Literature DB >> 22658756

Inner- and outer-sphere metal coordination in blue copper proteins.

Jeffrey J Warren1, Kyle M Lancaster, John H Richards, Harry B Gray.   

Abstract

Blue copper proteins (BCPs) comprise classic cases of Nature's profound control over the electronic structures and chemical reactivity of transition metal ions. Early studies of BCPs focused on their inner coordination spheres, that is, residues that directly coordinate Cu. Equally important are the electronic and geometric perturbations to these ligands provided by the outer coordination sphere. In this tribute to Hans Freeman, we review investigations that have advanced the understanding of how inner-sphere and outer-sphere coordination affects biological Cu properties.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22658756      PMCID: PMC3434318          DOI: 10.1016/j.jinorgbio.2012.05.002

Source DB:  PubMed          Journal:  J Inorg Biochem        ISSN: 0162-0134            Impact factor:   4.155


  82 in total

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Journal:  Nucleic Acids Res       Date:  2000-01-01       Impact factor: 16.971

2.  Letter: Redox properties of copper-thiaether complexes. Comparison to blue copper protein behavior.

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Journal:  J Am Chem Soc       Date:  1976-07-07       Impact factor: 15.419

3.  Structural basis of the ferrous iron specificity of the yeast ferroxidase, Fet3p.

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Journal:  Biochemistry       Date:  2006-10-24       Impact factor: 3.162

4.  Metalloenzymes: the entatic nature of their active sites.

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Journal:  Proc Natl Acad Sci U S A       Date:  1968-02       Impact factor: 11.205

5.  Electron transfer reactivity of type zero Pseudomonas aeruginosa azurin.

Authors:  Kyle M Lancaster; Ole Farver; Scot Wherland; Edward J Crane; John H Richards; Israel Pecht; Harry B Gray
Journal:  J Am Chem Soc       Date:  2011-03-15       Impact factor: 15.419

Review 6.  An outer-sphere hydrogen-bond network constrains copper coordination in blue proteins.

Authors:  Michael C Machczynski; Harry B Gray; John H Richards
Journal:  J Inorg Biochem       Date:  2002-02       Impact factor: 4.155

7.  UV Raman monitoring of histidine protonation and H-(2)H exchange in plastocyanin.

Authors:  Qiang Wu; Fangbiao Li; Weixun Wang; Michael H Hecht; Thomas G Spiro
Journal:  J Inorg Biochem       Date:  2002-02       Impact factor: 4.155

Review 8.  Rack-induced bonding in blue-copper proteins.

Authors:  B G Malmström
Journal:  Eur J Biochem       Date:  1994-08-01

9.  The introduction of a negative charge into the hydrophobic patch of Pseudomonas aeruginosa azurin affects the electron self-exchange rate and the electrochemistry.

Authors:  G Van Pouderoyen; S Mazumdar; N I Hunt; A O Hill; G W Canters
Journal:  Eur J Biochem       Date:  1994-06-01

10.  Resonance Raman spectroscopy of the azurin His117Gly mutant. Interconversion of type 1 and type 2 copper sites through exogenous ligands.

Authors:  T den Blaauwen; C W Hoitink; G W Canters; J Han; T M Loehr; J Sanders-Loehr
Journal:  Biochemistry       Date:  1993-11-23       Impact factor: 3.162

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  23 in total

1.  Design of a single protein that spans the entire 2-V range of physiological redox potentials.

Authors:  Parisa Hosseinzadeh; Nicholas M Marshall; Kelly N Chacón; Yang Yu; Mark J Nilges; Siu Yee New; Stoyan A Tashkov; Ninian J Blackburn; Yi Lu
Journal:  Proc Natl Acad Sci U S A       Date:  2015-12-02       Impact factor: 11.205

2.  A single protein redox ruler.

Authors:  Rajneesh K Bains; Jeffrey J Warren
Journal:  Proc Natl Acad Sci U S A       Date:  2015-12-16       Impact factor: 11.205

3.  Copper Oxidation/Reduction in Water and Protein: Studies with DFTB3/MM and VALBOND Molecular Dynamics Simulations.

Authors:  Haiyun Jin; Puja Goyal; Akshaya Kumar Das; Michael Gaus; Markus Meuwly; Qiang Cui
Journal:  J Phys Chem B       Date:  2015-12-17       Impact factor: 2.991

4.  Effect of circular permutation on the structure and function of type 1 blue copper center in azurin.

Authors:  Yang Yu; Igor D Petrik; Kelly N Chacón; Parisa Hosseinzadeh; Honghui Chen; Ninian J Blackburn; Yi Lu
Journal:  Protein Sci       Date:  2016-11-04       Impact factor: 6.725

5.  9, 10-Bis(8-Quinolinoxymethyl)Anthracene--A Fluorescent Sensor for Nanomolar Detection of Cu(2+) with Unusual Acid Stability of Cu(2+)-Complex.

Authors:  Prabhpreet Singh; Rahul Kumar; Subodh Kumar
Journal:  J Fluoresc       Date:  2013-10-11       Impact factor: 2.217

6.  Molecular dynamics simulations of apocupredoxins: insights into the formation and stabilization of copper sites under entatic control.

Authors:  Luciano A Abriata; Alejandro J Vila; Matteo Dal Peraro
Journal:  J Biol Inorg Chem       Date:  2014-01-30       Impact factor: 3.358

Review 7.  Metalloproteins containing cytochrome, iron-sulfur, or copper redox centers.

Authors:  Jing Liu; Saumen Chakraborty; Parisa Hosseinzadeh; Yang Yu; Shiliang Tian; Igor Petrik; Ambika Bhagi; Yi Lu
Journal:  Chem Rev       Date:  2014-04-23       Impact factor: 60.622

8.  Site-Specific 1D and 2D IR Spectroscopy to Characterize the Conformations and Dynamics of Protein Molecular Recognition.

Authors:  Sashary Ramos; Megan C Thielges
Journal:  J Phys Chem B       Date:  2019-03-21       Impact factor: 2.991

9.  Relaxation of structural constraints during Amicyanin unfolding.

Authors:  John J Kozak; Harry B Gray; Roberto A Garza-López
Journal:  J Inorg Biochem       Date:  2017-11-22       Impact factor: 4.155

10.  Revisiting dithiadiaza macrocyclic chelators for copper-64 PET imaging.

Authors:  Sergey Shuvaev; Elizaveta A Suturina; Nicholas J Rotile; Andrei Astashkin; Christopher J Ziegler; Alana W Ross; Tia L Walker; Peter Caravan; Ian S Taschner
Journal:  Dalton Trans       Date:  2020-10-20       Impact factor: 4.390

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