How do I get the most out of my protein sequence using bioinformatics tools?

Acta Crystallogr D Struct Biol. 2021 Sep 1;77(Pt 9):1116-1126. doi: 10.1107/S2059798321007907. Epub 2021 Aug 24.

Abstract

Biochemical and biophysical experiments are essential for uncovering the three-dimensional structure and biological role of a protein of interest. However, meaningful predictions can frequently also be made using bioinformatics resources that transfer knowledge from a well studied protein to an uncharacterized protein based on their evolutionary relatedness. These predictions are helpful in developing specific hypotheses to guide wet-laboratory experiments. Commonly used bioinformatics resources include methods to identify and predict conserved sequence motifs, protein domains, transmembrane segments, signal sequences, and secondary as well as tertiary structure. Here, several such methods available through the MPI Bioinformatics Toolkit (https://toolkit.tuebingen.mpg.de) are described and how their combined use can provide meaningful information on a protein of unknown function is demonstrated. In particular, the identification of homologs of known structure using HHpred, internal repeats using HHrepID, coiled coils using PCOILS and DeepCoil, and transmembrane segments using Quick2D are focused on.

Keywords: bioinformatics tools; coiled coils; deep homology searches; homology modeling; protein sequence annotation; sequence features.

MeSH terms

  • Computational Biology / methods*
  • Models, Molecular
  • Protein Conformation*
  • Proteins / chemistry*
  • Software*

Substances

  • Proteins

Grants and funding

This work was funded by Max-Planck-Gesellschaft.