In Silico Tools and Approaches for the Prediction of Functional and Structural Effects of Single-Nucleotide Polymorphisms on Proteins: An Expert Review

OMICS. 2021 Jan;25(1):23-37. doi: 10.1089/omi.2020.0141. Epub 2020 Oct 15.

Abstract

Single-nucleotide polymorphisms (SNPs) are single-base variants that contribute to human biological variation and pathogenesis of many human diseases. Among all SNP types, nonsynonymous single-nucleotide polymorphisms (nsSNPs) can alter many structural, biochemical, and functional features of a protein such as folding characteristics, charge distribution, stability, dynamics, and interactions with other proteins/nucleotides. These modifications in the protein structure can lead nsSNPs to be closely associated with many multifactorial diseases such as cancer, diabetes, and neurodegenerative diseases. Predicting structural and functional effects of nsSNPs with experimental approaches can be time-consuming and costly; hence, computational prediction tools and algorithms are being widely and increasingly utilized in biology and medical research. This expert review examines the in silico tools and algorithms for the prediction of functional or structural effects of SNP variants, in addition to the description of the phenotypic effects of nsSNPs on protein structure, association between pathogenicity of variants, and functional or structural features of disease-associated variants. Finally, case studies investigating the functional and structural effects of nsSNPs on selected protein structures are highlighted. We conclude that creating a consistent workflow with a combination of in silico approaches or tools should be considered to increase the performance, accuracy, and precision of the biological and clinical predictions made in silico.

Keywords: SNP; bioinformatics; human genetic variation; in silico tools; nonsynonymous single-nucleotide polymorphisms; proteomics.

MeSH terms

  • Algorithms
  • Computational Biology / methods*
  • Disease Susceptibility
  • Humans
  • Models, Biological*
  • Models, Molecular*
  • Polymorphism, Single Nucleotide*
  • Proteins / chemistry*
  • Proteins / genetics*
  • Reproducibility of Results
  • Structure-Activity Relationship

Substances

  • Proteins