Laboratory of Systems Pharmacology, Department of Systems Biology, Harvard Medical School, 200 Longwood Avenue, Boston, MA, 02115, USA.
BMC Bioinformatics. 2019 Jun 11;20(1):311. doi: 10.1186/s12859-019-2932-0.
Rapid progress in deep learning has spurred its application to bioinformatics problems including protein structure prediction and design. In classic machine learning problems like computer vision, progress has been driven by standardized data sets that facilitate fair assessment of new methods and lower the barrier to entry for non-domain experts. While data sets of protein sequence and structure exist, they lack certain components critical for machine learning, including high-quality multiple sequence alignments and insulated training/validation splits that account for deep but only weakly detectable homology across protein space.
We created the ProteinNet series of data sets to provide a standardized mechanism for training and assessing data-driven models of protein sequence-structure relationships. ProteinNet integrates sequence, structure, and evolutionary information in programmatically accessible file formats tailored for machine learning frameworks. Multiple sequence alignments of all structurally characterized proteins were created using substantial high-performance computing resources. Standardized data splits were also generated to emulate the difficulty of past CASP (Critical Assessment of protein Structure Prediction) experiments by resetting protein sequence and structure space to the historical states that preceded six prior CASPs. Utilizing sensitive evolution-based distance metrics to segregate distantly related proteins, we have additionally created validation sets distinct from the official CASP sets that faithfully mimic their difficulty.
ProteinNet represents a comprehensive and accessible resource for training and assessing machine-learned models of protein structure.
深度学习的快速发展推动了其在生物信息学问题中的应用,包括蛋白质结构预测和设计。在计算机视觉等经典机器学习问题中,进展得益于标准化数据集,这有利于公平评估新方法,并降低非专业人士的进入门槛。虽然存在蛋白质序列和结构的数据集,但它们缺乏机器学习关键的某些组件,包括高质量的多重序列比对和隔离的训练/验证分割,这些组件考虑了蛋白质空间中深度但仅微弱可检测的同源性。
我们创建了 ProteinNet 系列数据集,为训练和评估基于数据的蛋白质序列-结构关系模型提供了标准化机制。ProteinNet 以适合机器学习框架的可编程访问文件格式集成了序列、结构和进化信息。使用大量高性能计算资源创建了所有结构特征化蛋白质的多重序列比对。还生成了标准化数据分割,通过将蛋白质序列和结构空间重置为六个之前的 CASP 之前的历史状态,来模拟过去 CASP(蛋白质结构预测关键评估)实验的难度。利用基于敏感进化的距离度量来隔离远缘相关的蛋白质,我们还创建了与官方 CASP 集不同的验证集,忠实地模拟了它们的难度。
ProteinNet 代表了用于训练和评估蛋白质结构的基于机器学习模型的全面和可访问资源。