Literature DB >> 16600599

To be or not to be an oxidase: challenging the oxygen reactivity of flavoenzymes.

Andrea Mattevi1.   

Abstract

Flavin-dependent enzymes catalyse a wide range of reactions and, thereby, facilitate a variety of cellular processes. Among the properties that equip flavoenzymes with this chemical versatility is their reactivity towards oxygen, which shows huge variation among flavoproteins. A survey of known 3D structures of flavin-dependent oxidases and dehydrogenases and the correlation with their functional properties indicates that there are no structural rules that enable prediction of whether or how a flavoenzyme reacts with oxygen. Combinations of subtle factors such as dipole pre-organization, charge distribution, dynamics and solvation in the active centre determine the balance of interactions that control oxygen reactivity. The chemical basis of oxygen reactivity remains a puzzling problem and represents one of the challenging questions in modern flavoenzymology.

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Year:  2006        PMID: 16600599     DOI: 10.1016/j.tibs.2006.03.003

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


  83 in total

1.  Flavin-linked Erv-family sulfhydryl oxidases release superoxide anion during catalytic turnover.

Authors:  Vidyadhar N Daithankar; Wenzhong Wang; Joliene R Trujillo; Colin Thorpe
Journal:  Biochemistry       Date:  2011-12-16       Impact factor: 3.162

2.  Structural characterization of mutations at the oxygen activation site in monomeric sarcosine oxidase .

Authors:  Marilyn Schuman Jorns; Zhi-Wei Chen; F Scott Mathews
Journal:  Biochemistry       Date:  2010-05-04       Impact factor: 3.162

3.  Structure and mechanism of ORF36, an amino sugar oxidizing enzyme in everninomicin biosynthesis .

Authors:  Jessica L Vey; Ahmad Al-Mestarihi; Yunfeng Hu; Michael A Funk; Brian O Bachmann; T M Iverson
Journal:  Biochemistry       Date:  2010-11-02       Impact factor: 3.162

4.  Oxygen reactivity in flavoenzymes: context matters.

Authors:  Claudia A McDonald; Rebecca L Fagan; François Collard; Vincent M Monnier; Bruce A Palfey
Journal:  J Am Chem Soc       Date:  2011-10-04       Impact factor: 15.419

5.  Structure of the monooxygenase component of a two-component flavoprotein monooxygenase.

Authors:  Andrea Alfieri; Francesco Fersini; Nantidaporn Ruangchan; Methinee Prongjit; Pimchai Chaiyen; Andrea Mattevi
Journal:  Proc Natl Acad Sci U S A       Date:  2007-01-16       Impact factor: 11.205

6.  Aminoperoxide adducts expand the catalytic repertoire of flavin monooxygenases.

Authors:  Arne Matthews; Raspudin Saleem-Batcha; Jacob N Sanders; Frederick Stull; K N Houk; Robin Teufel
Journal:  Nat Chem Biol       Date:  2020-02-17       Impact factor: 15.040

Review 7.  Generating disulfides with the Quiescin-sulfhydryl oxidases.

Authors:  Erin J Heckler; Pumtiwitt C Rancy; Vamsi K Kodali; Colin Thorpe
Journal:  Biochim Biophys Acta       Date:  2007-10-12

8.  Ribulose 1,5-bisphosphate carboxylase/oxygenase activates O2 by electron transfer.

Authors:  Camille Bathellier; Li-Juan Yu; Graham D Farquhar; Michelle L Coote; George H Lorimer; Guillaume Tcherkez
Journal:  Proc Natl Acad Sci U S A       Date:  2020-09-15       Impact factor: 11.205

9.  A conserved active-site threonine is important for both sugar and flavin oxidations of pyranose 2-oxidase.

Authors:  Warintra Pitsawong; Jeerus Sucharitakul; Methinee Prongjit; Tien-Chye Tan; Oliver Spadiut; Dietmar Haltrich; Christina Divne; Pimchai Chaiyen
Journal:  J Biol Chem       Date:  2010-01-20       Impact factor: 5.157

10.  A threonine on the active site loop controls transition state formation in Escherichia coli respiratory complex II.

Authors:  Thomas M Tomasiak; Elena Maklashina; Gary Cecchini; Tina M Iverson
Journal:  J Biol Chem       Date:  2008-04-02       Impact factor: 5.157

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