Identification of divergent WH2 motifs by HMM-HMM alignments

BMC Res Notes. 2015 Jan 24:8:18. doi: 10.1186/s13104-015-0981-7.

Abstract

Background: The actin cytoskeleton is a hallmark of eukaryotic cells. Its regulation as well as its interaction with other proteins is carefully orchestrated by actin interaction domains. One of the key players is the WH2 motif, which enables binding to actin monomers and filaments and is involved in the regulation of actin nucleation. Contrasting conserved domains, the identification of this motif in protein sequences is challenging, as it is short and poorly conserved.

Findings: To identify divergent members, we combined Hidden-Markov-Model (HMM) to HMM alignments with orthology predictions. Thereby, we identified nearly 500 proteins containing so far not annotated WH2 motifs. This included shootin-1, an actin binding protein involved in neuron polarization. Among others, WH2 motifs of 'proximal to raf' (ptr)-orthologs, which are described in the literature, but not annotated in genome databases, were identified.

Conclusion: In summary, we increased the number of WH2 motif containing proteins substantially. This identification of candidate regions for actin interaction could steer their experimental characterization. Furthermore, the approach outlined here can easily be adapted to the identification of divergent members of further domain families.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / chemistry
  • Actin Cytoskeleton / metabolism
  • Actins / chemistry
  • Actins / metabolism*
  • Alveolata / chemistry
  • Alveolata / metabolism
  • Amino Acid Motifs
  • Amino Acid Sequence
  • Animals
  • Drosophila Proteins / chemistry*
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster / chemistry
  • Drosophila melanogaster / metabolism
  • Euglenozoa / chemistry
  • Euglenozoa / metabolism
  • Fungi / chemistry
  • Fungi / metabolism
  • Mice
  • Microfilament Proteins / chemistry*
  • Microfilament Proteins / metabolism
  • Molecular Sequence Data
  • Nerve Tissue Proteins / chemistry*
  • Nerve Tissue Proteins / metabolism
  • Protein Binding
  • Protein Interaction Domains and Motifs*
  • Sequence Alignment / methods
  • Sequence Alignment / statistics & numerical data*
  • Thymosin / analogs & derivatives*
  • Thymosin / chemistry
  • Thymosin / metabolism
  • Ubiquitins / chemistry*
  • Ubiquitins / metabolism

Substances

  • Actins
  • Drosophila Proteins
  • Microfilament Proteins
  • Nerve Tissue Proteins
  • Ubiquitins
  • shootin 1 protein, mouse
  • spir protein, Drosophila
  • thymosin beta(1)
  • Thymosin