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Related Concept Videos

Protein-protein Interfaces02:04

Protein-protein Interfaces

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Many proteins form complexes to carry out their functions, making protein-protein interactions (PPIs) essential for an organism's survival. Most PPIs are stabilized by numerous weak noncovalent chemical forces. The physical shape of the interfaces determines the way two proteins interact. Many globular proteins have closely-matching shapes on their surfaces, which form a large number of weak bonds. Additionally, many PPIs occur between two helices or between a surface cleft and a...
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An organism can have thousands of different proteins, and these proteins must cooperate to ensure the health of an organism. Proteins bind to other proteins and form complexes to carry out their functions. Many proteins interact with multiple other proteins creating a complex network of protein interactions.
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lncRNA - Long Non-coding RNAs02:39

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In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
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Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
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Related Experiment Videos

EnANNDeep: An Ensemble-based lncRNA-protein Interaction Prediction Framework with Adaptive k-Nearest Neighbor

Lihong Peng1,2, Jingwei Tan3, Xiongfei Tian3

  • 1School of Computer Science, Hunan University of Technology, Zhuzhou, China. plhhnu@163.com.

Interdisciplinary Sciences, Computational Life Sciences
|January 10, 2022
PubMed
Summary

This study introduces EnANNDeep, an ensemble learning framework for predicting long non-coding RNA-protein interactions (LPIs). EnANNDeep demonstrates superior prediction accuracy compared to existing models, enhancing biological process understanding.

Keywords:
Adaptive k-nearest neighborDeep forestDeep neural networkEnsemble learninglncRNA–protein interaction

Related Experiment Videos

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Long non-coding RNA-protein interactions (LPIs) are crucial for biological processes.
  • Existing computational methods for LPI prediction often suffer from dataset bias and limited validation strategies.
  • Current models fail to effectively predict interactions for novel lncRNAs or proteins.

Purpose of the Study:

  • To develop a robust computational framework, EnANNDeep, for accurate LPI prediction.
  • To address limitations of existing methods by employing rigorous cross-validation across lncRNAs, proteins, and pairs.
  • To systematically identify potential LPIs for a deeper understanding of molecular mechanisms.

Main Methods:

  • Integration of multiple feature sources to represent lncRNA-protein pairs.
  • Development of an ensemble learning framework combining adaptive k-nearest neighbor, deep neural network, and deep forest models.
  • Application of soft voting to combine prediction probabilities from individual models.

Main Results:

  • EnANNDeep achieved superior performance over five classical LPI prediction models across multiple cross-validation strategies.
  • The model demonstrated high average AUCs (0.8660-0.9166) and AUPRs (0.8545-0.9054).
  • Case study identified a potential dense linkage between SNHG10 and protein Q15717.

Conclusions:

  • EnANNDeep offers a powerful and reliable approach for LPI prediction, overcoming limitations of previous methods.
  • The adaptive k-nearest neighbor component allows for flexible parameter selection.
  • Deep learning components effectively capture essential features of lncRNAs and proteins for accurate interaction prediction.