Bioinformatics Advance Access published online on March 31, 2005
Bioinformatics, doi:10.1093/bioinformatics/bti420
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 School of Computing Sciences, University of East Anglia, Norwich, NR4 7TJ, UK
* To whom correspondence should be addressed.
Motivation: The current DynDom database of protein domain motions is a user-created database that suffers from selectivity and redundancy. The aim of the analysis presented here was to overcome both these limitations and to produce both a comprehensive and non-redundant description of domain movements from structures stored in the current protein data bank. Results: A multi-step procedure is applied that starts with grouping proteins in the structural databank into families based on sequence similarity. Multiple sequence alignment, conformational clustering, and a dimensional clustering method based on the Gram-Schmidt algorithm, are applied to members of each family to remove dynamic redundancy in their domain movements. Representative domain movements are described in terms of domains, hinge axes, and hinge-bending residues using the DynDom program. The results show that within an average family of 11.5 members there are on average only 1.31 different domain movements indicating a high redundancy in the movements these structures represent. This verifies earlier findings that domain movements are usually highly controlled. Despite the removal of this considerable redundancy the process has resulted in double the number of domain movements stored in the user-created database. The data is organised in a relational database with a web-interface. Availability: The database can be browsed and searched at: http://www.cmp.uea.ac.uk/dyndom.
Received February 4, 2005
Revised March 18, 2005
Accepted March 30, 2005
Article
A comprehensive and non-redundant database of protein domain movements
2 School of Computing Sciences, University of East Anglia, Norwich, NR4 7TJ, UK; School of Biological Sciences, University of East Anglia, Norwich, NR4 7TJ, UK
Steven Hayward, E-mail: sjh{at}cmp.uea.ac.uk
![]()
Abstract ![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
K.-i. Okazaki and S. Takada Dynamic energy landscape view of coupled binding and protein conformational change: Induced-fit versus population-shift mechanisms PNAS, August 12, 2008; 105(32): 11182 - 11187. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Nigham, L. Tucker-Kellogg, I. Mihalek, C. Verma, and D. Hsu pFlexAna: detecting conformational changes in remotely related proteins Nucleic Acids Res., July 1, 2008; 36(suppl_2): W246 - W251. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. K. Fyfe, S. L. Oza, A. H. Fairlamb, and W. N. Hunter Leishmania Trypanothione Synthetase-Amidase Structure Reveals a Basis for Regulation of Conflicting Synthetic and Hydrolytic Activities J. Biol. Chem., June 20, 2008; 283(25): 17672 - 17680. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Oria-Hernandez, H. Riveros-Rosas, and L. Ramirez-Silva Dichotomic Phylogenetic Tree of the Pyruvate Kinase Family: K+-DEPENDENT AND -INDEPENDENT ENZYMES J. Biol. Chem., October 13, 2006; 281(41): 30717 - 30724. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Hayward and A. Kitao Molecular Dynamics Simulations of NAD+-Induced Domain Closure in Horse Liver Alcohol Dehydrogenase Biophys. J., September 1, 2006; 91(5): 1823 - 1831. [Abstract] [Full Text] [PDF] |
||||



