Literature DB >> 15134932

Aberrant activity of the DNA repair enzyme AlkB.

Timothy F Henshaw1, Michael Feig, Robert P Hausinger.   

Abstract

Escherichia coli AlkB is a DNA/RNA repair enzyme containing a mononuclear Fe(II) site that couples the oxidative decomposition of alpha-ketoglutarate (alphaKG) to the hydroxylation of 1-methyladenine or 3-methylcytosine lesions in DNA or RNA, resulting in release of formaldehyde and restoration of the normal bases. In the presence of Fe(II), alphaKG, and oxygen, but the absence of methylated DNA, AlkB was found to catalyze an aberrant reaction that generates a blue chromophore. The color is proposed to derive from Fe(III) coordinated by a hydroxytryptophan at position 178 as revealed by mass spectrometric analysis. Protein structural modeling confirms that Trp 178 is reasonably positioned to react with the Fe(IV)-oxo intermediate proposed to form at the active site.

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Year:  2004        PMID: 15134932     DOI: 10.1016/j.jinorgbio.2003.10.021

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


  28 in total

1.  In vivo self-hydroxylation of an iron-substituted manganese-dependent extradiol cleaving catechol dioxygenase.

Authors:  Erik R Farquhar; Joseph P Emerson; Kevin D Koehntop; Mark F Reynolds; Milena Trmčić; Lawrence Que
Journal:  J Biol Inorg Chem       Date:  2011-01-30       Impact factor: 3.358

2.  Self-hydroxylation of taurine/alpha-ketoglutarate dioxygenase: evidence for more than one oxygen activation mechanism.

Authors:  Kevin D Koehntop; Sudha Marimanikkuppam; Matthew J Ryle; Robert P Hausinger; Lawrence Que
Journal:  J Biol Inorg Chem       Date:  2005-12-01       Impact factor: 3.358

Review 3.  Direct reversal of DNA alkylation damage.

Authors:  Yukiko Mishina; Erica M Duguid; Chuan He
Journal:  Chem Rev       Date:  2006-02       Impact factor: 60.622

Review 4.  Oxidative dealkylation DNA repair mediated by the mononuclear non-heme iron AlkB proteins.

Authors:  Yukiko Mishina; Chuan He
Journal:  J Inorg Biochem       Date:  2006-02-15       Impact factor: 4.155

5.  Coordination changes and auto-hydroxylation of FIH-1: uncoupled O2-activation in a human hypoxia sensor.

Authors:  Yuan-Han Chen; Lindsay M Comeaux; Robert W Herbst; Evren Saban; David C Kennedy; Michael J Maroney; Michael J Knapp
Journal:  J Inorg Biochem       Date:  2008-08-08       Impact factor: 4.155

6.  Uncoupled O2-activation in the human HIF-asparaginyl hydroxylase, FIH, does not produce reactive oxygen species.

Authors:  Evren Saban; Shannon C Flagg; Michael J Knapp
Journal:  J Inorg Biochem       Date:  2011-01-21       Impact factor: 4.155

7.  Fe(II)/alpha-ketoglutarate hydroxylases involved in nucleobase, nucleoside, nucleotide, and chromatin metabolism.

Authors:  Jana M Simmons; Tina A Müller; Robert P Hausinger
Journal:  Dalton Trans       Date:  2008-06-27       Impact factor: 4.390

8.  Evaluation of a concerted vs. sequential oxygen activation mechanism in α-ketoglutarate-dependent nonheme ferrous enzymes.

Authors:  Serra Goudarzi; Shyam R Iyer; Jeffrey T Babicz; James J Yan; Günther H J Peters; Hans E M Christensen; Britt Hedman; Keith O Hodgson; Edward I Solomon
Journal:  Proc Natl Acad Sci U S A       Date:  2020-02-24       Impact factor: 11.205

9.  Crystal structure of prolyl 4-hydroxylase from Bacillus anthracis.

Authors:  Megen A Culpepper; Emily E Scott; Julian Limburg
Journal:  Biochemistry       Date:  2010-01-12       Impact factor: 3.162

10.  Crystal structure of Tpa1 from Saccharomyces cerevisiae, a component of the messenger ribonucleoprotein complex.

Authors:  Hyoun Sook Kim; Hye Lee Kim; Kyoung Hoon Kim; Do Jin Kim; Sang Jae Lee; Ji Young Yoon; Hye Jin Yoon; Hyang Yeon Lee; Seung Bum Park; Soon-Jong Kim; Jae Young Lee; Se Won Suh
Journal:  Nucleic Acids Res       Date:  2009-12-29       Impact factor: 16.971

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