ADVERTISEMENT

If you are seeing this message, you may be experiencing temporary network problems. Please wait a few minutes and refresh the page. If the problem persists, you may wish to report it to your local Network Manager.

It is also possible that your web browser is not configured or not able to display style sheets. In this case, although the visual presentation will be degraded, the site should continue to be functional. We recommend using the latest version of Microsoft or Mozilla web browser to help minimise these problems.

Wiley InterScience

< Previous Abstract  |  Next Abstract >

Save Article to My Profile      Download Citation      Request Permissions

Abstract |  References  |  Full Text: HTML, PDF (Size: 605K)  | Related Articles | Citation Tracking

MicroReview
House cleaning, a part of good housekeeping
Michael Y. Galperin 1 *, Olga V. Moroz 2 , Keith S. Wilson 2 and Alexey G. Murzin 3 *
  1 National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20894, USA.
  2 York Structural Biology Laboratory, Department of Chemistry, University of York, Heslington, York YO10 5YW, UK.
  3 MRC Centre for Protein Engineering, Hills Road, Cambridge CB2 2QH, UK.
Correspondence to   *E-mail galperin@ncbi.nlm.nih.gov; Tel. (+1) 301 435 5910; Fax (+1) 301 435 7794. E-mail agm@mrc-lmb.cam.ac.uk; Tel. (+44) 1223 402132; Fax (+44) 1223 402140.
Copyright 2005 Blackwell Publishing Ltd; No claim to original US government works

ABSTRACT

Cellular metabolism constantly generates by-products that are wasteful or even harmful. Such compounds are excreted from the cell or are removed through hydrolysis to normal cellular metabolites by various 'house-cleaning' enzymes. Some of the most important contaminants are non-canonical nucleoside triphosphates (NTPs) whose incorporation into the nascent DNA leads to increased mutagenesis and DNA damage. Enzymes intercepting abnormal NTPs from incorporation by DNA polymerases work in parallel with DNA repair enzymes that remove lesions produced by modified nucleotides. House-cleaning NTP pyrophosphatases targeting non-canonical NTPs belong to at least four structural superfamilies: MutT-related (Nudix) hydrolases, dUTPase, ITPase (Maf/HAM1) and all-α NTP pyrophosphatases (MazG). These enzymes have high affinity (Km's in the micromolar range) for their natural substrates (8-oxo-dGTP, dUTP, dITP, 2-oxo-dATP), which allows them to select these substrates from a mixture containing a ∼1000-fold excess of canonical NTPs. To date, many house-cleaning NTPases have been identified only on the basis of their side activity towards canonical NTPs and NDP derivatives. Integration of growing structural and biochemical data on these superfamilies suggests that their new family members cleanse the nucleotide pool of the products of oxidative damage and inappropriate methylation. House-cleaning enzymes, such as 6-phosphogluconolactonase, are also part of normal intermediary metabolism. Genomic data suggest that house-cleaning systems are more abundant than previously thought and include numerous analogous enzymes with overlapping functions. We discuss the structural diversity of these enzymes, their phylogenetic distribution, substrate specificity and the problem of identifying their true substrates.


Accepted 7 October, 2005.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1365-2958.2005.04950.x About DOI

Related Articles

  • Find other articles like this in Wiley InterScience
  • Find articles in Wiley InterScience written by any of the authors

Wiley InterScience is a member of CrossRef.

Cross Ref Member


Sign up here
Click here to go to the conference website
Currentprotocols.com
Now Available

Read this Virtual Issue from Traffic:

Microbiology

Virtual Issue

Read more at http://www.traffic.dk/

Special Issue
Click here to read the Special Issue
E-mail alerts
Sign up for e-alerts