Research Article
Quaternion-based definition of protein secondary structure straightness and its relationship to Ramachandran angles
Article first published online: 9 MAY 2011
DOI: 10.1002/prot.23037
Copyright © 2011 Wiley-Liss, Inc.
Issue

Proteins: Structure, Function, and Bioinformatics
Volume 79, Issue 7, pages 2172–2180, July 2011
Additional Information
How to Cite
Hanson, R. M., Kohler, D. and Braun, S. G. (2011), Quaternion-based definition of protein secondary structure straightness and its relationship to Ramachandran angles. Proteins, 79: 2172–2180. doi: 10.1002/prot.23037
Publication History
- Issue published online: 10 JUN 2011
- Article first published online: 9 MAY 2011
- Accepted manuscript online: 22 MAR 2011 10:39AM EST
- Manuscript Accepted: 13 MAR 2011
- Manuscript Revised: 18 FEB 2011
- Manuscript Received: 26 JUL 2010
Funded by
- Howard Hughes Medical Institute
- St. Olaf College Lowell and Doris Kispert fund
- Abstract
- Article
- References
- Cited By
Keywords:
- DSSP;
- quantifying structural regularity;
- quaternion frames;
- identification of PDB anomalies
Abstract
We describe here definitions of “local helical axis” and “straightness” that are developed using a simple quaternion-based analysis of protein structure without resort to least-squares fitting. As part of this analysis, it is shown how quaternion differences can be visualized to depict accurately the local helical axis relating any two adjacent amino acid residues in standard, nonidealized proteins. Three different options for the definition of amino acid residue orientation in terms of quaternion frames are described. Two of these, the “Cα frame” and the “P frame,” are shown to be correlated strongly with a simple approximate measure derived solely from Ramachandran angles. The relationship between quaternion-based straightness and recognized DSSP-derived secondary structure motifs is discussed. Proteins 2011; © 2011 Wiley-Liss, Inc.

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