The effect of methoxy group rotation and hydrogen bonding on the redox properties of ubiquinone
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry
Reference14 articles.
1. Photosystem II: the light-driven water: plastoquinone oxidoreductase;Rutherford;Trends Biochem. Sci.,2001
2. Structure of photosystem I;Fromme;Biochim. Biophys. Acta,2001
3. Protein−cofactor interactions and EPR parameters for the QH quinone binding site of quinol oxidase. A density functional study;Kacprzak;J. Am. Chem. Soc.,2006
4. Conformational differences between the methoxy groups of Q∼A and Q∼B site ubisemiquinones in bacterial reaction centers: a key role for methoxy group orientation in modulating ubiquinone redox potential;Taguchi;Biochemistry,2013
5. Tuning cofactor redox potentials: the 2-methoxy dihedral angle generates a redox potential difference greater than 160mV between the primary (QA) and secondary (QB) quinones of the photosynthetic reaction center;Taguchi;Biochemistry,2013
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3. Systematic High-Accuracy Prediction of Electron Affinities for Biological Quinones;Journal of Computational Chemistry;2018-10-03
4. Conformational control of cofactors in nature: The effect of methoxy group orientation on the electronic structure of ubisemiquinone;Chemical Physics Letters;2018-03
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