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.).

FundersFunder number
National Institutes of HealthGM072295
National Institute of General Medical SciencesR01GM114471

    Keywords

    • Conservation
    • Cysteine motif
    • PSI-BLAST
    • Separase

    Fingerprint

    Dive into the research topics of 'Conservation of the separase regulatory domain'. Together they form a unique fingerprint.

    Cite this