生物
简编
泛素连接酶
遗传学
泛素蛋白连接酶类
DNA连接酶
计算生物学
进化生物学
dna连接酶
DNA转座因子
DNA
基序列
生物信息学
基因组
作者
Ngee Kiat Chua,Tania J. González-Robles,Cameron J. Reddington,Jane Dudley-Fraser,Richard W. Birkinshaw,Jiru Han,Ashleigh Solano,Soon Wei Wong,Tomasz Kochańczyk,Joshua Peter,Mark A. Nakasone,Florian Aust,Jacob E. Munro,Yeh Huei Tong,Julie Iskander,Waruni Abeysekera,Alex Garnham,Hannah Huckstep,Matthew E. Ritchie,Ingrid E. Wertz
出处
期刊:Cell
[Cell Press]
日期:2026-03-20
卷期号:189 (7): 2167-2188.e27
被引量:7
标识
DOI:10.1016/j.cell.2026.01.029
摘要
To define and systematically characterize the human E3 ubiquitin ligase (E3) landscape, we generated the E3-ome, a compendium of E3s encoded by the human genome. The E3-ome integrates experimental data, bioinformatics, and published research, revealing 672 high-confidence E3s. We standardized E3 classifications to create a unified framework for annotation and comparative analysis. The E3-ome identified several previously unrecognized domains, motifs, E3 candidates, and relationships, expanding the diversity of E3s. Furthermore, the E3-ome mapped the spatial and physiological organization of E3s across human tissues and cell types, revealing context-dependent E3s. Genetic analyses identified disease-associated variants across the E3-ome, linking E3s to diverse human pathologies. Together, these analyses define the human E3 landscape at high resolution and deliver a foundational resource to drive mechanistic and therapeutic discovery.
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