Skip Navigation


Bioinformatics Advance Access originally published online on February 2, 2005
Bioinformatics 2005 21(9):1853-1858; doi:10.1093/bioinformatics/bti303
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (Print PDF) Freely available
Right arrow All Versions of this Article:
21/9/1853    most recent
bti303v1
Right arrow Comments: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Comments are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (10)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Kahsay, R. Y.
Right arrow Articles by Liao, L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kahsay, R. Y.
Right arrow Articles by Liao, L.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2005. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions{at}oupjournals.org

An improved hidden Markov model for transmembrane protein detection and topology prediction and its applications to complete genomes

Robel Y. Kahsay 1, Guang Gao 1 and Li Liao 1,2,*

1Delaware Biotechnology Institute Newark, DE 19715, USA
2Department of Computer and Information Sciences, University of Delaware 103 Smith Hall, Newark, DE 19716, USA

*To whom correspondence should be addressed.

Motivation: Knowledge of the transmembrane helical topology can help identify binding sites and infer functions for membrane proteins. However, because membrane proteins are hard to solubilize and purify, only a very small amount of membrane proteins have structure and topology experimentally determined. This has motivated various computational methods for predicting the topology of membrane proteins.

Results: We present an improved hidden Markov model, TMMOD, for the identification and topology prediction of transmembrane proteins. Our model uses TMHMM as a prototype, but differs from TMHMM by the architecture of the submodels for loops on both sides of the membrane and also by the model training procedure. In cross-validation experiments using a set of 83 transmembrane proteins with known topology, TMMOD outperformed TMHMM and other existing methods, with an accuracy of 89% for both topology and locations. In another experiment using a separate set of 160 transmembrane proteins, TMMOD had 84% for topology and 89% for locations. When utilized for identifying transmembrane proteins from non-transmembrane proteins, particularly signal peptides, TMMOD has consistently fewer false positives than TMHMM does. Application of TMMOD to a collection of complete genomes shows that the number of predicted membrane proteins accounts for ~20–30% of all genes in those genomes, and that the topology where both the N- and C-termini are in the cytoplasm is dominant in these organisms except for Caenorhabditis elegans.

Availability: http://liao.cis.udel.edu/website/servers/TMMOD/

Contact: lliao{at}cis.udel.edu


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Bacteriol.Home page
P. Veiga, M. Erkelenz, E. Bernard, P. Courtin, S. Kulakauskas, and M.-P. Chapot-Chartier
Identification of the Asparagine Synthase Responsible for D-Asp Amidation in the Lactococcus lactis Peptidoglycan Interpeptide Crossbridge
J. Bacteriol., June 1, 2009; 191(11): 3752 - 3757.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
M. C. Walter, T. Rattei, R. Arnold, U. Guldener, M. Munsterkotter, K. Nenova, G. Kastenmuller, P. Tischler, A. Wolling, A. Volz, et al.
PEDANT covers all complete RefSeq genomes
Nucleic Acids Res., January 1, 2009; 37(suppl_1): D408 - D411.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
P. A. Belenky, T. G. Moga, and C. Brenner
Saccharomyces cerevisiae YOR071C Encodes the High Affinity Nicotinamide Riboside Transporter Nrt1
J. Biol. Chem., March 28, 2008; 283(13): 8075 - 8079.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. G. Kreft, L. Wang, and M. Hochstrasser
Membrane Topology of the Yeast Endoplasmic Reticulum-localized Ubiquitin Ligase Doa10 and Comparison with Its Human Ortholog TEB4 (MARCH-VI)
J. Biol. Chem., February 24, 2006; 281(8): 4646 - 4653.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.