S100A7/Ran-binding protein 9 coevolution in mammals

被引:0
作者
Fabio D’Amico
Francesca Nadalin
Massimo Libra
机构
[1] University of Catania,Department of Biomedical and Biotechnological Sciences
[2] Sorbonne Université,Laboratoire de Biologie Computationnelle et Quantitative (LCQB)
来源
Immunogenetics | 2020年 / 72卷
关键词
Coevolution; S100A7; RanBP9; Mammals;
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学科分类号
摘要
S100A7 has been suggested to interact with Ran-binding protein 9. Both proteins are nowadays considered key effectors in immune response. Functional interaction between proteins is ensured by coevolution. The mechanisms of vertebrate coevolution between S100A7 and RanBP9 remain unclear. Several approaches for studying coevolution have been developed. Protein coevolution was inferred by calculating the linear correlation coefficients between inter-protein distance matrices using Mirrortree. We found an overall moderate correlation value (R = 0.53, p < 1e-06). Moreover, owing to the high conservation of RanBP9 protein among vertebrates, we chose to utilize a recent version of Blocks in Sequences (BIS2) algorithm implemented in BIS2Analyzer webserver. A coevolution cluster was identified between the two proteins (p < 8.10e-05). In conclusion, our coevolutionary analysis suggests that amino acid variations may modulate S100A7/RanBP9 interaction with potential pathogenic effects. Such findings could guide further analysis to better elucidate the function of S100A7 and RanBP9 and to design drugs targeting for these molecules in diseases.
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页码:155 / 164
页数:9
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