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• W4387203411 endingPage "215" @default.
• W4387203411 startingPage "195" @default.
• W4387203411 abstract "The malignant brain tumor (MBT) domain is a conserved protein domain that recognizes the mono- and di-methylated, but not tri-methylated, lysine residues in proteins. Nine members of mammalian MBT proteins, originating from three conserved Drosophila proteins, L(3)MBT, SCM, and SFMBT, were identified that contain multiple tandem MBT repeats to play critical roles in multiple biological processes, including tumor suppression, development, transcriptional control, and cell fate determination. Although these MBT proteins are considered as putative methyl-lysine readers for histones, emerging evidence indicates that one function of these proteins is to read the methylated lysine residues in nonhistone proteins to regulate a wide variety of biological processes, including regulation of epigenetic DNA methylation, transcriptional control of cell cycle progression, and maintenance of pluripotency and self-renewal of embryonic stem cells." @default.
• W4387203411 created "2023-09-30" @default.
• W4387203411 creator A5003759585 @default.
• W4387203411 creator A5083369904 @default.
• W4387203411 date "2024-01-01" @default.
• W4387203411 modified "2023-10-14" @default.
• W4387203411 title "The MBT proteins: Methyl-lysine readers for stem cells, development, and tumors" @default.
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• W4387203411 doi "https://doi.org/10.1016/b978-0-12-823376-4.00005-7" @default.

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