Literature DB >> 23108912

When a domain is not a domain, and why it is important to properly filter proteins in databases: conflicting definitions and fold classification systems for structural domains make filtering of such databases imperative.

Clare-Louise Towse1, Valerie Daggett.   

Abstract

Membership in a protein domain database does not a domain make; a feature we realized when generating a consensus view of protein fold space with our consensus domain dictionary (CDD). This dictionary was used to select representative structures for characterization of the protein dynameome: the Dynameomics initiative. Through this endeavor we rejected a surprising 40% of the 1,695 folds in the CDD as being non-autonomous folding units. Although some of this was due to the challenges of grouping similar fold topologies, the dissonance between the cataloguing and structural qualification of protein domains remains surprising. Another potential factor is previously overlooked intrinsic disorder; predictions suggest that 40% of proteins have either local or global disorder. One thing is clear, filtering a structural database and ensuring a consistent definition for protein domains is crucial, and caution is prescribed when generalizations of globular domains are drawn from unfiltered protein domain datasets.
Copyright © 2012 WILEY Periodicals, Inc.

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Year:  2012        PMID: 23108912      PMCID: PMC3576730          DOI: 10.1002/bies.201200116

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  55 in total

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Authors:  Anthony L Fink
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Authors:  C A Orengo; F M Pearl; J E Bray; A E Todd; A C Martin; L Lo Conte; J M Thornton
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7.  The pairwise energy content estimated from amino acid composition discriminates between folded and intrinsically unstructured proteins.

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Authors:  H Jane Dyson; Peter E Wright
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Journal:  Nucleic Acids Res       Date:  2011-11-16       Impact factor: 16.971

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  4 in total

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2.  Shared unfolding pathways of unrelated immunoglobulin-like β-sandwich proteins.

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Journal:  Protein Eng Des Sel       Date:  2019-12-31       Impact factor: 1.650

3.  New Dynamic Rotamer Libraries: Data-Driven Analysis of Side-Chain Conformational Propensities.

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4.  Conserved patterns and interactions in the unfolding transition state across SH3 domain structural homologues.

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Journal:  Protein Sci       Date:  2020-11-26       Impact factor: 6.993

  4 in total

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