3M67
Crystal structure of human carbonic anhydrase isozyme II with 2-chloro-5-[(6,7-dihydro-1H-[1,4]dioxino[2,3-f]benzimidazol-2-ylsulfanyl)acetyl]benzenesulfonamide
Summary for 3M67
Entry DOI | 10.2210/pdb3m67/pdb |
Related | 3m2n 3m3x 3m40 3m5e |
Descriptor | Carbonic anhydrase 2, 2-chloro-5-[(6,7-dihydro-1H-[1,4]dioxino[2,3-f]benzimidazol-2-ylsulfanyl)acetyl]benzenesulfonamide, ZINC ION, ... (5 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 | 29950.63 |
Authors | Grazulis, S.,Manakova, E.,Golovenko, D. (deposition date: 2010-03-15, release date: 2010-11-03, Last modification date: 2023-11-01) |
Primary citation | Capkauskaite, E.,Baranauskiene, L.,Golovenko, D.,Manakova, E.,Grazulis, S.,Tumkevicius, S.,Matulis, D. Indapamide-like benzenesulfonamides as inhibitors of carbonic anhydrases I, II, VII, and XIII Bioorg.Med.Chem., 18:7357-7364, 2010 Cited by PubMed: 20926301DOI: 10.1016/j.bmc.2010.09.016 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.8 Å) |
Structure validation
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