Moras D
Institut de Biologie, Moléculaire et Cellulaire du CNRS, Laboratoire de Cristallographie Biologique, Strasbourg, France.
Trends Biochem Sci. 1992 Apr;17(4):159-64. doi: 10.1016/0968-0004(92)90326-5.
Aminoacyl-tRNA synthetases can be divided in two groups of equal size on the basis of differences in the structure of their active sites. The core of class I synthetases is the classical nucleotide-binding domain with its characteristic Rossmann fold. In contrast, the active site of class II synthetases is built around an antiparallel beta-sheet, to which the substrates bind. This classification, which is based on structural data (amino acid sequences and tertiary structures), can be rationalized in functional terms.
氨酰-tRNA合成酶可根据其活性位点结构的差异分为大小相等的两组。I类合成酶的核心是具有特征性Rossmann折叠的经典核苷酸结合结构域。相比之下,II类合成酶的活性位点围绕着一个反平行β-折叠构建,底物与之结合。这种基于结构数据(氨基酸序列和三级结构)的分类可以从功能角度进行合理说明。