Understanding the functional difference between growth arrest-specific protein 6 and protein S: an evolutionary approachStuder, R. A., Opperdoes, F. R., Nicolaes, G. A. F., Mulder, A. B. & Mulder, R., Oct-2014, In : Open Biology. 4, 10, 11 p., 140121.
Research output: Contribution to journal › Article › Academic › peer-review
Although protein S (PROS1) and growth arrest-specific protein 6 (GAS6) proteins are homologous with a high degree of structural similarity, they are functionally different. The objectives of this study were to identify the evolutionary origins from which these functional differences arose. Bioinformatics methods were used to estimate the evolutionary divergence time and to detect the amino acid residues under functional divergence between GAS6 and PROS1. The properties of these residues were analysed in the light of their three-dimensional structures, such as their stability effects, the identification of electrostatic patches and the identification potential protein-protein interaction. The divergence between GAS6 and PROS1 probably occurred during the whole-genome duplications in vertebrates. A total of 78 amino acid sites were identified to be under functional divergence. One of these sites, Asn463, is involved in N-glycosylation in GAS6, but is mutated in PROS1, preventing this post-translational modification. Sites experiencing functional divergence tend to express a greater diversity of stabilizing/destabilizing effects than sites that do not experience such functional divergence. Three electrostatic patches in the LG1/LG2 domains were found to differ between GAS6 and PROS1. Finally, a surface responsible for protein-protein interactions was identified. These results may help researchers to analyse disease-causing mutations in the light of evolutionary and structural constraints, and link genetic pathology to clinical phenotypes.
|Number of pages||11|
|Publication status||Published - Oct-2014|
- protein S, growth arrest-specific protein 6, evolution, SYSTEMIC-LUPUS-ERYTHEMATOSUS, C4B-BINDING PROTEIN, BETA-CHAIN, POSITIVE SELECTION, COFACTOR FUNCTION, MAXIMUM-LIKELIHOOD, SEQUENCE EVOLUTION, SEVERE SEPSIS, BINDING-SITE, FACTOR VA