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Following Ariadne's thread: a new perspective on RBR ubiquitin ligases

机译:遵循Ariadne的观点:RBR泛素连接酶的新观点

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Ubiquitin signaling pathways rely on E3 ligases for effecting the final transfer of ubiquitin from E2 ubiquitin conjugating enzymes to a protein target. Here we re-evaluate the hybrid RING/ HECT mechanism used by the E3 family RING-between-RINGs (RBRs) to transfer ubiquitin to substrates. We place RBRs into the context of current knowledge of HECT and RING E3s. Although not as abundant as the other types of E3s (there are only slightly more than a dozen RBR E3s in the human genome), RBRs are conserved in all eukaryotes and play important roles in biology. Re-evaluation of RBR ligases as RING/ HECT E3s provokes new questions and challenges the field.
机译:泛素信号传导途径依赖于E3连接酶来实现泛素从E2泛素结合酶到蛋白质靶标的最终转移。在这里,我们重新评估了E3族环间环(RBR)用来将泛素转移至底物的混合RING / HECT机制。我们将RBR置于HECT和RING E3的当前知识环境中。尽管不如其他类型的E3丰富(人类基因组中只有十几个RBR E3),但RBR在所有真核生物中都是保守的,并在生物学中起重要作用。随着RING / HECT E3的出现,对RBR连接酶的重新评估引发了新的问题,并对该领域提出了挑战。

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