1AYP
A PROBE MOLECULE COMPOSED OF SEVENTEEN PERCENT OF TOTAL DIFFRACTING MATTER GIVES CORRECT SOLUTIONS IN MOLECULAR REPLACEMENT
1AYP の概要
エントリーDOI | 10.2210/pdb1ayp/pdb |
分子名称 | PHOSPHOLIPASE A2, CALCIUM ION, 1-OCTADECYL-2-ACETAMIDO-2-DEOXY-SN-GLYCEROL-3-PHOSPHOETHYLMETHYL SULFIDE, ... (4 entities in total) |
機能のキーワード | hydrolase |
由来する生物種 | Homo sapiens (human) |
細胞内の位置 | Membrane; Peripheral membrane protein: P14555 |
タンパク質・核酸の鎖数 | 6 |
化学式量合計 | 87389.50 |
構造登録者 | |
主引用文献 | Oh, B.H. A probe molecule composed of seventeen percent of total diffracting matter gives correct solutions in molecular replacement. Acta Crystallogr.,Sect.D, 51:140-144, 1995 Cited by PubMed Abstract: It is often found in the crystallization of enzyme-inhibitor complexes that an inhibitor causes crystal packing which is different to that of native protein. This is the case for crystals of human non-pancreatic secreted phospholipase A(2) (124 residues) containing six molecules in the asymmetric unit when the protein is complexed with a potential acylamino analogue of a phospholid. The hexameric structure was determined by molecular replacement using the structure of monomeric native protein as a probe. As an extension to the experiment, it was tested whether a backbone polypeptide composed of 17% of a known monomeric structure could find its correct position on a target molecule in molecular replacement. A probe model composed of the backbone atoms of the N-terminal 77 residues of lysine-, arginine-, ornithine-binding protein (LAO, a total of 238 residues) liganded with lysine correctly finds its position on LAO liganded with histidine which crystallizes as a monomer in the asymmetric unit. The results indicate that as little as 17% of total diffracting matter can be used in molecular replacement to solve crystal structures or to obtain phase information which can be combined with phases obtained by the isomorphous-replacement method. PubMed: 15299314DOI: 10.1107/S0907444994010024 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.57 Å) |
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