1LG7
Crystal structure of Vesicular Stomatitis Virus Matrix Protein
1LG7 の概要
| エントリーDOI | 10.2210/pdb1lg7/pdb |
| 分子名称 | VSV matrix protein (2 entities in total) |
| 機能のキーワード | virus matrix, viral protein |
| 由来する生物種 | Vesicular stomatitis virus |
| 細胞内の位置 | Virion membrane; Peripheral membrane protein: Q8B0H2 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 21011.04 |
| 構造登録者 | |
| 主引用文献 | Gaudier, M.,Gaudin, Y.,Knossow, M. Crystal structure of vesicular stomatitis virus matrix protein. EMBO J., 21:2886-2892, 2002 Cited by PubMed Abstract: The vesicular stomatitis virus (VSV) matrix protein (M) interacts with cellular membranes, self-associates and plays a major role in virus assembly and budding. We present the crystallographic structure, determined at 1.96 A resolution, of a soluble thermolysin resistant core of VSV M. The fold is a new fold shared by the other vesiculovirus matrix proteins. The structure accounts for the loss of stability of M temperature-sensitive mutants deficient in budding, and reveals a flexible loop protruding from the globular core that is important for self-assembly. Membrane floatation shows that, together with the M lysine-rich N-terminal peptide, a second domain of the protein is involved in membrane binding. Indeed, the structure reveals a hydrophobic surface located close to the hydrophobic loop and surrounded by conserved basic residues that may constitute this domain. Lastly, comparison of the negative-stranded virus matrix proteins with retrovirus Gag proteins suggests that the flexible link between their major membrane binding domain and the rest of the structure is a common feature shared by these proteins involved in budding and virus assembly. PubMed: 12065402DOI: 10.1093/emboj/cdf284 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.96 Å) |
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