ELIOT: A platform to navigate the E3 pocketome and aid the design of new PROTACs

泛素连接酶 DNA连接酶 计算生物学 泛素 蛋白酶体 泛素蛋白连接酶类 生物 生物信息学 计算机科学 细胞生物学 遗传学 DNA 基因
作者
Tommaso Palomba,Massimo Baroni,Simon Cross,Gabriele Cruciani,Lydia Siragusa
出处
期刊:Chemical Biology & Drug Design [Wiley]
卷期号:101 (1): 69-86 被引量:7
标识
DOI:10.1111/cbdd.14123
摘要

Proteolysis-targeting chimeras (PROTACs) are novel therapeutics for the treatment of human disease. They exploit the enormous potential of the E3 ligases, a class of proteins that mark a target protein for degradation via the ubiquitin-proteasome system. Despite the existence of several E3 ligase-related databases, the choice of the functioning ligase is limited to only 1.6% of those available, probably due to the fragmentary understanding of their structures and their known ligands; in fact, none of the existing databases report detailed studies covering their 3D structure or their pockets. Here, we report ELIOT (E3 LIgase pocketOme navigaTor), an accurate and complete platform containing the E3 ligase pocketome to enable navigation and selection of new E3 ligases and new ligands for the design of new PROTACs. All E3 ligase pockets were characterized with innovative 3D descriptors including their PROTAC-ability score, and similarity analyses between E3 pockets are presented. Tissue specificity and their degree of involvement in patients with specific cancer types are also annotated for each E3 ligase, enabling appropriate selection for the design of a PROTAC with improved specificity. All data are available at https://eliot.moldiscovery.com.
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