3SAP
Crystal structure of human carbonic anhydrase isozyme II with 4-{[(5-butyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide
Summary for 3SAP
Entry DOI | 10.2210/pdb3sap/pdb |
Related | 3S8X 3S9T 3SAX 3SBH 3SBI |
Descriptor | Carbonic anhydrase 2, ZINC ION, BICINE, ... (7 entities in total) |
Functional Keywords | drug design, sulfonamide, 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 | 30156.48 |
Authors | Grazulis, S.,Manakova, E.,Tamulaitiene, G. (deposition date: 2011-06-03, release date: 2012-04-11, Last modification date: 2023-09-13) |
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 (1.75 Å) |
Structure validation
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