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2QND

Crystal Structure of the KH1-KH2 domains from human Fragile X Mental Retardation Protein

2QND の概要
エントリーDOI10.2210/pdb2qnd/pdb
分子名称FMR1 protein, MAGNESIUM ION (3 entities in total)
機能のキーワードkh domain, eukaryotic kh domains, tandem kh domains, type i kh domains, fragile x mental retardation protein, fmrp, rna binding protein
由来する生物種Homo sapiens (human)
詳細
タンパク質・核酸の鎖数2
化学式量合計32328.42
構造登録者
Valverde, R.,Regan, L. (登録日: 2007-07-18, 公開日: 2007-11-06, 最終更新日: 2024-10-30)
主引用文献Valverde, R.,Pozdnyakova, I.,Kajander, T.,Venkatraman, J.,Regan, L.
Fragile X mental retardation syndrome: structure of the KH1-KH2 domains of fragile X mental retardation protein.
Structure, 15:1090-1098, 2007
Cited by
PubMed Abstract: Fragile X syndrome is the most common form of inherited mental retardation in humans, with an estimated prevalence of about 1 in 4000 males. Although several observations indicate that the absence of functional Fragile X Mental Retardation Protein (FMRP) is the underlying basis of Fragile X syndrome, the structure and function of FMRP are currently unknown. Here, we present an X-ray crystal structure of the tandem KH domains of human FMRP, which reveals the relative orientation of the KH1 and KH2 domains and the location of residue Ile304, whose mutation to Asn is associated with a particularly severe incidence of Fragile X syndrome. We show that the Ile304Asn mutation both perturbs the structure and destabilizes the protein.
PubMed: 17850748
DOI: 10.1016/j.str.2007.06.022
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.9 Å)
構造検証レポート
Validation report summary of 2qnd
検証レポート(詳細版)ダウンロードをダウンロード

248942

件を2026-02-11に公開中

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