Literature DB >> 10739241

Substrate-assisted catalysis: molecular basis and biological significance.

W Dall'Acqua1, P Carter.   

Abstract

Substrate-assisted catalysis (SAC) is the process by which a functional group in a substrate contributes to catalysis by an enzyme. SAC has been demonstrated for representatives of three major enzyme classes: serine proteases, GTPases, and type II restriction endonucleases, as well as lysozyme and hexose-1-phosphate uridylyltransferase. Moreover, structure-based predictions of SAC have been made for many additional enzymes. Examples of SAC include both naturally occurring enzymes such as type II restriction endonucleases as well as engineered enzymes including serine proteases. In the latter case, a functional group from a substrate can substitute for a catalytic residue replaced by site-directed mutagenesis. From a protein engineering perspective, SAC provides a strategy for drastically changing enzyme substrate specificity or even the reaction catalyzed. From a biological viewpoint, SAC contributes significantly to the activity of some enzymes and may represent a functional intermediate in the evolution of catalysis. This review focuses on advances in engineering enzyme specificity and activity by SAC, together with the biological significance of this phenomenon.

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Year:  2000        PMID: 10739241      PMCID: PMC2144443          DOI: 10.1110/ps.9.1.1

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


  79 in total

1.  The 2.2 A crystal structure of transducin-alpha complexed with GTP gamma S.

Authors:  J P Noel; H E Hamm; P B Sigler
Journal:  Nature       Date:  1993-12-16       Impact factor: 49.962

2.  Substrate phage: selection of protease substrates by monovalent phage display.

Authors:  D J Matthews; J A Wells
Journal:  Science       Date:  1993-05-21       Impact factor: 47.728

Review 3.  Function and regulation of ras.

Authors:  D R Lowy; B M Willumsen
Journal:  Annu Rev Biochem       Date:  1993       Impact factor: 23.643

4.  Modeling study on the cleavage step of the self-splicing reaction in group I introns.

Authors:  R F Setlik; R Garduno-Juarez; J I Manchester; M Shibata; R L Ornstein; R Rein
Journal:  J Biomol Struct Dyn       Date:  1993-06

5.  Mammalian Ras interacts directly with the serine/threonine kinase Raf.

Authors:  A B Vojtek; S M Hollenberg; J A Cooper
Journal:  Cell       Date:  1993-07-16       Impact factor: 41.582

6.  Rapid evolution of a protein in vitro by DNA shuffling.

Authors:  W P Stemmer
Journal:  Nature       Date:  1994-08-04       Impact factor: 49.962

7.  Crystal structure of Escherichia coli RNase HI in complex with Mg2+ at 2.8 A resolution: proof for a single Mg(2+)-binding site.

Authors:  K Katayanagi; M Okumura; K Morikawa
Journal:  Proteins       Date:  1993-12

8.  Structural basis for transfer RNA aminoacylation by Escherichia coli glutaminyl-tRNA synthetase.

Authors:  J J Perona; M A Rould; T A Steitz
Journal:  Biochemistry       Date:  1993-08-31       Impact factor: 3.162

9.  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

10.  The active site of yeast aspartyl-tRNA synthetase: structural and functional aspects of the aminoacylation reaction.

Authors:  J Cavarelli; G Eriani; B Rees; M Ruff; M Boeglin; A Mitschler; F Martin; J Gangloff; J C Thierry; D Moras
Journal:  EMBO J       Date:  1994-01-15       Impact factor: 11.598

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  34 in total

1.  The α-amino group of the threonine substrate as the general base during tRNA aminoacylation: a new version of substrate-assisted catalysis predicted by hybrid DFT.

Authors:  Wenjuan Huang; Eric A C Bushnell; Christopher S Francklyn; James W Gauld
Journal:  J Phys Chem A       Date:  2011-09-26       Impact factor: 2.781

2.  The importance of dynamics in substrate-assisted catalysis and specificity.

Authors:  Qin Xu; Haobo Guo; Alexander Wlodawer; Hong Guo
Journal:  J Am Chem Soc       Date:  2006-05-10       Impact factor: 15.419

3.  Conformational changes in the di-domain structure of Arabidopsis phosphoethanolamine methyltransferase leads to active-site formation.

Authors:  Soon Goo Lee; Joseph M Jez
Journal:  J Biol Chem       Date:  2017-10-30       Impact factor: 5.157

4.  Evolution of structure and mechanistic divergence in di-domain methyltransferases from nematode phosphocholine biosynthesis.

Authors:  Soon Goo Lee; Joseph M Jez
Journal:  Structure       Date:  2013-09-05       Impact factor: 5.006

5.  2'-O-methyl nucleotide modified DNA substrates influence the cleavage efficiencies of BamHI and BglII.

Authors:  Zhaoxue Tong; Bin Zhao; Guojie Zhao; Hong Shang; Yifu Guan
Journal:  J Biosci       Date:  2014-09       Impact factor: 1.826

6.  H662 is the linchpin of ATP hydrolysis in the nucleotide-binding domain of the ABC transporter HlyB.

Authors:  Jelena Zaitseva; Stefan Jenewein; Thorsten Jumpertz; I Barry Holland; Lutz Schmitt
Journal:  EMBO J       Date:  2005-05-12       Impact factor: 11.598

7.  A catalytic mechanism for D-Tyr-tRNATyr deacylase based on the crystal structure of Hemophilus influenzae HI0670.

Authors:  Kap Lim; Aleksandra Tempczyk; Nicklas Bonander; John Toedt; Andrew Howard; Edward Eisenstein; Osnat Herzberg
Journal:  J Biol Chem       Date:  2003-02-04       Impact factor: 5.157

Review 8.  Why nature really chose phosphate.

Authors:  Shina C L Kamerlin; Pankaz K Sharma; Ram B Prasad; Arieh Warshel
Journal:  Q Rev Biophys       Date:  2013-01-15       Impact factor: 5.318

Review 9.  The motor domains of ABC-transporters. What can structures tell us?

Authors:  Christine Oswald; I Barry Holland; Lutz Schmitt
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2006-03-16       Impact factor: 3.000

10.  Monitoring disappearance of monomers and generation of resistance to proteolysis during the formation of the activation domain of human procarboxypeptidase A2 (ADA2h) amyloid fibrils by matrix-assisted laser-desorption ionization-time-of-flight-MS.

Authors:  Josep Villanueva; Virtudes Villegas; Enrique Querol; Francesc X Avilés; Luis Serrano
Journal:  Biochem J       Date:  2003-09-01       Impact factor: 3.857

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