Literature DB >> 24002904

Geometry motivated alternative view on local protein backbone structures.

Jan Zacharias1, Ernst Walter Knapp.   

Abstract

We present an alternative to the classical Ramachandran plot (R-plot) to display local protein backbone structure. Instead of the (φ, ψ)-backbone angles relating to the chemical architecture of polypeptides generic helical parameters are used. These are the rotation or twist angle ϑ and the helical rise parameter d. Plots with these parameters provide a different view on the nature of local protein backbone structures. It allows to display the local structures in polar (d, ϑ)-coordinates, which is not possible for an R-plot, where structural regimes connected by periodicity appear disconnected. But there are other advantages, like a clear discrimination of the handedness of a local structure, a larger spread of the different local structure domains--the latter can yield a better separation of different local secondary structure motives--and many more. Compared to the R-plot we are not aware of any major disadvantage to classify local polypeptide structures with the (d, ϑ)-plot, except that it requires some elementary computations. To facilitate usage of the new (d, ϑ)-plot for protein structures we provide a web application (http://agknapp.chemie.fu-berlin.de/secsass), which shows the (d, ϑ)-plot side-by-side with the R-plot.
© 2013 The Protein Society.

Keywords:  (d, ϑ)-plot; alternative Ramachandran plot; backbone conformation plot; generic helix parameters; protein geometry; protein secondary structure

Mesh:

Substances:

Year:  2013        PMID: 24002904      PMCID: PMC3831682          DOI: 10.1002/pro.2364

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


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Review 7.  Conformation of polypeptides and proteins.

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