Department of Chemistry, University of California, Davis, One Shields Avenue, Davis, California 95616, United States.
Department of Biomedical Engineering, University of California, Davis, Davis, California 95616, United States.
Biochemistry. 2020 Oct 13;59(40):3834-3843. doi: 10.1021/acs.biochem.0c00665. Epub 2020 Sep 23.
To complement established rational and evolutionary protein design approaches, significant efforts are being made to utilize computational modeling and the diversity of naturally occurring protein sequences. Here, we combine structural biology, genomic mining, and computational modeling to identify structural features critical to aldehyde deformylating oxygenases (ADOs), an enzyme family that has significant implications in synthetic biology and chemoenzymatic synthesis. Through these efforts, we discovered latent ADO-like function across the ferritin-like superfamily in various species of Bacteria and Archaea. We created a machine learning model that uses protein structural features to discriminate ADO-like activity. Computational enzyme design tools were then utilized to introduce ADO-like activity into the small subunit of class I ribonucleotide reductase. The integrated approach of genomic mining, structural biology, molecular modeling, and machine learning has the potential to be utilized for rapid discovery and modulation of functions across enzyme families.
为了补充已建立的理性和进化蛋白质设计方法,人们正在大力利用计算建模和自然发生的蛋白质序列的多样性。在这里,我们结合结构生物学、基因组挖掘和计算建模来确定醛脱甲酰基氧化酶(ADOs)的关键结构特征,ADOs 是一个在合成生物学和化学酶合成中具有重要意义的酶家族。通过这些努力,我们在各种细菌和古菌的铁蛋白样超家族中发现了潜在的 ADO 样功能。我们创建了一个使用蛋白质结构特征来区分 ADO 样活性的机器学习模型。然后利用计算酶设计工具将 ADO 样活性引入到 I 类核糖核苷酸还原酶的小亚基中。基因组挖掘、结构生物学、分子建模和机器学习的综合方法有可能被用于快速发现和调节酶家族的功能。