脱甲基酶
机制(生物学)
赖氨酸
酶
化学
生物化学
计算生物学
生物
氨基酸
哲学
认识论
DNA
组蛋白
作者
Ruchi Anand,Ronen Marmorstein
标识
DOI:10.1074/jbc.r700027200
摘要
The discovery of histone-demethylating enzymes has revealed yet another reversible histone modification mark. In this review, we describe the structural and chemical insights that we have now derived underlying the activity of these enzymes. The recent co-crystal structures of LSD1 bound to a proparylamine-derivatized histone H3 peptide and JHDM structures bound to two different methylated histone H3 peptides illustrate the steric requirements and structural basis for substrate specificity.
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