Binding Affinity Prediction Models for Spinocerebellar Ataxia Using Supervised Learning

2018 ◽  
pp. 145-152
Author(s):  
P. R. Asha ◽  
M. S. Vijaya
Keyword(s):  
Supervised Learning ◽  
Binding Affinity ◽  
Spinocerebellar Ataxia ◽  
Prediction Models ◽  
Binding Affinity Prediction ◽  
Affinity Prediction

scholarly journals Binding affinity prediction for protein–ligand complex using deep attention mechanism based on intermolecular interactions

2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Sangmin Seo ◽  
Jonghwan Choi ◽  
Sanghyun Park ◽  
Jaegyoon Ahn
Keyword(s):  
Deep Learning ◽  
Binding Affinity ◽  
Prediction Models ◽  
Attention Mechanism ◽  
Scoring Functions ◽  
Ligand Complex ◽  
Structure Based Drug Design ◽  
Binding Affinity Prediction ◽  
Affinity Prediction ◽  
Proposed Model

Abstract Background Accurate prediction of protein–ligand binding affinity is important for lowering the overall cost of drug discovery in structure-based drug design. For accurate predictions, many classical scoring functions and machine learning-based methods have been developed. However, these techniques tend to have limitations, mainly resulting from a lack of sufficient energy terms to describe the complex interactions between proteins and ligands. Recent deep-learning techniques can potentially solve this problem. However, the search for more efficient and appropriate deep-learning architectures and methods to represent protein–ligand complex is ongoing. Results In this study, we proposed a deep-neural network model to improve the prediction accuracy of protein–ligand complex binding affinity. The proposed model has two important features, descriptor embeddings with information on the local structures of a protein–ligand complex and an attention mechanism to highlight important descriptors for binding affinity prediction. The proposed model performed better than existing binding affinity prediction models on most benchmark datasets. Conclusions We confirmed that an attention mechanism can capture the binding sites in a protein–ligand complex to improve prediction performance. Our code is available at https://github.com/Blue1993/BAPA.

GRAM: A True Null Model for Relative Binding Affinity Predictions

2019 ◽  
Author(s):  
Guanglei Cui ◽  
Alan P. Graves ◽  
Eric S. Manas
Keyword(s):  
Binding Affinity ◽  
Performance Metrics ◽  
Null Model ◽  
Performance Measure ◽  
Interval Estimate ◽  
Empirical Observation ◽  
Binding Affinity Prediction ◽  
Affinity Prediction ◽  
Relative Binding Affinity ◽  
Relative Binding

Relative binding affinity prediction is a critical component in computer aided drug design. Significant amount of effort has been dedicated to developing rapid and reliable in silico methods. However, robust assessment of their performance is still a complicated issue, as it requires a performance measure applicable in the prospective setting and more importantly a true null model that defines the expected performance of random in an objective manner. Although many performance metrics, such as correlation coefficient (r2), mean unsigned error (MUE), and room mean square error (RMSE), are frequently used in the literature, a true and non-trivial null model has yet been identified. To address this problem, here we introduce an interval estimate as an additional measure, namely prediction interval (PI), which can be estimated from the error distribution of the predictions. The benefits of using the interval estimate are 1) it provides the uncertainty range in the predicted activities, which is important in prospective applications; 2) a true null model with well-defined PI can be established. We provide one such example termed Gaussian Random Affinity Model (GRAM), which is based on the empirical observation that the affinity change in a typical lead optimization effort has the tendency to distribute normally N (0, s). Having an analytically defined PI that only depends on the variation in the activities, GRAM should in principle allow us to compare the performance of relative binding affinity prediction methods in a standard way, ultimately critical to measuring the progress made in algorithm development.<br>

Improving the Accuracy of Protein-Ligand Binding Affinity Prediction by Deep Learning Models: Benchmark and Model

2019 ◽  
Author(s):  
Mohammad Rezaei ◽  
Yanjun Li ◽  
Xiaolin Li ◽  
Chenglong Li
Keyword(s):  
Deep Learning ◽  
Drug Design ◽  
Binding Affinity ◽  
Benchmark Dataset ◽  
Rational Drug Design ◽  
Learning Models ◽  
Structure Based Drug Design ◽  
Binding Affinity Prediction ◽  
Affinity Prediction ◽  
Rational Drug

<b>Introduction:</b> The ability to discriminate among ligands binding to the same protein target in terms of their relative binding affinity lies at the heart of structure-based drug design. Any improvement in the accuracy and reliability of binding affinity prediction methods decreases the discrepancy between experimental and computational results.<br><b>Objectives:</b> The primary objectives were to find the most relevant features affecting binding affinity prediction, least use of manual feature engineering, and improving the reliability of binding affinity prediction using efficient deep learning models by tuning the model hyperparameters.<br><b>Methods:</b> The binding site of target proteins was represented as a grid box around their bound ligand. Both binary and distance-dependent occupancies were examined for how an atom affects its neighbor voxels in this grid. A combination of different features including ANOLEA, ligand elements, and Arpeggio atom types were used to represent the input. An efficient convolutional neural network (CNN) architecture, DeepAtom, was developed, trained and tested on the PDBbind v2016 dataset. Additionally an extended benchmark dataset was compiled to train and evaluate the models.<br><b>Results: </b>The best DeepAtom model showed an improved accuracy in the binding affinity prediction on PDBbind core subset (Pearson’s R=0.83) and is better than the recent state-of-the-art models in this field. In addition when the DeepAtom model was trained on our proposed benchmark dataset, it yields higher correlation compared to the baseline which confirms the value of our model.<br><b>Conclusions:</b> The promising results for the predicted binding affinities is expected to pave the way for embedding deep learning models in virtual screening and rational drug design fields.

Role of polarization in ligand docking and binding affinity prediction for inhibitors of dengue virus

2011 ◽  
Vol 21 (7) ◽  
pp. 1030-1038 ◽  
Author(s):  
Kshatresh Dutta Dubey ◽  
Amit Kumar Chaubey ◽  
Rajendra Prasad Ojha
Keyword(s):  
Dengue Virus ◽  
Binding Affinity ◽  
Ligand Docking ◽  
Binding Affinity Prediction ◽  
Affinity Prediction
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