4Q6E
Crystal structure of human carbonic anhydrase isozyme II with 4-{[3-(3,5-Dimethyl-1H-pyrazol-1-yl)-3-oxopropyl]amino}benzene-1-sulfonamide
Summary for 4Q6E
Entry DOI | 10.2210/pdb4q6e/pdb |
Related | 4Q6D |
Descriptor | Carbonic anhydrase 2, ZINC ION, BICINE, ... (6 entities in total) |
Functional Keywords | drug design, carbonic anhydrase, benzenesulfonamide, metal-binding, lyase-lyase inhibitor complex, lyase/lyase inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Cytoplasm : P00918 |
Total number of polymer chains | 1 |
Total formula weight | 29996.29 |
Authors | Smirnov, A.,Manakova, E.,Grazulis, S. (deposition date: 2014-04-22, release date: 2014-11-26, Last modification date: 2023-09-20) |
Primary citation | Rutkauskas, K.,Zubriene, A.,Tumosiene, I.,Kantminiene, K.,Kazemekaite, M.,Smirnov, A.,Kazokaite, J.,Morkunaite, V.,Capkauskaite, E.,Manakova, E.,Grazulis, S.,Beresnevicius, Z.J.,Matulis, D. 4-Amino-substituted Benzenesulfonamides as Inhibitors of Human Carbonic Anhydrases. Molecules, 19:17356-17380, 2014 Cited by PubMed: 25353386DOI: 10.3390/molecules191117356 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.12 Å) |
Structure validation
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