Literature DB >> 15178329

Functionally and structurally relevant residues of enzymes: are they segregated or overlapping?

Csaba Magyar1, Eva Tüdos, István Simon.   

Abstract

There is a delicate balance between stability and flexibility needed for enzyme function. To avoid undesirable alteration of the functional properties during the evolutionary optimization of the structural stability under certain circumstances, and vice versa, to avoid unwanted changes of stability during the optimization of the functional properties of proteins, common sense would suggest that parts of the protein structure responsible for stability and parts responsible for function developed and evolved separately. This study shows that nature did not follow this anthropomorphic logic: the set of residues involved in function and those involved in structural stabilization of enzymes are rather overlapping than segregated.

Mesh:

Substances:

Year:  2004        PMID: 15178329     DOI: 10.1016/j.febslet.2004.04.070

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


  3 in total

1.  Graph-representation of oxidative folding pathways.

Authors:  Vilmos Agoston; Masa Cemazar; László Kaján; Sándor Pongor
Journal:  BMC Bioinformatics       Date:  2005-01-27       Impact factor: 3.169

2.  Relationship between Metabolic Fluxes and Sequence-Derived Properties of Enzymes.

Authors:  Peteris Zikmanis; Inara Kampenusa
Journal:  Int Sch Res Notices       Date:  2014-10-29

3.  Relationships between kinetic constants and the amino acid composition of enzymes from the yeast Saccharomyces cerevisiae glycolysis pathway.

Authors:  Peteris Zikmanis; Inara Kampenusa
Journal:  EURASIP J Bioinform Syst Biol       Date:  2012-08-06
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.