5L3C
Human LSD1/CoREST: LSD1 E379K mutation
5L3C の概要
エントリーDOI | 10.2210/pdb5l3c/pdb |
分子名称 | Lysine-specific histone demethylase 1A, REST corepressor 1, FLAVIN-ADENINE DINUCLEOTIDE (3 entities in total) |
機能のキーワード | oxidoreductase-repressor complex, histone demethylase, chromatin, flavin, fad, oxidoreductase/repressor |
由来する生物種 | Homo sapiens (Human) 詳細 |
細胞内の位置 | Nucleus : O60341 Q9UKL0 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 146899.03 |
構造登録者 | Pilotto, S.,Speranzini, V.,Marabelli, C.,Mattevi, A. (登録日: 2016-04-06, 公開日: 2016-05-04, 最終更新日: 2024-01-10) |
主引用文献 | Pilotto, S.,Speranzini, V.,Marabelli, C.,Rusconi, F.,Toffolo, E.,Grillo, B.,Battaglioli, E.,Mattevi, A. LSD1/KDM1A mutations associated to a newly described form of intellectual disability impair demethylase activity and binding to transcription factors. Hum.Mol.Genet., 25:2578-2587, 2016 Cited by PubMed Abstract: Genetic diseases often lead to rare and severe syndromes and the identification of the genetic and protein alterations responsible for the pathogenesis is essential to understand both the physiological and pathological role of the gene product. Recently, de novo variants have been mapped on the gene encoding for the lysine-specific histone demethylase 1 (LSD1)/lysine(K)-specific histone demethylase 1A in three patients characterized by a new genetic disorder. We have analyzed the effects of these pathological mutations on the structure, stability and activity of LSD1 using both in vitro and cellular approaches. The three mutations (Glu403Lys, Asp580Gly and Tyr785His) affect active-site residues and lead to a partial impairment of catalytic activity. They also differentially perturb the ability of LSD1 to engage transcription factors that orchestrate key developmental programs. Moreover, cellular data indicate a decrease in the protein cellular half-life. Taken together, these results demonstrate the relevance of LSD1 in gene regulation and how even moderate alterations in its stability, catalytic activity and binding properties can strongly affect organism development. This depicts a perturbed interplay of catalytic and non-catalytic processes at the origin of the pathology. PubMed: 27094131DOI: 10.1093/hmg/ddw120 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (3.31 Å) |
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