Tang Zhongshu, Hecker Christina M, Scheschonka Astrid, Betz Heinrich
Department of Neurochemistry, Max-Planck-Institute for Brain Research, Deutschordenstrasse 46, Frankfurt, Germany.
FEBS J. 2008 Jun;275(12):3003-15. doi: 10.1111/j.1742-4658.2008.06459.x. Epub 2008 May 17.
Sumoylation is a multi-step protein modification reaction in which SUMO (small ubiquitin-like modifier) proteins are covalently attached to lysine residues of substrate proteins. Here, we compare the sequences and structures of modifiers and enzymes involved in sumoylation with those of the related ubiquitination and neddylation cascades. By using available structural data on modifier/enzyme/substrate interactions, we discuss and model sumoylation complexes that include SUMO-1 and the E1 and E2 enzymes Aos1-uba2 and ubc9, or SUMO-1 and E2 together with the E3 ligase RanBP2 and its substrate RanGAP1. Their comparison provides insight into the protein interactions underlying sumoylation, and suggests how SUMO proteins may be translocated between enzymes during the various steps of the protein modification reaction.
SUMO化是一种多步骤的蛋白质修饰反应,其中SUMO(小泛素样修饰物)蛋白共价连接到底物蛋白的赖氨酸残基上。在这里,我们将SUMO化过程中涉及的修饰物和酶的序列及结构与相关的泛素化和NEDD化级联反应中的序列及结构进行比较。通过利用修饰物/酶/底物相互作用的现有结构数据,我们讨论并构建了包含SUMO-1以及E1和E2酶Aos1-Uba2和Ubc9的SUMO化复合物模型,或者包含SUMO-1和E2以及E3连接酶RanBP2及其底物RanGAP1的模型。它们之间的比较为SUMO化背后的蛋白质相互作用提供了见解,并表明在蛋白质修饰反应的各个步骤中SUMO蛋白可能如何在酶之间转移。