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泛素介导的蛋白质水解:通过降解实现生物调控

Ubiquitin-mediated proteolysis: biological regulation via destruction.

作者信息

Ciechanover A, Orian A, Schwartz A L

机构信息

Department of Biochemistry, The Bruce Rappaport Faculty of Medicine and the Rappaport Family Institute for Research in the Medical Sciences, Technion-Israel Institute of Technology, Israel.

出版信息

Bioessays. 2000 May;22(5):442-51. doi: 10.1002/(SICI)1521-1878(200005)22:5<442::AID-BIES6>3.0.CO;2-Q.

Abstract

The ubiquitin proteolytic system plays an important role in a broad array of basic cellular processes. Among these are regulation of cell cycle, modulation of the immune and inflammatory responses, control of signal transduction pathways, development and differentiation. These complex processes are controlled via specific degradation of a single or a subset of proteins. Degradation of a protein by the ubiquitin system involves two successive steps, conjugation of multiple moieties of ubiquitin and degradation of the tagged protein by the 26S proteasome. An important question concerns the identity of the mechanisms that underlie the high degree of specificity of the system. Substrate recognition is governed by a large family ubiquitin ligases that recognize the substrates, bind them and catalyze/facilitate their interaction with ubiquitin.

摘要

泛素蛋白酶系统在广泛的基本细胞过程中发挥着重要作用。其中包括细胞周期调控、免疫和炎症反应调节、信号转导通路控制、发育和分化。这些复杂过程通过单个或一组蛋白质的特异性降解来控制。泛素系统对蛋白质的降解涉及两个连续步骤,即多个泛素部分的缀合以及被标记蛋白质被26S蛋白酶体降解。一个重要问题涉及该系统高度特异性背后的机制的身份。底物识别由一大类泛素连接酶控制,这些连接酶识别底物、结合它们并催化/促进它们与泛素的相互作用。

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