Proton-Coupled Electron Transfer and Redox-Active Tyrosines: Structure and Function of the Tyrosyl Radicals in Ribonucleotide Reductase and Photosystem II-Reference-Cited by-同舟云学术

Proton-Coupled Electron Transfer and Redox-Active Tyrosines: Structure and Function of the Tyrosyl Radicals in Ribonucleotide Reductase and Photosystem II

Published:2012-02-08 Issue:4 Volume:3 Page:543-554
ISSN:1948-7185
Container-title:The Journal of Physical Chemistry Letters
language:en
Short-container-title:J. Phys. Chem. Lett.

Author:

Barry Bridgette A.¹,Chen Jun¹,Keough James¹,Jenson David¹,Offenbacher Adam¹,Pagba Cynthia¹

Affiliation:

1. School of Chemistry and Biochemistry and the Petit Institute for Bioengineering and Biosciences, Georgia Institute of Technology, Atlanta, Georgia 30332, United States

Publisher

American Chemical Society (ACS)

Subject

General Materials Science,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jz2014117

Reference107 articles.

1. Ribonucleotide reductases: amazing and confusing.

2. Tyrosine radicals are involved in the photosynthetic oxygen-evolving system.

3. Isotopic labeling and EPR spectroscopy show that a tyrosine residue is the terminal electron donor, Z, in manganese-depleted photosystem II preparations

4. Prostaglandin H synthase: spectroscopic studies of the interaction with hydroperoxides and with indomethacin

5. A tyrosine-derived free radical in apogalactose oxidase.

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