4TX5
Crystal structure of Smac-DIABLO (in space group P65)
4TX5 の概要
| エントリーDOI | 10.2210/pdb4tx5/pdb |
| 分子名称 | Diablo homolog, mitochondrial, (4S)-2-METHYL-2,4-PENTANEDIOL, ACETATE ION, ... (4 entities in total) |
| 機能のキーワード | smac-diablo, apoptosis |
| 由来する生物種 | Homo sapiens (Human) |
| 細胞内の位置 | Mitochondrion : Q9NR28 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 44661.72 |
| 構造登録者 | |
| 主引用文献 | Mastrangelo, E.,Vachette, P.,Cossu, F.,Malvezzi, F.,Bolognesi, M.,Milani, M. The activator of apoptosis Smac-DIABLO acts as a tetramer in solution. Biophys.J., 108:714-723, 2015 Cited by PubMed Abstract: Smac-DIABLO in its mature form (20.8 kDa) binds to baculoviral IAP repeat (BIR) domains of inhibitor of apoptosis proteins (IAPs) releasing their inhibitory effects on caspases, thus promoting cell death. Despite its apparent molecular mass (∼100 kDa), Smac-DIABLO was held to be a dimer in solution, simultaneously targeting two distinct BIR domains. We report an extensive biophysical characterization of the protein alone and in complex with the X-linked IAP (XIAP)-BIR2-BIR3 domains. Our data show that Smac-DIABLO adopts a tetrameric assembly in solution and that the tetramer is able to bind two BIR2-BIR3 pairs of domains. Our small-angle x-ray scattering-based tetrameric model of Smac-DIABLO/BIR2-BIR3 highlights some conformational freedom of the complex that may be related to optimization of IAPs binding. PubMed: 25650938DOI: 10.1016/j.bpj.2014.11.3471 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.8 Å) |
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