Year: 2017
Type: dissertation
Abstract: Short linear motifs (SLiMs) are regulatory binding sites that are involved in signalling and protein regulation. SLiMs are often found in intrinsically disordered regions (IDRs) which are rapidly evolving and lack stable tertiary conformations. Despite their prevalence throughout the proteome, many SLiMs still remain unknown and understanding how they cooperate and evolved are ongoing endeavours. The goal of this thesis is to address the properties of SLiMs and how they evolved, using bioinformatics methods and evolutionary models. To further examine the role of SLiMs in signal transduction, I show that deletion of predicted SLiMs (pSLiMs) has a broad range of quantitative effects on signalling pathway output. Next, to explore what properties are important in substrate recognition, I show that the combination and order of motifs can predict target specificity. Lastly, using a comparative phylogenetic approach to investigate the evolution of motifs, I provide evidence that phosphorylation and docking sites coevolved.
Source: TSpace (University of Toronto)
Author: Mitchell Li Cheong Man
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W2767254872