4HT0
Crystal structure of human carbonic anhydrase isozyme II with the inhibitor.
Summary for 4HT0
Entry DOI | 10.2210/pdb4ht0/pdb |
Descriptor | Carbonic anhydrase 2, ZINC ION, 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, ... (6 entities in total) |
Functional Keywords | drug design, carbonic anhydrase, benzenesulfonamide, metal-binding, lyase-lyase inhibitor complex, carbon-oxygen lyase activity, lyase/lyase inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Cytoplasm : P00918 |
Total number of polymer chains | 1 |
Total formula weight | 29995.18 |
Authors | Smirnov, A.,Manakova, E.,Grazulis, S. (deposition date: 2012-10-31, release date: 2013-04-10, Last modification date: 2023-09-20) |
Primary citation | Dudutiene, V.,Zubriene, A.,Smirnov, A.,Gylyte, J.,Timm, D.,Manakova, E.,Grazulis, S.,Matulis, D. 4-Substituted-2,3,5,6-tetrafluorobenzenesulfonamides as inhibitors of carbonic anhydrases I, II, VII, XII, and XIII. Bioorg.Med.Chem., 21:2093-2106, 2013 Cited by PubMed: 23394791DOI: 10.1016/j.bmc.2013.01.008 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.6 Å) |
Structure validation
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