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- W2486133097 abstract "Peptide inter-domain linkers are peptide segments covalently linking two adjacent domains within a protein. Linkers play a variety of structural and functional roles in naturally occurring proteins. In this work we analyze the sequence properties of the predicted linker regions of the bacterial transcriptional regulators belonging to the recently discovered MocR subfamily of the GntR regulators. Analyses were carried out on the MocR sequences taken from the phyla Actinobacteria, Firmicutes, Alpha-, Beta- and Gammaproteobacteria. The results suggest that MocR linkers display phylum-specific characteristics and unique features different from those already described for other classes of inter-domain linkers. They show an average length significantly higher: 31.8 ± 14.3 residues reaching a maximum of about 150 residues. Compositional propensities displayed general and phylum-specific trends. Pro is dominating in all linkers. Dyad propensity analysis indicate Pro–Pro as the most frequent amino acid pair in all linkers. Physicochemical properties of the linker regions were assessed using amino acid indices relative to different features: in general, MocR linkers are flexible, hydrophilic and display propensity for β-turn or coil conformations. Linker sequences are hypervariable: only similarities between MocR linkers from organisms related at the level of species or genus could be found with sequence searches. The results shed light on the properties of the linker regions of the new MocR subfamily of bacterial regulators and may provide knowledge-based rules for designing artificial linkers with desired properties." @default.
- W2486133097 created "2016-08-23" @default.
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- W2486133097 date "2016-12-01" @default.
- W2486133097 modified "2023-10-16" @default.
- W2486133097 title "Structural properties of the linkers connecting the N- and C- terminal domains in the MocR bacterial transcriptional regulators" @default.
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- W2486133097 doi "https://doi.org/10.1016/j.biopen.2016.07.002" @default.
- W2486133097 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5801912" @default.
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