Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Home
Search
Quick Search
Advanced
Fulltext
Browse
Collections
Persons
My eDoc
Session History
Login
Name:
Password:
Documentation
Help
Support Wiki
Direct access to
document ID:


          Institute: MPI für molekulare Genetik     Collection: Independent Junior Research Groups (Otto-Warburg-Laboratory)     Display Documents



  history
ID: 459936.0, MPI für molekulare Genetik / Independent Junior Research Groups (Otto-Warburg-Laboratory)
Detection of alpha-rod protein repeats using a neural network and application to Huntingtin
Authors:Palidwor, Gareth A.; Shcherbinin, Sergey; Huska, Matthew R.; Rasko, Tamas; Stelzl, Ulrich; Arumughan, Anup; Foulle, Raphaele; Porras, Pablo; Sanchez-Pulido, Luis; Wanker, Erich E.; Andrade-Navarro, Miguel A.
Language:English
Date of Publication (YYYY-MM-DD):2009-03-13
Title of Journal:PLoS Computational Biology
Volume:5
Issue / Number:3
Start Page:e1000304
End Page:e1000304
Copyright:© 2009 Palidwor et al
Review Status:not specified
Audience:Experts Only
Abstract / Description:A growing number of solved protein structures display an elongated structural domain, denoted here as alpha-rod, composed of stacked pairs of anti-parallel alpha-helices. Alpha-rods are flexible and expose a large surface, which makes them suitable for protein interaction. Although most likely originating by tandem duplication of a two-helix unit, their detection using sequence similarity between repeats is poor. Here, we show that alpha-rod repeats can be detected using a neural network. The network detects more repeats than are identified by domain databases using multiple profiles, with a low level of false positives (<10%). We identify alpha-rod repeats in approximately 0.4% of proteins in eukaryotic genomes. We then investigate the results for all human proteins, identifying alpha-rod repeats for the first time in six protein families, including proteins STAG1-3, SERAC1, and PSMD1-2 & 5. We also characterize a short version of these repeats in eight protein families of Archaeal, Bacterial, and Fungal species. Finally, we demonstrate the utility of these predictions in directing experimental work to demarcate three alpha-rods in huntingtin, a protein mutated in Huntington's disease. Using yeast two hybrid analysis and an immunoprecipitation technique, we show that the huntingtin fragments containing alpha-rods associate with each other. This is the first definition of domains in huntingtin and the first validation of predicted interactions between fragments of huntingtin, which sets up directions toward functional characterization of this protein. An implementation of the repeat detection algorithm is available as a Web server with a simple graphical output: http://www.ogic.ca/projects/ard. This can be further visualized using BiasViz, a graphic tool for representation of multiple sequence alignments.
Comment of the Author/Creator:email: Miguel.andrade@mdc-berlin.de
External Publication Status:published
Document Type:Article
Communicated by:OWL-Group
Affiliations:MPI für molekulare Genetik
External Affiliations:Ottawa Health Research Institute, Ottawa, Ontario, Canada
Medical Imaging Research Group, The University of British Columbia, Vancouver General Hospital, Vancouver, British Columbia, Canada
Max-Delbrück Center for Molecular Medicine, Berlin, Germany Functional Genetics Unit, Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom
Identifiers:DOI:10.1371/journal.pcbi.1000304
ISSN:1553-7358
URL:http://www.ploscompbiol.org/article/fetchObjectAtt...
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.