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Nucleic Acids Research, 2004, Vol. 32, Database issue D235-D239
© 2004 Oxford University Press

The SUPERFAMILY database in 2004: additions and improvements

Martin Madera*, Christine Vogel, Sarah K. Kummerfeld, Cyrus Chothia and Julian Gough1,2

MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK, 1 Department of Structural Biology, School of Medicine, Stanford University, Stanford, CA 94305-5125, USA and 2 RIKEN Genomic Sciences Centre, W121 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama 230-0045, Japan

*To whom correspondence should be addressed. Tel: +44 1223 402479; Fax: +44 1223 213556; Email: mm238{at}mrc-lmb.cam.ac.uk

The SUPERFAMILY database provides structural assignments to protein sequences and a framework for analysis of the results. At the core of the database is a library of profile Hidden Markov Models that represent all proteins of known structure. The library is based on the SCOP classification of proteins: each model corresponds to a SCOP domain and aims to represent an entire superfamily. We have applied the library to predicted proteins from all completely sequenced genomes (currently 154), the Swiss-Prot and TrEMBL databases and other sequence collections. Close to 60% of all proteins have at least one match, and one half of all residues are covered by assignments. All models and full results are available for download and online browsing at http://supfam.org. Users can study the distribution of their superfamily of interest across all completely sequenced genomes, investigate with which other superfamilies it combines and retrieve proteins in which it occurs. Alternatively, concentrating on a particular genome as a whole, it is possible first, to find out its superfamily composition, and secondly, to compare it with that of other genomes to detect superfamilies that are over- or under-represented. In addition, the webserver provides the following standard services: sequence search; keyword search for genomes, superfamilies and sequence identifiers; and multiple alignment of genomic, PDB and custom sequences.


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