基于对接计算的蛋白质- rna相互作用预测方法。

Masahito Ohue, Yuri Matsuzaki, Yutaka Akiyama
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引用次数: 0

摘要

阐明蛋白质- rna相互作用(PRIs)对于理解许多细胞系统是重要的。我们利用刚体蛋白- rna对接计算和三级结构数据建立了PRI预测方法。我们使用来自蛋白质数据库的78个蛋白质- rna复合物结构来评估这种方法。我们预测了78×78组合中对的相互作用。其中78个原始配合物被定义为正对,另外6006个被定义为负对;则该预测系统的f测量值为0.465。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Docking-calculation-based method for predicting protein-RNA interactions.

Elucidating protein-RNA interactions (PRIs) is important for understanding many cellular systems. We developed a PRI prediction method by using a rigid-body protein-RNA docking calculation with tertiary structure data. We evaluated this method by using 78 protein-RNA complex structures from the Protein Data Bank. We predicted the interactions for pairs in 78×78 combinations. Of these, 78 original complexes were defined as positive pairs, and the other 6,006 complexes were defined as negative pairs; then an F-measure value of 0.465 was obtained with our prediction system.

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