Literature DB >> 12880206

Target selection and determination of function in structural genomics.

James D Watson1, Annabel E Todd, James Bray, Roman A Laskowski, Aled Edwards, Andrzej Joachimiak, Christine A Orengo, Janet M Thornton.   

Abstract

The first crucial step in any structural genomics project is the selection and prioritization of target proteins for structure determination. There may be a number of selection criteria to be satisfied, including that the proteins have novel folds, that they be representatives of large families for which no structure is known, and so on. The better the selection at this stage, the greater is the value of the structures obtained at the end of the experimental process. This value can be further enhanced once the protein structures have been solved if the functions of the given proteins can also be determined. Here we describe the methods used at either end of the experimental process: firstly, sensitive sequence comparison techniques for selecting a high-quality list of target proteins, and secondly the various computational methods that can be applied to the eventual 3D structures to determine the most likely biochemical function of the proteins in question.

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Year:  2003        PMID: 12880206      PMCID: PMC3366504          DOI: 10.1080/1521654031000123385

Source DB:  PubMed          Journal:  IUBMB Life        ISSN: 1521-6543            Impact factor:   3.885


  63 in total

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3.  trEST, trGEN and Hits: access to databases of predicted protein sequences.

Authors:  M Pagni; C Iseli; T Junier; L Falquet; V Jongeneel; P Bucher
Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

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Authors:  R L Tatusov; D A Natale; I V Garkavtsev; T A Tatusova; U T Shankavaram; B S Rao; B Kiryutin; M Y Galperin; N D Fedorova; E V Koonin
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6.  ProTarget: automatic prediction of protein structure novelty.

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7.  Structural and functional studies of S-adenosyl-L-methionine binding proteins: a ligand-centric approach.

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10.  Towards a comprehensive structural coverage of completed genomes: a structural genomics viewpoint.

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