Holm L, Sander C
European Bioinformatics Institute, European Molecular Biology Laboratory, Cambridge, United Kingdom.
Proteins. 1997 May;28(1):72-82.
The recent determination of the three-dimensional structure of urease revealed striking similarities of enzyme architecture to adenosine deaminase and phosphotriesterase, evidence of a distant evolutionary relationship that had gone undetected by one-dimensional sequence comparisons. Here, based on an analysis of conservation patterns in three dimensions, we report the discovery of the same active-site architecture in an even larger set of enzymes involved primarily in nucleotide metabolism. As a consequence, we predict the three-dimensional fold and details of the active site architecture for dihydroorotases, allantoinases, hydantoinases, AMP-, adenine and cytosine deaminases, imidazolonepropionase, aryldialkylphosphatase, chlorohydrolases, formylmethanofuran dehydrogenases, and proteins involved in animal neuronal development. Two member families are common to archaea, eubacteria, and eukaryota. Thirteen other functions supported by the same structural motif and conserved chemical mechanism apparently represent later adaptations for different substrate specificities in different cellular contexts.
最近对脲酶三维结构的测定揭示了该酶结构与腺苷脱氨酶和磷酸三酯酶惊人的相似性,这一遥远的进化关系在一维序列比较中未被发现。在此,基于对三维保守模式的分析,我们报告在一组主要参与核苷酸代谢的更大的酶中发现了相同的活性位点结构。因此,我们预测了二氢乳清酸酶、尿囊素酶、乙内酰脲酶、AMP-、腺嘌呤和胞嘧啶脱氨酶、咪唑啉酮丙酸酶、芳基二烷基磷酸酶、氯水解酶、甲酰基甲烷呋喃脱氢酶以及参与动物神经发育的蛋白质的三维折叠和活性位点结构细节。两个成员家族在古细菌、真细菌和真核生物中是常见的。由相同结构基序和保守化学机制支持的其他十三种功能显然代表了在不同细胞环境中对不同底物特异性的后期适应性变化。