Unbound MEDLINE

Structural relationships among proteins with different global topologies and their implications for function annotation strategies. Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] Journal article

 
TitleStructural relationships among proteins with different global topologies and their implications for function annotation strategies.
Author(s)Petrey D, Fischer M, Honig B 
InstitutionHoward Hughes Medical Institute, Department of Biochemistry and Molecular Biophysics, Center for Computational Biology and Bioinformatics, Columbia University, 1130 St. Nicholas Avenue, Room 815, New York, NY 10032, USA.
SourceProc Natl Acad Sci U S A 2009 Oct 13; 106(41):17377-82.
AbstractIt has become increasingly apparent that geometric relationships often exist between regions of two proteins that have quite different global topologies or folds. In this article, we examine whether such relationships can be used to infer a functional connection between the two proteins in question. We find, by considering a number of examples involving metal and cation binding, sugar binding, and aromatic group binding, that geometrically similar protein fragments can share related functions, even if they have been classified as belonging to different folds and topologies. Thus, the use of classifications inevitably limits the number of functional inferences that can be obtained from the comparative analysis of protein structures. In contrast, the development of interactive computational tools that recognize the "continuous" nature of protein structure/function space, by increasing the number of potentially meaningful relationships that are considered, may offer a dramatic enhancement in the ability to extract information from protein structure databases. We introduce the MarkUs server, that embodies this strategy and that is designed for a user interested in developing and validating specific functional hypotheses.
Languageeng
Pub Type(s)Journal Article
Research Support, N.I.H., Extramural
PubMed ID19805138
  
Advertise on this site.