Uncovering the Human Methyltransferasome

被引:225
作者
Petrossian, Tanya C.
Clarke, Steven G. [1 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
SET-DOMAIN PROTEIN; ISOPRENYLCYSTEINE CARBOXYL METHYLTRANSFERASE; SACCHAROMYCES-CEREVISIAE; S-ADENOSYLMETHIONINE; HISTONE METHYLTRANSFERASE; LYSINE METHYLTRANSFERASES; STRUCTURE PREDICTION; CRYSTAL-STRUCTURE; METHYLATION; IDENTIFICATION;
D O I
10.1074/mcp.M110.000976
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
We present a comprehensive analysis of the human methyltransferasome. Primary sequences, predicted secondary structures, and solved crystal structures of known methyltransferases were analyzed by hidden Markov models, Fisher-based statistical matrices, and fold recognition prediction-based threading algorithms to create a model, or profile, of each methyltransferase superfamily. These profiles were used to scan the human proteome database and detect novel methyltransferases. 208 proteins in the human genome are now identified as known or putative methyltransferases, including 38 proteins that were not annotated previously. To date, 30% of these proteins have been linked to disease states. Possible substrates of methylation for all of the SET domain and SPOUT methyltransferases as well as 100 of the 131 seven-beta-strand methyltransferases were surmised from sequence similarity clusters based on alignments of the substrate-specific domains. Molecular & Cellular Proteomics 10: 10.1074/mcp.M110.000976, 1-12, 2011.
引用
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页数:12
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