THE X-RAY STRUCTURE REVEALS THAT NAMI-A BINDS THE PROTEIN, AS NAKED RUTHENIUM ION, AT TWO DISTINCT ...THE X-RAY STRUCTURE REVEALS THAT NAMI-A BINDS THE PROTEIN, AS NAKED RUTHENIUM ION, AT TWO DISTINCT SITES (EITHER TO ASP101 OR TO ASP119), AFTER RELEASING ALL ITS ORIGINAL LIGANDS (DMSO, IMIDAZOLE AND CL-). THIS INDICATES THAT NAMI-A UNDERGOES DRAMATIC CHANGES IN THE COORDINATION ENVIRONMENT OF THE RUTHENIUM CENTRE UPON THE PROTEIN BINDING AND THAT ASP SIDE CHAINS ARE PREFERENTIAL TARGET SITES FOR RUTHENIUM BINDING TO THE PROTEIN
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実験情報
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実験
実験
手法: X線回折 / 使用した結晶の数: 1
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試料調製
結晶
マシュー密度: 1.97 Å3/Da / 溶媒含有率: 37.52 %
結晶化
温度: 293 K / 手法: 蒸気拡散法, ハンギングドロップ法 / pH: 4.5 詳細: Crystals of the HEWL/NAMI-A adduct suitable for X-ray diffraction studies Have been grown by hanging drop vapor diffusion by mixing 1 L of 20 mg/mL HEWL/NAMI-A complex (protein to metal ratio ...詳細: Crystals of the HEWL/NAMI-A adduct suitable for X-ray diffraction studies Have been grown by hanging drop vapor diffusion by mixing 1 L of 20 mg/mL HEWL/NAMI-A complex (protein to metal ratio 1:10) with an equal volume of reservoir solution containing 1.0 M NaCl and 50 mM sodium acetate pH 4.5. These crystals were fished with nylon loops and flash-frozen at 100 K using nitrogen gas, without cryoprotectant. This procedure partly dehydrates the crystals, enhancing in some cases the resolution of X-ray diffraction data, VAPOR DIFFUSION, HANGING DROP, temperature 293K
解像度: 1.85→22.15 Å / Cor.coef. Fo:Fc: 0.955 / Cor.coef. Fo:Fc free: 0.936 / SU B: 3.321 / SU ML: 0.102 / 交差検証法: THROUGHOUT / ESU R: 0.163 / ESU R Free: 0.159 / 立体化学のターゲット値: MAXIMUM LIKELIHOOD / 詳細: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
Rfactor
反射数
%反射
Selection details
Rfree
0.23994
490
4.8 %
RANDOM
Rwork
0.17626
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obs
0.17933
9628
98.91 %
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溶媒の処理
イオンプローブ半径: 0.8 Å / 減衰半径: 0.8 Å / VDWプローブ半径: 1.2 Å / 溶媒モデル: MASK