Literature DB >> 23933321

Crystal structure of the CueO mutants at Glu506, the key amino acid located in the proton transfer pathway for dioxygen reduction.

Hirofumi Komori1, Takao Kajikawa, Kunishige Kataoka, Yoshiki Higuchi, Takeshi Sakurai.   

Abstract

Glu506 involved in the hydrogen bond network leading from solvent waters to the trinuclear copper center in a multicopper oxidase, CueO plays a crucial role to transport protons in the four-electron reduction of dioxygen to water. We performed X-ray crystal structure analyses of the Glu506Ala and Glu506Ile mutants, showing the formation of a compensatory proton transport pathway with only water molecules and a disruption of the hydrogen bond network due to the bulky side chain, respectively. We discuss the efficiency of proton transport through the hydrogen bond network based on the present results and our previous modification of the proton transport pathway by the Glu506 to Gln mutation, which have allowed us to trap and characterize the reaction intermediates.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CueO; Hydrogen bond network; MCO; Multicopper oxidase; O(2)-reduction; Proton transfer; Site-directed mutagenesis; T1; T2; T3; TNC; X-ray crystal structure; multicopper oxidase; trinuclear copper center; type I; type II; type III

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Year:  2013        PMID: 23933321     DOI: 10.1016/j.bbrc.2013.07.121

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  3 in total

1.  Exogenous acetate ion reaches the type II copper centre in CueO through the water-excretion channel and potentially affects the enzymatic activity.

Authors:  Hirofumi Komori; Kunishige Kataoka; Sakiko Tanaka; Nana Matsuda; Yoshiki Higuchi; Takeshi Sakurai
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2016-06-22       Impact factor: 1.056

2.  Biochemical, spectroscopic and X-ray structural analysis of deuterated multicopper oxidase CueO prepared from a new expression construct for neutron crystallography.

Authors:  Mahfuza Akter; Chika Inoue; Hirofumi Komori; Nana Matsuda; Takeshi Sakurai; Kunishige Kataoka; Yoshiki Higuchi; Naoki Shibata
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2016-09-22       Impact factor: 1.056

Review 3.  Laccase engineering by rational and evolutionary design.

Authors:  Isabel Pardo; Susana Camarero
Journal:  Cell Mol Life Sci       Date:  2015-01-14       Impact factor: 9.261

  3 in total

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