, A.,Ferraroni, M. (deposition date: 2021-06-06, release date: 2022-06-22, Last modification date: 2024-02-07) |
Primary citation | Tanini, D.,Carradori, S.,Capperucci, A.,Lupori, L.,Zara, S.,Ferraroni, M.,Ghelardini, C.,Mannelli, L.,Micheli, L.,Lucarini, E.,Carta, F.,Angeli, A.,Supuran, C.T. Chalcogenides-incorporating carbonic anhydrase inhibitors concomitantly reverted oxaliplatin-induced neuropathy and enhanced antiproliferative action. Eur.J.Med.Chem., 225:113793-113793, 2021 Cited by PubMed: 34507012DOI: 10.1016/j.ejmech.2021.113793 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.43 Å) |
Structure validation
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