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激活泛素家族:UBA6给该领域带来了挑战。

Activating the ubiquitin family: UBA6 challenges the field.

作者信息

Groettrup Marcus, Pelzer Christiane, Schmidtke Gunter, Hofmann Kay

机构信息

Division of Immunology, Department of Biology, University of Constance, D-78457 Konstanz, Germany.

出版信息

Trends Biochem Sci. 2008 May;33(5):230-7. doi: 10.1016/j.tibs.2008.01.005. Epub 2008 Mar 18.

Abstract

Since its discovery in 1981, ubiquitin-activating enzyme 1 was thought to be the only E1-type enzyme responsible for ubiquitin activation. Recently, a relatively uncharacterized E1 enzyme, designated ubiquitin-like modifier activating enzyme 6, was also shown to activate ubiquitin. Ubiquitin-activating enzyme 1 and ubiquitin-like modifier activating enzyme 6 are both essential proteins, and each uses a different spectrum of ubiquitin-conjugating (E2) enzymes. Ubiquitin-like modifier activating enzyme 6 activates not only ubiquitin, but also the ubiquitin-like modifier FAT10 (human leukocyte antigen F-associated transcript 10), which, similarly to ubiquitin, serves as a signal for proteasomal degradation. This new layer of regulation in ubiquitin activation markedly increases the versatility of the ubiquitin conjugation system.

摘要

自1981年被发现以来,泛素激活酶1一直被认为是唯一负责泛素激活的E1型酶。最近,一种相对未被充分表征的E1酶,即泛素样修饰物激活酶6,也被证明能够激活泛素。泛素激活酶1和泛素样修饰物激活酶6都是必需蛋白,并且各自使用不同的泛素缀合(E2)酶谱。泛素样修饰物激活酶6不仅能激活泛素,还能激活泛素样修饰物FAT10(人类白细胞抗原F相关转录本10),与泛素类似,FAT10也作为蛋白酶体降解的信号。泛素激活中这一新的调控层面显著增加了泛素缀合系统的多功能性。

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