Literature DB >> 1618296

On the catalytic mechanism of EcoRI and EcoRV. A detailed proposal based on biochemical results, structural data and molecular modelling.

A Jeltsch1, J Alves, G Maass, A Pingoud.   

Abstract

EcoRI and EcoRV have a very similar active site, as is apparent from a comparison of the structures of their respective protein-DNA complexes. Based on structural and mechanistic data, as well as detailed molecular modelling presented here, a mechanism for the DNA cleavage by these enzymes is suggested in which the attacking water molecule is activated by the phosphate group 3' to the scissile phosphodiester bond, and in which the leaving group is protonated by a water molecule associated with the essential cofactor, Mg2+. The mechanism proposed may also apply to other nucleases.

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Year:  1992        PMID: 1618296     DOI: 10.1016/0014-5793(92)80576-3

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  13 in total

Review 1.  Substrate-assisted catalysis: molecular basis and biological significance.

Authors:  W Dall'Acqua; P Carter
Journal:  Protein Sci       Date:  2000-01       Impact factor: 6.725

Review 2.  The structural basis of damaged DNA recognition and endonucleolytic cleavage for very short patch repair endonuclease.

Authors:  S E Tsutakawa; K Morikawa
Journal:  Nucleic Acids Res       Date:  2001-09-15       Impact factor: 16.971

3.  Two crystal forms of the restriction enzyme MspI-DNA complex show the same novel structure.

Authors:  Qian Steven Xu; Richard J Roberts; Hwai-Chen Guo
Journal:  Protein Sci       Date:  2005-10       Impact factor: 6.725

Review 4.  Structure and function of type II restriction endonucleases.

Authors:  A Pingoud; A Jeltsch
Journal:  Nucleic Acids Res       Date:  2001-09-15       Impact factor: 16.971

5.  The crystal structure of EcoRV endonuclease and of its complexes with cognate and non-cognate DNA fragments.

Authors:  F K Winkler; D W Banner; C Oefner; D Tsernoglou; R S Brown; S P Heathman; R K Bryan; P D Martin; K Petratos; K S Wilson
Journal:  EMBO J       Date:  1993-05       Impact factor: 11.598

6.  KpnI restriction endonuclease and methyltransferase exhibit contrasting mode of sequence recognition.

Authors:  Siddamadappa Chandrashekaran; U H Manjunatha; Valakunja Nagaraja
Journal:  Nucleic Acids Res       Date:  2004-06-10       Impact factor: 16.971

7.  Cleavage properties of an oligonucleotide containing a bridged internucleotide 5'-phosphorothioate RNA linkage.

Authors:  R G Kuimelis; L W McLaughlin
Journal:  Nucleic Acids Res       Date:  1995-12-11       Impact factor: 16.971

8.  Substrate-assisted catalysis in the cleavage of DNA by the EcoRI and EcoRV restriction enzymes.

Authors:  A Jeltsch; J Alves; H Wolfes; G Maass; A Pingoud
Journal:  Proc Natl Acad Sci U S A       Date:  1993-09-15       Impact factor: 11.205

9.  Metal ion-mediated substrate-assisted catalysis in type II restriction endonucleases.

Authors:  N C Horton; K J Newberry; J J Perona
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-10       Impact factor: 11.205

10.  Identification of catalytically relevant amino acids of the extracellular Serratia marcescens endonuclease by alignment-guided mutagenesis.

Authors:  P Friedhoff; O Gimadutdinow; A Pingoud
Journal:  Nucleic Acids Res       Date:  1994-08-25       Impact factor: 16.971

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