1SX2
Use of a Halide Binding Site to Bypass the 1000-atom Limit to Structure Determination by Direct Methods
1SX2 の概要
| エントリーDOI | 10.2210/pdb1sx2/pdb |
| 関連するPDBエントリー | 1SWY 1SWZ 1SX7 |
| 分子名称 | Lysozyme, RUBIDIUM ION, CHLORIDE ION, ... (5 entities in total) |
| 機能のキーワード | rb+ binding sites; ab initio direct methods, hydrolase |
| 由来する生物種 | Enterobacteria phage T4 |
| 細胞内の位置 | Host cytoplasm : P00720 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 19351.25 |
| 構造登録者 | |
| 主引用文献 | Mooers, B.H.,Matthews, B.W. Use of an ion-binding site to bypass the 1000-atom limit to structure determination by direct methods. Acta Crystallogr.,Sect.D, 60:1726-1737, 2004 Cited by PubMed Abstract: Proteins with more than 1000 non-H atoms and without heavy-atom prosthetic groups are very difficult to solve by ab initio direct methods. T4 lysozyme is being used to explore these limits. The protein has 1309 non-H atoms, seven S atoms, no disulfide bonds and no heavy-atom prosthetic group. It is recalcitrant to structure determination by direct methods using X-ray diffraction data to 0.97 A. It is shown here that it is possible to obtain a truly ab initio structure determination of a variant of the protein that has an Rb+ (Z = 37) binding site. Using diffraction data to 1.06 A resolution, the direct-methods programs SIR2002 and ACORN independently solved the structure in about 20 h. The bound Rb+, which contributes about 1.7% of the total scattering, does not appear to distort the structure or to inhibit refinement (R factor 12.1%). The phases obtained via SIR2002 or ACORN are in good agreement with those from a reference structure obtained from conventional molecular-substitution and refinement procedures (average error in the figure-of-merit-weighted phases of less than 25 degrees). Thus, proteins with more than 1000 atoms that include halide-binding or other such sites may be amenable to structure determination by ab initio direct methods. The direct-methods approaches are also compared with structure determination via use of the anomalous scattering of the Rb+ ion. As shown by examples, high-resolution structures determined by direct methods can be useful in highlighting regions of strain in the protein, including short hydrogen bonds and non-planar peptide groups. PubMed: 15388918DOI: 10.1107/S0907444904017020 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.06 Å) |
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