scholarly journals Predicting Protein Functions from Protein Interaction Networks

2009 ◽  
pp. 203-222 ◽  
Author(s):  
Hon Nian Chua ◽  
Limsoon Wong
Keyword(s):  
Protein Interaction ◽  
Protein Function ◽  
Protein Function Prediction ◽  
Functional Characterization ◽  
Function Prediction ◽  
Functional Annotations ◽  
Protein Protein Interaction ◽  
Protein Functions ◽  
High Throughput Manner

Functional characterization of genes and their protein products is essential to biological and clinical research. Yet, there is still no reliable way of assigning functional annotations to proteins in a high-throughput manner. In this chapter, the authors provide an introduction to the task of automated protein function prediction. They discuss about the motivation for automated protein function prediction, the challenges faced in this task, as well as some approaches that are currently available. In particular, they take a closer look at methods that use protein-protein interaction for protein function prediction, elaborating on their underlying techniques and assumptions, as well as their strengths and limitations.

scholarly journals Predicting Protein Functions from Protein Interaction Networks

2012 ◽  
Vol 3 (4) ◽  
pp. 50-70 ◽  
Author(s):  
Hon Nian Chua ◽  
Limsoon Wong
Keyword(s):  
Protein Interaction ◽  
Protein Function ◽  
Protein Function Prediction ◽  
Functional Characterization ◽  
Function Prediction ◽  
Functional Annotations ◽  
Protein Protein Interaction ◽  
Protein Functions ◽  
High Throughput Manner

Functional characterization of genes and their protein products is essential to biological and clinical research. Yet, there is still no reliable way of assigning functional annotations to proteins in a high-throughput manner. In this article, the authors provide an introduction to the task of automated protein function prediction. They discuss about the motivation for automated protein function prediction, the challenges faced in this task, as well as some approaches that are currently available. In particular, they take a closer look at methods that use protein-protein interaction for protein function prediction, elaborating on their underlying techniques and assumptions, as well as their strengths and limitations.

DYNAMICALLY SEARCHING FOR A DOMAIN FOR PROTEIN FUNCTION PREDICTION

2013 ◽  
Vol 11 (04) ◽  
pp. 1350008 ◽  
Author(s):  
JINGYU HOU ◽  
YONGQING JIANG
Keyword(s):  
Protein Function ◽  
Structural Information ◽  
Protein Function Prediction ◽  
Function Prediction ◽  
Computational Approaches ◽  
Protein Protein Interaction ◽  
Protein Functions ◽  
Novel Method ◽  
Function Information ◽  
The Relationship

The availability of large amounts of protein–protein interaction (PPI) data makes it feasible to use computational approaches to predict protein functions. The base of existing computational approaches is to exploit the known function information of annotated proteins in the PPI data to predict functions of un-annotated proteins. However, these approaches consider the prediction domain (i.e. the set of proteins from which the functions are predicted) as unchangeable during the prediction procedure. This may lead to valuable information being overwhelmed by the unavoidable noise information in the PPI data when predicting protein functions, and in turn, the prediction results will be distorted. In this paper, we propose a novel method to dynamically predict protein functions from the PPI data. Our method regards the function prediction as a dynamic process of finding a suitable prediction domain, from which representative functions of the domain are selected to predict functions of un-annotated proteins. Our method exploits the topological structural information of a PPI network and the semantic relationship between protein functions to measure the relationship between proteins, dynamically select a suitable prediction domain and predict functions. The evaluation on real PPI datasets demonstrated the effectiveness of our proposed method, and generated better prediction results.

COMPUTATIONAL METHOD FOR PROTEIN FUNCTION PREDICTION BY CONSTRUCTING PROTEIN INTERACTION NETWORK DICTIONARY

2006 ◽  
Vol 20 (02) ◽  
pp. 285-295 ◽  
Author(s):  
HEE-JEONG JIN ◽  
HWAN-GUE CHO
Keyword(s):  
Protein Interaction ◽  
Protein Interaction Network ◽  
Protein Function ◽  
Protein Function Prediction ◽  
Interaction Network ◽  
Computational Method ◽  
Chi Square ◽  
Protein Protein Interaction ◽  
Protein Functions ◽  
Novel Method

