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 language | English |
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Article number | 7 |
Journal | Biology Direct |
Volume | 13 |
Issue number | 1 |
DOIs | |
State | Published - Apr 27 2018 |
Externally published | Yes |
Funding
This work was supported in part by National Institutes of Health grants GM114471 (to J.N.B.) and GM072295 (to I.B.Z.).
Funders | Funder number |
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National Institutes of Health | GM072295 |
National Institute of General Medical Sciences | R01GM114471 |
Keywords
- Conservation
- Cysteine motif
- PSI-BLAST
- Separase