3P55
Human carbonic anhydrase II in complex with p-(4-ferrocenyl-1H-1,2,3-triazol-1-yl)benzenesulfonamide
3P55 の概要
| エントリーDOI | 10.2210/pdb3p55/pdb |
| 分子名称 | Carbonic anhydrase 2, p-(4-ferrocenyl-1H-1,2,3-triazol-1-yl)benzenesulfonamide, GLYCEROL, ... (5 entities in total) |
| 機能のキーワード | carbonic anhydrase alpha, lyase, cytosolic |
| 由来する生物種 | Homo sapiens (human) |
| 細胞内の位置 | Cytoplasm: P00918 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 29938.85 |
| 構造登録者 | |
| 主引用文献 | Salmon, A.J.,Williams, M.L.,Hofmann, A.,Poulsen, S.A. Protein crystal structures with ferrocene and ruthenocene-based enzyme inhibitors. Chem.Commun.(Camb.), 48:2328-2330, 2012 Cited by PubMed Abstract: We have determined the protein X-ray crystal structures of four organometallic inhibitors in complex with their target enzyme carbonic anhydrase II. The barrel-shaped hydrophobic ferrocene and ruthenocene moieties have provided a structure-based avenue to better occupy the hydrophobic binding patch within the enzyme active site. PubMed: 22258283DOI: 10.1039/c2cc15625c 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2 Å) |
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