Conservation of the separase regulatory domain

Michael Melesse, Joshua N. Bembenek, Igor B. Zhulin

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

We report a protein sequence analysis of the cell cycle regulatory protease, separase. The sequence and structural conservation of the C-terminal protease domain has long been recognized, whereas the N-terminal regulatory domain of separase was reported to lack detectable sequence similarity. Here we reveal significant sequence conservation of the separase regulatory domain and report a discovery of a cysteine motif (CxCxxC) conserved in major lineages of Metazoa including nematodes and vertebrates. This motif is found in a solvent exposed linker region connecting two TPR-like helical motifs. Mutation of this motif in Caenorhabditis elegans separase leads to a temperature sensitive hypomorphic protein. Conservation of this motif in organisms ranging from C. elegans to humans suggests its functional importance. Reviewers: This article was reviewed by Lakshminarayan Iyer and Michael Galperin.

Original languageEnglish
Article number7
JournalBiology Direct
Volume13
Issue number1
DOIs
StatePublished - Apr 27 2018
Externally publishedYes

Funding

This work was supported in part by National Institutes of Health grants GM114471 (to J.N.B.) and GM072295 (to I.B.Z.).

Keywords

  • Conservation
  • Cysteine motif
  • PSI-BLAST
  • Separase

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