Structural Characterization of the Human Proteome

• DOI: 10.1101/gr.221202
• Publication Date: 2002-11-04T23:41:24Z
• Authors: Arne Müller; Robert M. MacCallum; Michael J.E. Ster...
• Keywords: 0303 health sciences; Saccharomyces cerevisiae Proteins; Proteome; Archaeal Proteins; Escherichia coli Proteins; Genetic Diseases, Inborn; Membrane Proteins; Online Systems; Markov Chains; 03 medical and health sciences; Bacterial Proteins; Gene Duplication; Databases, Genetic; Animals; Drosophila Proteins; Humans; Caenorhabditis elegans Proteins; Protein Structure, Quaternary; Algorithms; Phylogeny

This paper reports an analysis of the encoded proteins (the proteome) of the genomes of human, fly, worm, yeast, and representatives of bacteria and archaea in terms of the three-dimensional structures of their globular domains together with a general sequence-based study. We show that 39% of the human proteome can be assigned to known structures. We estimate that for 77% of the proteome, there is some functional annotation, but only 26% of the proteome can be assigned to standard sequence motifs that characterize function. Of the human protein sequences, 13% are transmembrane proteins, but only 3% of the residues in the proteome form membrane-spanning regions. There are substantial differences in the composition of globular domains of transmembrane proteins between the proteomes we have analyzed. Commonly occurring structural superfamilies are identified within the proteome. The frequencies of these superfamilies enable us to estimate that 98% of the human proteome evolved by domain duplication, with four of the 10 most duplicated superfamilies specific for multicellular organisms. The zinc-finger superfamily is massively duplicated in human compared to fly and worm, and occurrence of domains in repeats is more common in metazoa than in single cellular organisms. Structural superfamilies over- and underrepresented in human disease genes have been identified. Data and results can be downloaded and analyzed via web-based applications athttp://www.sbg.bio.ic.ac.uk.[Supplemental material is available online at http://www.genome.org.]