Literature DB >> 11839303

Continuum secondary structure captures protein flexibility.

Claus A F Andersen1, Arthur G Palmer, Søren Brunak, Burkhard Rost.   

Abstract

The DSSP program assigns protein secondary structure to one of eight states. This discrete assignment cannot describe the continuum of thermal fluctuations. Hence, a continuous assignment is proposed. Technically, the continuum results from averaging over ten discrete DSSP assignments with different hydrogen bond thresholds. The final continuous assignment for a single NMR model successfully reflected the structural variations observed between all NMR models in the ensemble. The structural variations between NMR models were verified to correlate with thermal motion; these variations were captured by the continuous assignments. Because the continuous assignment reproduces the structural variation between many NMR models from one single model, functionally important variation can be extracted from a single X-ray structure. Thus, continuous assignments of secondary structure may affect future protein structure analysis, comparison, and prediction.

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Year:  2002        PMID: 11839303     DOI: 10.1016/s0969-2126(02)00700-1

Source DB:  PubMed          Journal:  Structure        ISSN: 0969-2126            Impact factor:   5.006


  51 in total

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7.  Protein conformational flexibility prediction using machine learning.

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8.  Alpha-Helix folding in the presence of structural constraints.

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9.  Computational modeling on the recognition of the HRE motif by HIF-1: molecular docking and molecular dynamics studies.

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