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      Secondary-structure matching (SSM), a new tool for fast protein structure alignment in three dimensions.

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          Abstract

          The present paper describes the SSM algorithm of protein structure comparison in three dimensions, which includes an original procedure of matching graphs built on the protein's secondary-structure elements, followed by an iterative three-dimensional alignment of protein backbone Calpha atoms. The SSM results are compared with those obtained from other protein comparison servers, and the advantages and disadvantages of different scores that are used for structure recognition are discussed. A new score, balancing the r.m.s.d. and alignment length Nalign, is proposed. It is found that different servers agree reasonably well on the new score, while showing considerable differences in r.m.s.d. and Nalign.

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          Author and article information

          Journal
          Acta Crystallogr D Biol Crystallogr
          Acta crystallographica. Section D, Biological crystallography
          International Union of Crystallography (IUCr)
          0907-4449
          0907-4449
          Dec 2004
          : 60
          : Pt 12 Pt 1
          Affiliations
          [1 ] European Bioinformatics Institute, Genome Campus, Hinxton, Cambridge CB10 1SD, England. keb@ebi.ac.uk
          Article
          S0907444904026460
          10.1107/S0907444904026460
          15572779
          217125bd-1c4b-4f41-8e74-df9318394fb6
          History

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