Figure 1 | Scientific Reports

Figure 1

From: Structural analysis of human SEPHS2 protein, a selenocysteine machinery component, over-expressed in triple negative breast cancer

Figure 1

Sequence analysis of human SEPHS2. The negatively and positively charged residues are shown in red and cyan, respectively. We report predictions for secondary structure (Jnet), disorder propensity (Meta_d and IUPred), globularity propensity (GlobPL), predicted and experimentally determined phosphorylation sites (NetPhos and Phosphosite), sulfination sites (Sulfinator), glycosylation sites (NetNGlyc and NetOGlyc), and molecular recognition features (MorfPred and ANCHOR).

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