期刊
EPIGENOMICS
卷 1, 期 1, 页码 163-175出版社
FUTURE MEDICINE LTD
DOI: 10.2217/EPI.09.3
关键词
hidden Markov model profiling; methyltransferases; protein methylation; RNA methylation; S-adenosylmethionine; SET domain; SPOUT domain
资金
- National Institutes of Health [GM026020]
- UCLA [GM008496]
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R37GM026020, R01GM026020, T32GM008496] Funding Source: NIH RePORTER
Methylation of DNA, protein and even RNA species are integral processes in epigenesis. Enzymes that catalyze these reactions using the donor S-adenosylmethionine fall into several structurally distinct classes. The members in each class share sequence similarity that can be used to identify additional methyltransferases. Here, we characterize these classes and in silico approaches to infer protein function. Computational methods, such as hidden Markov model profiling and the Multiple Motif Scanning program, can be used to analyze known methyltransferases and relay information into the prediction of new ones. In some cases, the substrate of methylation can be inferred from hidden Markov model sequence similarity networks. Functional identification of these candidate species is much more difficult; we discuss one biochemical approach.
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