4.5 Article

Carboxy terminal extended phytocystatins are bifunctional inhibitors of papain and legumain cysteine proteinases

期刊

FEBS LETTERS
卷 581, 期 16, 页码 2914-2918

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.febslet.2007.05.042

关键词

barley; cystatin; cysteine proteinase inhibitor; legumain; papain

向作者/读者索取更多资源

Plant legumains are cysteine proteinases putatively involved in processing endogenous proteins. Phytocystatins (Phy-Cys) have been described as plant inhibitors of papain-like cysteine proteinases. Some PhyCys contain a carboxy terminal extension with an amino acid motif (SNSL) similar to that involved in the inhibition of legumain-like proteins by human cystatins. The role of these carboxy terminal extended PhyCys as inhibitors of legumain-like cysteine proteinases is here shown by in vitro inhibition of human legumain and legumain-like activities from barley extracts. Moreover, site-directed mutagenesis has demonstrated that the asparagine of the SNSL motif is essential in this inhibition. We prove for first time the existence of legumain inhibitors in plants. (c) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据