Title :
Protein Subcomplexes—Molecular Machines With Highly Specialized Functions
Author :
Hollunder, Jens ; Beyer, Andreas ; Wilhelm, Thomas
Author_Institution :
Leibniz Inst. for Age Res., Fritz Lipmann Inst., Jena
fDate :
3/1/2007 12:00:00 AM
Abstract :
Complex cellular processes are accomplished by the concerted action of hierarchically organized functional modules. Protein complexes are major components which act as highly specialized molecular machines. Here we present a statistical procedure to find insightful substructures in protein complexes based on large-scale protein complex data: we identify statistically significant common protein subcomplexes (SCs) contained in different protein complexes. We analyze recently published data of the two model organisms Saccharomyces cerevisiae (four different data sets) and Escherichia coli, as well as human protein complex data. Our method identifies well-characterized protein assemblies with known functions which act as own functional entities in the cell. In addition, we also identified hitherto unknown functional entities that should be studied experimentally in future. We discuss two typical properties of protein subcomplexes: 1) subcomplexes are enriched with essential proteins (which implies that the whole SCs may be strongly conserved) and 2) SCs are functionally and spatially more homogeneous than the experimentally found protein assemblies. The latter property is exploited to propose functions for so far unknown proteins of S. cerevisiae
Keywords :
biology computing; cellular biophysics; microorganisms; molecular biophysics; proteins; statistical analysis; Escherichia coli; Saccharomyces cerevisiae; complex cellular processes; highly specialized functions; large-scale protein complex data; molecular machines; protein subcomplexes; statistical methods; Assembly; Biology computing; Biomedical engineering; Data analysis; Frequency; Humans; Large-scale systems; Organisms; Proteins; Systems biology; Gene annotation; molecular machines; protein complex; protein–protein interaction; Algorithms; Amino Acid Motifs; Computers, Molecular; Nanotechnology; Protein Interaction Mapping; Proteins; Sequence Alignment; Sequence Analysis, Protein; Structure-Activity Relationship;
Journal_Title :
NanoBioscience, IEEE Transactions on
DOI :
10.1109/TNB.2007.891884