4KP8
Crystal structure of catalytic domain of human carbonic anhydrase isozyme XII with 3-[(Pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide
Summary for 4KP8
Entry DOI | 10.2210/pdb4kp8/pdb |
Related | 4KNI 4KNJ 4KNM 4KNN 4KP5 |
Descriptor | Carbonic anhydrase 12, ZINC ION, 3-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide, ... (7 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 | Membrane; Single-pass type I membrane protein: O43570 |
Total number of polymer chains | 4 |
Total formula weight | 121211.44 |
Authors | Smirnov, A.,Manakova, E.,Grazulis, S. (deposition date: 2013-05-13, release date: 2013-11-06, Last modification date: 2023-11-08) |
Primary citation | Capkauskaite, E.,Zubriene, A.,Smirnov, A.,Torresan, J.,Kisonaite, M.,Kazokaite, J.,Gylyte, J.,Michailoviene, V.,Jogaite, V.,Manakova, E.,Grazulis, S.,Tumkevicius, S.,Matulis, D. Benzenesulfonamides with pyrimidine moiety as inhibitors of human carbonic anhydrases I, II, VI, VII, XII, and XIII Bioorg.Med.Chem., 21:6937-6947, 2013 Cited by PubMed: 24103428DOI: 10.1016/j.bmc.2013.09.029 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.8 Å) |
Structure validation
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