AUTHORS STATE THAT THE RESIDUES AT POSITION 110, 111, AND 130 ARE CORRECTLY IDENTIFIED AND THE ...AUTHORS STATE THAT THE RESIDUES AT POSITION 110, 111, AND 130 ARE CORRECTLY IDENTIFIED AND THE BIOCHEMICAL DATA SHOWS THAT THE PROTEIN IS ACTIVE.
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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: 2.6 Å3/Da / 溶媒含有率: 52.7 %
結晶化
温度: 293 K / pH: 5.5 詳細: 100mM Na-acetate pH 4.25-5.5, 10mM CaCl2 or CaAc2, 4-8% (w/v) of PEG8000, VAPOR DIFFUSION, temperature 293K
解像度: 2.35→55.556 Å / Cor.coef. Fo:Fc: 0.901 / Cor.coef. Fo:Fc free: 0.866 / Occupancy max: 1 / Occupancy min: 0.5 / SU B: 19.258 / SU ML: 0.209 / SU R Cruickshank DPI: 0.576 / 交差検証法: THROUGHOUT / ESU R: 0.561 / ESU R Free: 0.324 / 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
0.29343
3156
10.2 %
RANDOM
Rwork
0.2403
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obs
0.2457
27769
91.58 %
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all
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34081
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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: 1.4 Å / 溶媒モデル: MASK