Literature DB >> 26315426

BIOPHYSICS. Comment on "Extreme electric fields power catalysis in the active site of ketosteroid isomerase".

Aditya Natarajan1, Filip Yabukarski1, Vandana Lamba1, Jason P Schwans2, Fanny Sunden1, Daniel Herschlag3.   

Abstract

Fried et al. (Reports, 19 December 2014, p. 1510) demonstrated a strong correlation between reaction rate and the carbonyl stretching frequency of a product analog bound to ketosteroid isomerase oxyanion hole mutants and concluded that the active-site electric field provides 70% of catalysis. Alternative comparisons suggest a smaller contribution, relative to the corresponding solution reaction, and highlight the importance of atomic-level descriptions.
Copyright © 2015, American Association for the Advancement of Science.

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Year:  2015        PMID: 26315426     DOI: 10.1126/science.aab1584

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  3 in total

1.  BIOPHYSICS. Response to Comments on "Extreme electric fields power catalysis in the active site of ketosteroid isomerase".

Authors:  Stephen D Fried; Steven G Boxer
Journal:  Science       Date:  2015-08-27       Impact factor: 47.728

2.  Regulation and Plasticity of Catalysis in Enzymes: Insights from Analysis of Mechanochemical Coupling in Myosin.

Authors:  Xiya Lu; Victor Ovchinnikov; Darren Demapan; Daniel Roston; Qiang Cui
Journal:  Biochemistry       Date:  2017-03-01       Impact factor: 3.162

3.  A Preorganized Electric Field Leads to Minimal Geometrical Reorientation in the Catalytic Reaction of Ketosteroid Isomerase.

Authors:  Yufan Wu; Stephen D Fried; Steven G Boxer
Journal:  J Am Chem Soc       Date:  2020-05-19       Impact factor: 15.419

  3 in total

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