The goal of Protein Structure Prediction (PSP) problem is to predict a protein's 3D structure (confirmation) from its amino acid sequence. The problem has been a 'holy grail' of science since the Noble prize-winning work of Anfinsen demonstrated that protein conformation was determined by sequence. A recent and important step towards this goal was the development of AlphaFold2, currently the best PSP method. AlphaFold2 is probably the highest profile application of AI to science. Both AlphaFold2 and RoseTTAFold (another impressive PSP method) have been published and placed in the public domain (code & models). Stacking is a form of ensemble machine learning ML in which multiple baseline models are first learnt, then a meta-model is learnt using the outputs of the baseline level model to form a model that outperforms the base models. Stacking has been successful in many applications. We developed the ARStack PSP method by stacking AlphaFold2 and RoseTTAFold. ARStack significantly outperforms AlphaFold2. We rigorously demonstrate this using two sets of non-homologous proteins, and a test set of protein structures published after that of AlphaFold2 and RoseTTAFold. As more high quality prediction methods are published it is likely that ensemble methods will increasingly outperform any single method.
翻译:蛋白质结构预测(PSP)问题的目标是从蛋白质氨酸序列中预测蛋白质的3D结构(确认) 。 问题在于自获诺贝尔奖的安芬森(Anfinsen)的工作显示蛋白质符合性是由序列决定的。 最近的一个重要步骤是开发了目前最佳的 PSP 方法。 AlphaFold2 可能是AI 对科学的最高应用。 AlphaFold2 和 RoseTTAFoldold (另一种令人印象深刻的 PSP 方法) 已经公布并放置在公共领域( 代码和模型 ) 。 自诺贝尔奖获奖奖的安芬森( Anfinsen) 的工作显示蛋白质符合序列。 最近的一个重要步骤是开发了阿尔法Fold2 和 RoseFold 的3DSP 方法( 另一种令人印象深刻的 PSP 方法 ) 。 ASBack 明显地超越了 ASBAFold 学习MLM 。 我们日益使用多种标准方法来演示它。