Function Diversity Within Folds and Superfamilies View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

2009

AUTHORS

Benoit H. Dessailly , Christine A. Orengo

ABSTRACT

With the advent of structural genomics initiatives, increasing numbers of three-dimensional structures are available for proteins of unknown function. However, the extent to which structural information helps understanding function is still a matter of debate. Here, the value of detecting structural relationships at differ ent levels (typically, fold and superfamily) for transferring functional annotations between proteins is reviewed. First, function diversity of proteins sharing the same fold is investigated, and it is shown that although the identification of a fold can in some cases provide clues on functional properties, the diversity of functions within a fold can be such that this information is very limited for some particularly diverse folds (e.g. super-folds). Next, since structural data can help detecting homology in the absence of sequence similarity, function diversity between proteins from the same superfamily (homologous proteins) is analysed. The evolutionary causes and the mechanisms that have generated the observed functional diversity between related proteins are discussed, and helpful tools for the correlated analysis of struc ture, function and evolution are reviewed. More... »

PAGES

143-166

Book

TITLE

From Protein Structure to Function with Bioinformatics

ISBN

978-1-4020-9057-8
978-1-4020-9058-5

Author Affiliations

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-1-4020-9058-5_6

DOI

http://dx.doi.org/10.1007/978-1-4020-9058-5_6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1040918706


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