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The Met99Gln mutant of amicyanin from Paracoccus versutus

Lookup NU author(s): Professor Christopher Dennison

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Abstract

The axial copper ligand methionine has been replaced by a glutamine in the cupredoxin amicyanin from Paracoccus versutus. Dynamic and structural characteristics of the mutant have been studied in detail using UV/Vis, EPR, NMR, cyclic voltammetry, and isomorphous metal replacement. M99Q amicyanin is a blue copper protein with significant spectral and structural similarities to the other cupredoxins umecyanin, stellacyanin, and M121Q azurin. In addition, the functional properties of M99Q amicyanin, as reflected in the electron self-exchange rate constant and midpoint potential (165 mV), have been assessed and compared to values for M121Q azurin. For the latter protein, the published midpoint potential was corrected to the much lower value of 147 mV at pH 7, I = 0.1 M. These values are very similar to the midpoint potential of stellacyanin, which naturally possesses an axial glutamine ligand and has the lowest reduction potential for a naturally occurring cupredoxin. A remarkable feature of M99Q amicyanin, in the reduced state, is the relatively high pK(a)* value of 7.1 for its His96 ligand.


Publication metadata

Author(s): Diederix REM, Canters GW, Dennison C

Publication type: Article

Publication status: Published

Journal: Biochemistry

Year: 2000

Volume: 39

Issue: 31

Pages: 9551-9560

ISSN (print): 0006-2960

ISSN (electronic): 1943-295X

Publisher: American Chemical Society

URL: http://dx.doi.org/10.1021/bi000648o

DOI: 10.1021/bi000648o


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