In the post-genomic era, predicting protein function is a challenging problem. It is difficult and burdensome work to unravel the functions of a protein by wet experiments only. In this paper, we propose a novel method to predict protein functions by building a "Protein Interaction Network Dictionary (PIND)". This method deduces the protein functions by searching the most similar "words"(an anagram of functions in neighbor proteins on a protein–protein interaction graph) using global alignments. An evaluation of sensitivity and specificity shows that this PIND approach outperforms previous approaches such as Majority Rule and Chi-Square measure, and that it competes with the recently introduced Random Markov Model approach.

scholarly journals FunPred 3.0: improved protein function prediction using protein interaction network

PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e6830 ◽  
Author(s):  
Sovan Saha ◽  
Piyali Chatterjee ◽  
Subhadip Basu ◽  
Mita Nasipuri ◽  
Dariusz Plewczynski
Keyword(s):  
Protein Interaction ◽  
Protein Interactions ◽  
Protein Interaction Network ◽  
Protein Function ◽  
Protein Function Prediction ◽  
Experimental Studies ◽  
Interaction Network ◽  
Function Prediction ◽  
The Self ◽  
Functional Annotations

Proteins are the most versatile macromolecules in living systems and perform crucial biological functions. In the advent of the post-genomic era, the next generation sequencing is done routinely at the population scale for a variety of species. The challenging problem is to massively determine the functions of proteins that are yet not characterized by detailed experimental studies. Identification of protein functions experimentally is a laborious and time-consuming task involving many resources. We therefore propose the automated protein function prediction methodology using in silico algorithms trained on carefully curated experimental datasets. We present the improved protein function prediction tool FunPred 3.0, an extended version of our previous methodology FunPred 2, which exploits neighborhood properties in protein–protein interaction network (PPIN) and physicochemical properties of amino acids. Our method is validated using the available functional annotations in the PPIN network of Saccharomyces cerevisiae in the latest Munich information center for protein (MIPS) dataset. The PPIN data of S. cerevisiae in MIPS dataset includes 4,554 unique proteins in 13,528 protein–protein interactions after the elimination of the self-replicating and the self-interacting protein pairs. Using the developed FunPred 3.0 tool, we are able to achieve the mean precision, the recall and the F-score values of 0.55, 0.82 and 0.66, respectively. FunPred 3.0 is then used to predict the functions of unpredicted protein pairs (incomplete and missing functional annotations) in MIPS dataset of S. cerevisiae. The method is also capable of predicting the subcellular localization of proteins along with its corresponding functions. The code and the complete prediction results are available freely at: https://github.com/SovanSaha/FunPred-3.0.git.

scholarly journals DeepGOPlus: improved protein function prediction from sequence

2019 ◽  
Author(s):  
Maxat Kulmanov ◽  
Robert Hoehndorf
Keyword(s):  
Protein Function ◽  
Drug Targets ◽  
Sequence Similarity ◽  
Protein Function Prediction ◽  
Function Prediction ◽  
Supplementary Information ◽  
Protein Protein Interaction ◽  
Wide Range ◽  
Protein Functions ◽  
Novel Method

Abstract Motivation Protein function prediction is one of the major tasks of bioinformatics that can help in wide range of biological problems such as understanding disease mechanisms or finding drug targets. Many methods are available for predicting protein functions from sequence based features, protein–protein interaction networks, protein structure or literature. However, other than sequence, most of the features are difficult to obtain or not available for many proteins thereby limiting their scope. Furthermore, the performance of sequence-based function prediction methods is often lower than methods that incorporate multiple features and predicting protein functions may require a lot of time. Results We developed a novel method for predicting protein functions from sequence alone which combines deep convolutional neural network (CNN) model with sequence similarity based predictions. Our CNN model scans the sequence for motifs which are predictive for protein functions and combines this with functions of similar proteins (if available). We evaluate the performance of DeepGOPlus using the CAFA3 evaluation measures and achieve an Fmax of 0.390, 0.557 and 0.614 for BPO, MFO and CCO evaluations, respectively. These results would have made DeepGOPlus one of the three best predictors in CCO and the second best performing method in the BPO and MFO evaluations. We also compare DeepGOPlus with state-of-the-art methods such as DeepText2GO and GOLabeler on another dataset. DeepGOPlus can annotate around 40 protein sequences per second on common hardware, thereby making fast and accurate function predictions available for a wide range of proteins. Availability and implementation http://deepgoplus.bio2vec.net/. Supplementary information Supplementary data are available at Bioinformatics online.

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