2Y9U
Structural basis of p63a SAM domain mutants involved in AEC syndrome
2Y9U の概要
| エントリーDOI | 10.2210/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: 21615690DOI: 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) |
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