相扑蛋白
生物
乙酰化
泛素
转录因子
翻译后修饰
药物发现
细胞生物学
计算生物学
基因
遗传学
生物信息学
生物化学
酶
作者
Charles A. C. Williams,Abdenour Soufi,Steven M. Pollard
标识
DOI:10.1016/j.semcancer.2019.09.009
摘要
Sox proteins are a family of lineage-associated transcription factors. They regulate expression of genes involved in control of self-renewal and multipotency in both developmental and adult stem cells. Overexpression of Sox proteins is frequently observed in many different human cancers. Despite their importance as therapeutic targets, Sox proteins are difficult to 'drug' using structure-based design. However, Sox protein localisation, activity and interaction partners are regulated by a plethora of post-translational modifications (PTMs), such as: phosphorylation, acetylation, sumoylation, methylation, and ubiquitylation. Here we review the various reported post-translational modifications of Sox proteins and their potential functional importance in guiding cell fate processes. The enzymes that regulate these PTMs could be useful targets for anti-cancer drug discovery.
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