4.5 Review

Redox properties of tyrosine and related molecules

期刊

FEBS LETTERS
卷 586, 期 5, 页码 596-602

出版社

WILEY
DOI: 10.1016/j.febslet.2011.12.014

关键词

Electron transfer; Tyrosine; Tyrosyl radical

资金

  1. NIH [DK019038, GM095037]

向作者/读者索取更多资源

Redox reactions of tyrosine play key roles in many biological processes, including water oxidation and DNA synthesis. We first review the redox properties of tyrosine (and other phenols) in small molecules and related polypeptides, then report work on (H20)/(Y48)-modified Pseudomonas aeruginosa azurin. The crystal structure of this protein (1.18 angstrom resolution) shows that H20 is strongly hydrogen bonded to Y48 (2.7-2.8 angstrom tyrosine-O to histidine-N distance). A firm conclusion is that proper tuning of the tyrosine potential by a proton-accepting base is critical for biological redox functions. (C) 2011 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