3M2N
Crystal structure of human carbonic anhydrase isozyme II with 4-{2-[N-(6-chloro-5-nitropyrimidin-4-yl)amino]ethyl}benzenesulfonamide
Summary for 3M2N
Entry DOI | 10.2210/pdb3m2n/pdb |
Related | 3M3X 3M40 3M5E 3MHI 3MHL 3MHM 3MHO |
Descriptor | Carbonic anhydrase 2, 4-{2-[(6-chloro-5-nitropyrimidin-4-yl)amino]ethyl}benzenesulfonamide, ZINC ION, ... (6 entities in total) |
Functional Keywords | drug design, carbonic anhydrase, sulfonamide, lyase, 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 | 30031.68 |
Authors | Grazulis, S.,Manakova, E.,Golovenko, D. (deposition date: 2010-03-08, release date: 2011-02-16, Last modification date: 2023-11-01) |
Primary citation | Capkauskaite, E.,Zubriene, A.,Baranauskiene, L.,Tamulaitiene, G.,Manakova, E.,Kairys, V.,Grazulis, S.,Tumkevicius, S.,Matulis, D. Design of [(2-pyrimidinylthio)acetyl]benzenesulfonamides as inhibitors of human carbonic anhydrases. Eur.J.Med.Chem., 51:259-270, 2012 Cited by PubMed: 22440859DOI: 10.1016/j.ejmech.2012.02.050 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.65 Å) |
Structure validation
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