THE PROTEIN USED FOR CRYSTALLIZATION CONTAINED AMINO-ACIDS AS GIVEN IN DBREF. THIS PROTEIN LIKELY ...THE PROTEIN USED FOR CRYSTALLIZATION CONTAINED AMINO-ACIDS AS GIVEN IN DBREF. THIS PROTEIN LIKELY DEGRADED TO A TRUNCATED SPECIES DURING THE CRYSTALLIZATION EXPERIMENT. THEREFORE, CALCULATED VM AND VS VALUES ARE BASED ON AN ESTIMATE. THE AUTHORS ASSUMED RESIDUES 161 TO 281 TO BE PRESENT.
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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: 2.06 Å3/Da / 溶媒含有率: 40.41 %
結晶化
温度: 292 K / 手法: 蒸気拡散法, シッティングドロップ法 / pH: 8 詳細: 0.2 M calcium chloride, 20 % PEG3350, pH 8.0, VAPOR DIFFUSION, SITTING DROP, temperature 292K
モノクロメーター: SINGLE SILICON (111) / プロトコル: SINGLE WAVELENGTH / 単色(M)・ラウエ(L): M / 散乱光タイプ: x-ray
放射波長
波長: 0.933 Å / 相対比: 1
反射
解像度: 2.1→50 Å / Num. obs: 23906 / % possible obs: 100 % / Observed criterion σ(I): -4 / 冗長度: 7.8 % / Biso Wilson estimate: 38.4 Å2 / Rmerge(I) obs: 0.102 / Net I/σ(I): 14.7
反射 シェル
解像度: 2.1→2.13 Å / 冗長度: 7.7 % / Rmerge(I) obs: 0.498 / Mean I/σ(I) obs: 3.2 / % possible all: 100
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解析
ソフトウェア
名称
バージョン
分類
DNA
データ収集
PHASER
位相決定
REFMAC
5.5.0102
精密化
HKL-2000
データ削減
SCALEPACK
データスケーリング
精密化
構造決定の手法: 分子置換 / 解像度: 2.2→50 Å / Cor.coef. Fo:Fc: 0.951 / Cor.coef. Fo:Fc free: 0.928 / SU B: 12.606 / SU ML: 0.145 / 交差検証法: THROUGHOUT / ESU R: 0.239 / ESU R Free: 0.202 / 立体化学のターゲット値: MAXIMUM LIKELIHOOD 詳細: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS THE PROTEIN USED FOR CRYSTALLIZATION CONTAINED AMINO-ACIDS AS GIVEN IN DBREF. THIS PROTEIN LIKELY DEGRADED TO A TRUNCATED SPECIES DURING THE ...詳細: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS THE PROTEIN USED FOR CRYSTALLIZATION CONTAINED AMINO-ACIDS AS GIVEN IN DBREF. THIS PROTEIN LIKELY DEGRADED TO A TRUNCATED SPECIES DURING THE CRYSTALLIZATION EXPERIMENT. THEREFORE, CALCULATED VM AND VS VALUES ARE BASED ON AN ESTIMATE. THE AUTHORS ASSUMED RESIDUES 161 TO 281 TO BE PRESENT.
Rfactor
反射数
%反射
Selection details
Rfree
0.245
1056
5.1 %
RANDOM
Rwork
0.195
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obs
0.198
19600
100 %
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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: BABINET MODEL WITH MASK