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2Y9U

Structural basis of p63a SAM domain mutants involved in AEC syndrome

2Y9U の概要
エントリーDOI10.2210/pdb2y9u/pdb
関連するPDBエントリー1RG6 2Y9T
分子名称TUMOR PROTEIN 63, SULFATE ION (3 entities in total)
機能のキーワードapoptosis, sterile alpha motif, 5-helix bundle, mutations, aec syndrome
由来する生物種HOMO SAPIENS (HUMAN)
細胞内の位置Nucleus : Q9H3D4
タンパク質・核酸の鎖数1
化学式量合計8000.99
構造登録者
Sathyamurthy, A.,Freund, S.M.V.,Johnson, C.M.,Allen, M.D. (登録日: 2011-02-16, 公開日: 2011-08-03, 最終更新日: 2024-05-08)
主引用文献Sathyamurthy, A.,Freund, S.M.V.,Johnson, C.M.,Allen, M.D.,Bycroft, M.
Structural Basis of P63Alpha Sam Domain Mutants Involved in Aec Syndrome.
FEBS J., 278:2680-, 2011
Cited by
PubMed Abstract: p63 is a member of the p53 tumour suppressor family that includes p73. The p63 gene encodes a protein comprising an N-terminal transactivation domain, a DNA binding domain and an oligomerization domain, but varies in the organization of the C-terminus as a result of complex alternative splicing. p63α contains a C-terminal sterile α motif (SAM) domain that is thought to function as a protein-protein interaction domain. Several missense and heterozygous frame shift mutations, encoded within exon 13 and 14 of the p63 gene, have been identified in the p63α SAM domain in patients suffering from ankyloblepharon-ectodermal dysplasia-clefting syndrome. Here we report the solution and high resolution crystal structures of the p63α SAM domain and investigate the effect of several mutations (L553F/V, C562G/W, G569V, Q575L and I576T) on the stability of the domain. The possible effects of other mutations are also discussed.
PubMed: 21615690
DOI: 10.1111/J.1742-4658.2011.08194.X
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.6 Å)
構造検証レポート
Validation report summary of 2y9u
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-22に公開中

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