Literature DB >> 9242901

Mechanistic aspects of enzymatic catalysis: lessons from comparison of RNA and protein enzymes.

G J Narlikar1, D Herschlag.   

Abstract

A classic approach in biology, both organismal and cellular, is to compare morphologies in order to glean structural and functional commonalities. The comparative approach has also proven valuable on a molecular level. For example, phylogenetic comparisons of RNA sequences have led to determination of conserved secondary and even tertiary structures, and comparisons of protein structures have led to classifications of families of protein folds. Here we take this approach in a mechanistic direction, comparing protein and RNA enzymes. The aim of comparing RNA and protein enzymes is to learn about fundamental physical and chemical principles of biological catalysis. The more recently discovered RNA enzymes, or ribozymes, provide a distinct perspective on long-standing questions of biological catalysis. The differences described in this review have taught us about the aspects of RNA and proteins that are distinct, whereas the common features have helped us to understand the aspects that are fundamental to biological catalysis. This has allowed the framework that was put forth by Jencks for protein catalysts over 20 years ago (1) to be extended to RNA enzymes, generalized, and strengthened.

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Year:  1997        PMID: 9242901     DOI: 10.1146/annurev.biochem.66.1.19

Source DB:  PubMed          Journal:  Annu Rev Biochem        ISSN: 0066-4154            Impact factor:   23.643


  53 in total

1.  Helix P4 is a divalent metal ion binding site in the conserved core of the ribonuclease P ribozyme.

Authors:  E L Christian; N M Kaye; M E Harris
Journal:  RNA       Date:  2000-04       Impact factor: 4.942

2.  Involvement of a cytosine side chain in proton transfer in the rate-determining step of ribozyme self-cleavage.

Authors:  I H Shih ; M D Been
Journal:  Proc Natl Acad Sci U S A       Date:  2001-02-13       Impact factor: 11.205

3.  Evidence for a polynuclear metal ion binding site in the catalytic domain of ribonuclease P RNA.

Authors:  Eric L Christian; Nicholas M Kaye; Michael E Harris
Journal:  EMBO J       Date:  2002-05-01       Impact factor: 11.598

4.  Comparison of the hammerhead cleavage reactions stimulated by monovalent and divalent cations.

Authors:  J L O'Rear; S Wang; A L Feig; L Beigelman; O C Uhlenbeck; D Herschlag
Journal:  RNA       Date:  2001-04       Impact factor: 4.942

5.  Refolding of rRNA exons enhances dissociation of the Tetrahymena intron.

Authors:  Y Cao; S A Woodson
Journal:  RNA       Date:  2000-09       Impact factor: 4.942

6.  Dissection of a metal-ion-mediated conformational change in Tetrahymena ribozyme catalysis.

Authors:  Shu-ou Shan; Daniel Herschlag
Journal:  RNA       Date:  2002-07       Impact factor: 4.942

7.  Recognition of the 5' leader of pre-tRNA substrates by the active site of ribonuclease P.

Authors:  Nathan H Zahler; Eric L Christian; Michael E Harris
Journal:  RNA       Date:  2003-06       Impact factor: 4.942

8.  Exceptionally fast self-cleavage by a Neurospora Varkud satellite ribozyme.

Authors:  Ricardo Zamel; Alan Poon; Dominic Jaikaran; Angela Andersen; Joan Olive; Diane De Abreu; Richard A Collins
Journal:  Proc Natl Acad Sci U S A       Date:  2004-01-30       Impact factor: 11.205

9.  Characterization of the catalytic activity of U2 and U6 snRNAs.

Authors:  Saba Valadkhan; James L Manley
Journal:  RNA       Date:  2003-07       Impact factor: 4.942

10.  Specific phosphorothioate substitutions probe the active site of Bacillus subtilis ribonuclease P.

Authors:  Sharon M Crary; Jeffrey C Kurz; Carol A Fierke
Journal:  RNA       Date:  2002-07       Impact factor: 4.942

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