Convolutional neural networks with image representation of amino acid sequences for protein function prediction

2021 ◽  
Vol 92 ◽  
pp. 107494
Author(s):  
Samia Tasnim Sara ◽  
Md Mehedi Hasan ◽  
Ahsan Ahmad ◽  
Swakkhar Shatabda
2021 ◽  
Vol 95 ◽  
pp. 107584
Author(s):  
Mohamed E.M. Elhaj-Abdou ◽  
Hassan El-Dib ◽  
Amr El-Helw ◽  
Mohamed El-Habrouk

2021 ◽  
pp. 7831-7845
Author(s):  
Raghad Monther Eid, Eman K. Elsayed, Fatma T. Ghanam

Introduction: SARS-CoV-2 has become a worldwide pandemic that affects all aspects of life; therefore, numerous organizations and open exploration foundations focus their efforts on research for viable therapeutics. Given past experiences and involvement in SARS, the essential focus has been the Spike protein, considered as the perfect objective for COVID-19 immunotherapies. Most of the vaccines being developed target the spike proteins because this protein covers the virus and helps it invade human cells. Methods: Applications of deep neural network is a quickly expanding field now reaching many areas including proteomics. Results: To be precise, convolutional neural networks have been used for identifying the functional role of amino acid sequences, because of its ability to give nearly accurate results for multi-label classification problems. Here we present a modified convolutional deep learning model that can  identify if a given amino acid sequence is a spike protein or not based on the length of the sequence and the function of the protein, that will be done  with a short execution time and a relatively small error rate. Conclusion: CNN is an efficient tool at supervised multilabel classification problems


PeerJ ◽  
2018 ◽  
Vol 6 ◽  
pp. e4750 ◽  
Author(s):  
Afshine Amidi ◽  
Shervine Amidi ◽  
Dimitrios Vlachakis ◽  
Vasileios Megalooikonomou ◽  
Nikos Paragios ◽  
...  

During the past decade, with the significant progress of computational power as well as ever-rising data availability, deep learning techniques became increasingly popular due to their excellent performance on computer vision problems. The size of the Protein Data Bank (PDB) has increased more than 15-fold since 1999, which enabled the expansion of models that aim at predicting enzymatic function via their amino acid composition. Amino acid sequence, however, is less conserved in nature than protein structure and therefore considered a less reliable predictor of protein function. This paper presents EnzyNet, a novel 3D convolutional neural networks classifier that predicts the Enzyme Commission number of enzymes based only on their voxel-based spatial structure. The spatial distribution of biochemical properties was also examined as complementary information. The two-layer architecture was investigated on a large dataset of 63,558 enzymes from the PDB and achieved an accuracy of 78.4% by exploiting only the binary representation of the protein shape. Code and datasets are available at https://github.com/shervinea/enzynet.


2018 ◽  
Author(s):  
Cen Wan ◽  
Domenico Cozzetto ◽  
Rui Fa ◽  
David T. Jones

Protein-protein interaction network data provides valuable information that infers direct links between genes and their biological roles. This information brings a fundamental hypothesis for protein function prediction that interacting proteins tend to have similar functions. With the help of recently-developed network embedding feature generation methods and deep maxout neural networks, it is possible to extract functional representations that encode direct links between protein-protein interactions information and protein function. Our novel method, STRING2GO, successfully adopts deep maxout neural networks to learn functional representations simultaneously encoding both protein-protein interactions and functional predictive information. The experimental results show that STRING2GO outperforms other network embedding-based prediction methods and one benchmark method adopted in a recent large scale protein function prediction competition.


2020 ◽  
Vol 36 (11) ◽  
pp. 3343-3349 ◽  
Author(s):  
Manaz Kaleel ◽  
Yandan Zheng ◽  
Jialiang Chen ◽  
Xuanming Feng ◽  
Jeremy C Simpson ◽  
...  

Abstract Motivation The subcellular location of a protein can provide useful information for protein function prediction and drug design. Experimentally determining the subcellular location of a protein is an expensive and time-consuming task. Therefore, various computer-based tools have been developed, mostly using machine learning algorithms, to predict the subcellular location of proteins. Results Here, we present a neural network-based algorithm for protein subcellular location prediction. We introduce SCLpred-EMS a subcellular localization predictor powered by an ensemble of Deep N-to-1 Convolutional Neural Networks. SCLpred-EMS predicts the subcellular location of a protein into two classes, the endomembrane system and secretory pathway versus all others, with a Matthews correlation coefficient of 0.75–0.86 outperforming the other state-of-the-art web servers we tested. Availability and implementation SCLpred-EMS is freely available for academic users at http://distilldeep.ucd.ie/SCLpred2/. Contact [email protected]


2021 ◽  
Author(s):  
Theo Sanderson ◽  
Maxwell L Bileschi ◽  
David Belanger ◽  
Lucy Colwell

Predicting the function of a protein from its amino acid sequence is a long-standing challenge in bioinformatics. Traditional approaches use sequence alignment to compare a query sequence either to thousands of models of protein families or to large databases of individual protein sequences. Here we instead employ deep convolutional neural networks to directly predict a variety of protein functions -- EC numbers and GO terms -- directly from an unaligned amino acid sequence. This approach provides precise predictions which complement alignment-based methods, and the computational efficiency of a single neural network permits novel and lightweight software interfaces, which we demonstrate with an in-browser graphical interface for protein function prediction in which all computation is performed on the user's personal computer with no data uploaded to remote servers. Moreover, these models place full-length amino acid sequences into a generalised functional space, facilitating downstream analysis and interpretation. To read the interactive version of this paper, visit https://google-research.github.io/proteinfer/


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