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Conservation of the separase regulatory domain

ᅟ: 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. Her...

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Detalles Bibliográficos
Autores principales: Melesse, Michael, Bembenek, Joshua N., Zhulin, Igor B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921967/
https://www.ncbi.nlm.nih.gov/pubmed/29703221
http://dx.doi.org/10.1186/s13062-018-0210-0
Descripción
Sumario:ᅟ: 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13062-018-0210-0) contains supplementary material, which is available to authorized users.