N-TERMINAL HIS-TAG IN PLACE OF THE NATIVE N-TERMINAL 33 AMINO ACIDS AND THE C-TERMINAL DOMAIN (OF ...N-TERMINAL HIS-TAG IN PLACE OF THE NATIVE N-TERMINAL 33 AMINO ACIDS AND THE C-TERMINAL DOMAIN (OF 353 RESIDUES) IS REMOVED LEAVING JUST THE C2 CACHE CHEMOSENSOR DOMAIN
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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: 3.53 Å3/Da / 溶媒含有率: 65.1 % / 解説: NONE
結晶化
温度: 293 K / 手法: 蒸気拡散法, シッティングドロップ法 / pH: 6.5 詳細: PROTEIN AT 8.5 MG/ML IN 50 MM BISTRIS CHLORIDE, PH 6.5, 50 MM SODIUM CHLORIDE IN EQUAL VOLUME WITH 27% PEG 4000 AND 3% SUCROSE AT 20 C IN SITTING DROP PLATES. CRYSTALS WERE LATER SOAKED IN ...詳細: PROTEIN AT 8.5 MG/ML IN 50 MM BISTRIS CHLORIDE, PH 6.5, 50 MM SODIUM CHLORIDE IN EQUAL VOLUME WITH 27% PEG 4000 AND 3% SUCROSE AT 20 C IN SITTING DROP PLATES. CRYSTALS WERE LATER SOAKED IN RESERVOIR SOLUTION WITH 40 MM NEUTRALIZED PROPIONATE.
解像度: 1.98→63.59 Å / Cor.coef. Fo:Fc: 0.97 / Cor.coef. Fo:Fc free: 0.962 / SU B: 3.109 / SU ML: 0.084 / 交差検証法: THROUGHOUT / ESU R: 0.112 / ESU R Free: 0.103 / 立体化学のターゲット値: MAXIMUM LIKELIHOOD 詳細: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS. U VALUES REFINED INDIVIDUALLY
Rfactor
反射数
%反射
Selection details
Rfree
0.17741
842
5.3 %
RANDOM
Rwork
0.15669
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obs
0.15785
15189
99.97 %
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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