Prediction of the human membrane proteome
- PMID: 20175080
- DOI: 10.1002/pmic.200900258
Prediction of the human membrane proteome
Abstract
Membrane proteins are key molecules in the cell, and are important targets for pharmaceutical drugs. Few three-dimensional structures of membrane proteins have been obtained, which makes computational prediction of membrane proteins crucial for studies of these key molecules. Here, seven membrane protein topology prediction methods based on different underlying algorithms, such as hidden Markov models, neural networks and support vector machines, have been used for analysis of the protein sequences from the 21,416 annotated genes in the human genome. The number of genes coding for a protein with predicted alpha-helical transmembrane region(s) ranged from 5508 to 7651, depending on the method used. Based on a majority decision method, we estimate 5539 human genes to code for membrane proteins, corresponding to approximately 26% of the human protein-coding genes. The largest fraction of these proteins has only one predicted transmembrane region, but there are also many proteins with seven predicted transmembrane regions, including the G-protein coupled receptors. A visualization tool displaying the topologies suggested by the eight prediction methods, for all predicted membrane proteins, is available on the public Human Protein Atlas portal (www.proteinatlas.org).
Similar articles
-
Evaluation of methods for predicting the topology of beta-barrel outer membrane proteins and a consensus prediction method.BMC Bioinformatics. 2005 Jan 12;6:7. doi: 10.1186/1471-2105-6-7. BMC Bioinformatics. 2005. PMID: 15647112 Free PMC article.
-
Discrimination of outer membrane proteins using support vector machines.Bioinformatics. 2005 Dec 1;21(23):4223-9. doi: 10.1093/bioinformatics/bti697. Epub 2005 Oct 4. Bioinformatics. 2005. PMID: 16204348
-
[Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].Yi Chuan Xue Bao. 2004 May;31(5):431-43. Yi Chuan Xue Bao. 2004. PMID: 15478601 Chinese.
-
Topology prediction of helical transmembrane proteins: how far have we reached?Curr Protein Pept Sci. 2010 Nov;11(7):550-61. doi: 10.2174/138920310794109184. Curr Protein Pept Sci. 2010. PMID: 20887261 Review.
-
Protein engineering methods applied to membrane protein targets.Protein Eng Des Sel. 2013 Feb;26(2):91-100. doi: 10.1093/protein/gzs079. Epub 2012 Oct 31. Protein Eng Des Sel. 2013. PMID: 23118339 Review.
Cited by
-
Therapeutic Monoclonal Antibodies against Cancer: Present and Future.Cells. 2023 Dec 14;12(24):2837. doi: 10.3390/cells12242837. Cells. 2023. PMID: 38132155 Free PMC article. Review.
-
Structural genomics plucks high-hanging membrane proteins.Curr Opin Struct Biol. 2012 Jun;22(3):326-32. doi: 10.1016/j.sbi.2012.05.002. Epub 2012 May 21. Curr Opin Struct Biol. 2012. PMID: 22622032 Free PMC article. Review.
-
Polar residues and their positional context dictate the transmembrane domain interactions of influenza A neuraminidases.J Biol Chem. 2013 Apr 12;288(15):10652-60. doi: 10.1074/jbc.M112.440230. Epub 2013 Feb 27. J Biol Chem. 2013. PMID: 23447533 Free PMC article.
-
A Combined Omics Approach to Generate the Surface Atlas of Human Naive CD4+ T Cells during Early T-Cell Receptor Activation.Mol Cell Proteomics. 2015 Aug;14(8):2085-102. doi: 10.1074/mcp.M114.045690. Epub 2015 May 19. Mol Cell Proteomics. 2015. PMID: 25991687 Free PMC article.
-
Paracellular epithelial sodium transport maximizes energy efficiency in the kidney.J Clin Invest. 2016 Jul 1;126(7):2509-18. doi: 10.1172/JCI83942. Epub 2016 May 23. J Clin Invest. 2016. PMID: 27214555 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources