Protein Secondary Structure Prediction Using Deep Convolutional Neural Fields

被引:313
|
作者
Wang, Sheng [1 ,2 ]
Peng, Jian [3 ]
Ma, Jianzhu [1 ]
Xu, Jinbo [1 ]
机构
[1] Toyota Technol Inst, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
[3] Univ Illinois, Dept Comp Sci, Urbana, IL USA
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
美国国家科学基金会;
关键词
MULTIPLE SEQUENCE ALIGNMENT; SOLVENT ACCESSIBILITY; ACCURACY; CLUSTAL; REGIONS; SERVER; MODEL;
D O I
10.1038/srep18962
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Protein secondary structure (SS) prediction is important for studying protein structure and function. When only the sequence (profile) information is used as input feature, currently the best predictors can obtain similar to 80% Q3 accuracy, which has not been improved in the past decade. Here we present DeepCNF (Deep Convolutional Neural Fields) for protein SS prediction. DeepCNF is a Deep Learning extension of Conditional Neural Fields (CNF), which is an integration of Conditional Random Fields (CRF) and shallow neural networks. DeepCNF can model not only complex sequence-structure relationship by a deep hierarchical architecture, but also interdependency between adjacent SS labels, so it is much more powerful than CNF. Experimental results show that DeepCNF can obtain similar to 84% Q3 accuracy, similar to 85% SOV score, and similar to 72% Q8 accuracy, respectively, on the CASP and CAMEO test proteins, greatly outperforming currently popular predictors. As a general framework, DeepCNF can be used to predict other protein structure properties such as contact number, disorder regions, and solvent accessibility.
引用
收藏
页数:11
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