The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
NLStradamus: a simple Hidden Markov Model for nuclear localization signal prediction
Open accessAbstract
Background: Nuclear localization signals (NLSs) are stretches of residues within a protein that are important for the regulated nuclear import of the protein. Of the many import pathways that exist in yeast, the best characterized is termed the 'classical' NLS pathway. The classical NLS contains specific patterns of basic residues and computational methods have been designed to predict the location of these motifs on proteins. The consensus sequences, or patterns, for the other import pathways are less well-understood. Results: In this paper, we present an analysis of characterized NLSs in yeast, and find, despite the large number of nuclear import pathways, that NLSs seem to show similar patterns of amino acid residues. We test current prediction methods and observe a low true positive rate. We therefore suggest an approach using hidden Markov models (HMMs) to predict novel NLSs in proteins. We show that our method is able to consistently find 37% of the NLSs with a low false positive rate and that our method retains its true positive rate outside of the yeast data set used for the training parameters. Conclusion: Our implementation of this model, NLStradamus, is made available at: http://www.moseslab.csb.utoronto.ca/NLStradamus/
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Cites
Comparison of the predicted and observed secondary structure of T4 phage lysozyme
Matthews, B. W. (1975) · Biochimica et Biophysica Acta (BBA) - Protein Structure · doi:10.1016/0005-2795(75)90109-9 · Cited by 5,399 · cited 2×
“We also computed the Matthews Correlation Coefficient [14] and found that it was 0.55, similar to recent results for a predictor of nuclear export signals [15].”
MethodResultInfluentialNakai, K., & Horton, P. (1999) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(98)01336-x · Cited by 2,181 · cited 1×
“PSORT [7] accurately predicts protein localization by including heuristic scores based on residues frequencies, protein domains as well as motifs.”
MethodAssessing computational tools for the discovery of transcription factor binding sites
Tompa, M., Li, N., Bailey, T. L., Church, G. M., De Moor, B., Eskin, E., Favorov, A. V., Frith, M. C., Fu, Y., Kent, W. J., et al. (2005) · Nature Biotechnology · doi:10.1038/nbt1053 · Cited by 1,268
Dyskeratosis congenita in all its forms
Dokal, I. (2000) · British Journal of Haematology · doi:10.1046/j.1365-2141.2000.02109.x · Cited by 575
Fontes, M. R. M., Teh, T., & Kobe, B. (2000) · Journal of Molecular Biology · doi:10.1006/jmbi.2000.3642 · Cited by 398
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Wang, Y., Guo, Y. R., Liu, K., Yin, Z., Liu, R., Xia, Y., Tan, L., Yang, P., Lee, J.-H., Li, X.-J., et al. (2017) · Nature · doi:10.1038/nature25003 · Cited by 567
Types of nuclear localization signals and mechanisms of protein import into the nucleus
Lu, J., Wu, T., Zhang, B., Liu, S., Song, W., Qiao, J., & Ruan, H. (2021) · Cell Communication and Signaling · doi:10.1186/s12964-021-00741-y · Cited by 459
Liu, Z., Liu, G., Ha, D. P., Wang, J., Xiong, M., & Lee, A. S. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2303448120 · Cited by 137
Heat Shock Protein 90 Is Required for Conidiation and Cell Wall Integrity in Aspergillus fumigatus
Lamoth, F., Juvvadi, P. R., Fortwendel, J. R., & Steinbach, W. J. (2012) · Eukaryotic Cell · doi:10.1128/ec.00032-12 · Cited by 136
Gan, P., Narusaka, M., Kumakura, N., Tsushima, A., Takano, Y., Narusaka, Y., & Shirasu, K. (2016) · Genome Biology and Evolution · doi:10.1093/gbe/evw089 · Cited by 98
Metadata
- Authors
- Nguyen Ba, A. N., Pogoutse, A., Provart, N., & Moses, A. M.
- Venue
- BMC Bioinformatics
- Published
- 2009-06-29
- Volume
- 10
- Issue
- 1
- Pages
- 202-202
- ISSN
- 1471-2105 (ISSN-L)
- OpenAlex
- W2111607030
- Cited by
- 703
- References
- 5
- FWCI
- 4.56
- Type
- journal article
- Language
- en
- Open access
- gold
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