CNNsite: Prediction of DNA-binding residues in proteins using Convolutional Neural Network with sequence features

Jiyun Zhou, Q. Lu, Ruifeng Xu, Lin Gui, Hongpeng Wang
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引用次数: 29

Abstract

Protein-DNA complexes play crucial roles in gene regulation. The prediction of the residues involved in protein-DNA interactions is critical for understanding gene regulation. Although many methods have been proposed, most of them overlooked motif features. Motif features are sub sequences and are important for the recognition between a protein and DNA. In order to efficiently use motif features for the prediction of DNA-binding residues, we first apply the Convolutional Neural Network (CNN) method to capture the motif features from the sequences around the target residues. CNN modeling consists of a set of learnable motif detectors that can capture the important motif features by scanning the sequences around the target residues. Then we use a neural network classifier, referred to as CNNsite, by combining the captured motif features, sequence features and evolutionary features to predict binding residues from sequences. The datasets PDNA-62 and PDNA-224 are used to evaluate the performance of CNNsite by five-fold cross-validation. Performance evaluation shows that the motif features performs better than sequence features and evolutionary features with at least 6.73% on ST, 0.097 on MCC and 0.069 on AUC. When comparing with previously published methods, CNNsite performs better with at least 0.019 on MCC, 4.37% on ST and 0.040 on AUC. CNNsite is also evaluated on an independent dataset TS-72 and CNNsite outperforms the previous methods by at least 0.012 on AUC. The discriminant powers of the motif features of size from 2 to 6 residues show that many motif features with large discriminant power are composed by the residues that play important roles in the DNA-protein interactions. The standalone version of the CNNsite is available at http://hlt.hitsz.edu.cn:8080/CNNsite/.
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CNNsite:利用具有序列特征的卷积神经网络预测蛋白质中的dna结合残基
蛋白质- dna复合物在基因调控中起着至关重要的作用。预测参与蛋白质- dna相互作用的残基对于理解基因调控至关重要。虽然提出了许多方法,但大多数方法都忽略了基序特征。基序特征是亚序列,对蛋白质和DNA之间的识别非常重要。为了有效地利用基序特征预测dna结合残基,我们首先应用卷积神经网络(CNN)方法从目标残基周围的序列中捕获基序特征。CNN建模由一组可学习的motif检测器组成,这些检测器可以通过扫描目标残基周围的序列来捕获重要的motif特征。然后,我们使用神经网络分类器,即CNNsite,通过结合捕获的基序特征、序列特征和进化特征来预测序列的结合残基。使用数据集PDNA-62和PDNA-224对CNNsite进行五重交叉验证。性能评价表明,motif特征在ST、MCC和AUC上的识别率分别为6.73%、0.097和0.069,优于序列特征和进化特征。与之前发表的方法相比,CNNsite在MCC上的表现更好,在ST上的表现至少为0.019,在AUC上的表现为4.37%,在AUC上的表现为0.040。CNNsite也在一个独立的数据集TS-72上进行了评估,CNNsite在AUC上比之前的方法至少高出0.012。2 ~ 6个残基大小的基序特征的判别能力表明,许多具有较大判别能力的基序特征是由在dna -蛋白质相互作用中起重要作用的残基组成的。CNNsite的独立版本可在http://hlt.hitsz.edu.cn:8080/CNNsite/上获得。
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