4UM4
STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM ESCHERICHIA COLI IN COMPLEX WITH SULFATE
4UM4 の概要
| エントリーDOI | 10.2210/pdb4um4/pdb |
| 分子名称 | INORGANIC PYROPHOSPHATASE, SULFATE ION (3 entities in total) |
| 機能のキーワード | hydrolase |
| 由来する生物種 | ESCHERICHIA COLI |
| 細胞内の位置 | Cytoplasm : P0A7A9 |
| タンパク質・核酸の鎖数 | 3 |
| 化学式量合計 | 59473.78 |
| 構造登録者 | |
| 主引用文献 | Campos-Acevedo, A.A.,Diaz-Vilchis, A.,Sotelo-Mundo, R.R.,Rudino-Pinera, E. First attempts to crystallize a non-homogeneous sample of thioredoxin from Litopenaeus vannamei: What to do when you have diffraction data of a protein that is not the target? Biochem Biophys Rep, 8:284-289, 2016 Cited by PubMed Abstract: The importance of sample homogeneity and purity in protein crystallization is essential to obtain high-quality diffracting crystals. Here, in an attempt to determine the crystal structure of thioredoxin 1 from whiteleg shrimp (Trx), we inadvertently crystallized the hexameric inorganic pyrophosphatase of (E-PPase) from a non-homogeneous sample product during the initial over-expression steps and partial purification of Trx. The structure determination and identification of the crystallized protein were derived from several clues: the failures in the Molecular Replacement (MR) trials using Trx coordinates as a search model, the unit cell parameters and space group determination, and essentially by the use of the program . After using the previously deposited E-PPase structure (PDB entry 1mjw) as a search model and the correct space group assignation, the MR showed an E-PPase complexed with SO with small changes in the sulfate ion binding region when it compares to previously deposited E-PPases in the PDB. This work stresses the importance of protein purity to avoid the risk of crystallizing a contaminant protein or how pure need to be a protein sample in order to increase the possibility to obtain crystals, but also serves as a reminder that crystallization is by itself a purification process and how the program can be useful in the crystal structure determination of previously deposited structures in the PDB. PubMed: 28955968DOI: 10.1016/j.bbrep.2016.09.011 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.65 Å) |
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