3M96
Crystal structure of human carbonic anhydrase isozyme II with 5-{[(5-bromo-1H-benzimidazol-2-yl)sulfanyl]acetyl}-2-chlorobenzenesulfonamide
Summary for 3M96
Entry DOI | 10.2210/pdb3m96/pdb |
Related | 3M98 |
Descriptor | Carbonic anhydrase 2, ZINC ION, DIMETHYL SULFOXIDE, ... (5 entities in total) |
Functional Keywords | drug design, carbonic anhydrase, benzenesulfonamide, lyase |
Biological source | Homo sapiens (human) |
Cellular location | Cytoplasm : P00918 |
Total number of polymer chains | 1 |
Total formula weight | 29971.49 |
Authors | Grazulis, S.,Manakova, E.,Golovenko, D. (deposition date: 2010-03-20, release date: 2011-02-02, Last modification date: 2023-09-06) |
Primary citation | 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 (1.4 Å) |
Structure validation
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