1CAH
STRUCTURE OF COBALT CARBONIC ANHYDRASE COMPLEXED WITH BICARBONATE
1CAH の概要
エントリーDOI | 10.2210/pdb1cah/pdb |
分子名称 | CARBONIC ANHYDRASE II, COBALT (II) ION, BICARBONATE ION, ... (4 entities in total) |
機能のキーワード | lyase(oxo-acid) |
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 | 29277.81 |
構造登録者 | |
主引用文献 | Hakansson, K.,Wehnert, A. Structure of cobalt carbonic anhydrase complexed with bicarbonate. J.Mol.Biol., 228:1212-1218, 1992 Cited by PubMed Abstract: The three-dimensional structure of a complex between catalytically active cobalt(II) substituted human carbonic anhydrase II and its substrate bicarbonate was determined by X-ray crystallography (1.9 A). One water molecule and two bicarbonate oxygen atoms are found at distances between 2.3 and 2.5 A from the cobalt ion in addition to the three histidyl ligands contributed by the peptide chain. The tetrahedral geometry around the metal ion in the native enzyme with a single water molecule 2.0 A from the metal is therefore lost. The geometry is difficult to classify but might best be described as distorted octahedral. The structure is suggested to represent a water-bicarbonate exchange state relevant also for native carbonic anhydrase, where the two unprotonized oxygen atoms of the substrate are bound in a carboxylate binding site and the hydroxyl group is free to move closer to the metal thereby replacing the metal-bound water molecule. A reaction mechanism based on crystallographically determined enzyme-ligand complexes is represented. PubMed: 1474587DOI: 10.1016/0022-2836(92)90327-G 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.88 Å) |
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