マシュー密度: 2.05 Å3/Da / 溶媒含有率: 40.05 % 解説: THE STRUCTURE WAS SOLVED BY THE METHOD OF ITERATIVE SINGLE ANOMALOUS SCATTERING (B.C. WANG, (1985), METHODS ENZYMOL., 114, P90-117).
解像度: 2→40 Å / Num. obs: 3107 / % possible obs: 82.4 % / Observed criterion σ(I): 2 / Biso Wilson estimate: 19.3 Å2 / Rsym value: 0.066
反射
*PLUS
Rmerge(I) obs: 0.066
反射 シェル
*PLUS
% possible obs: 54.9 %
-
解析
ソフトウェア
名称
バージョン
分類
X-PLOR
3.843
モデル構築
X-PLOR
3.843
精密化
R-AXIS
データ削減
R-AXIS
データスケーリング
X-PLOR
3.843
位相決定
精密化
構造決定の手法: 分子置換 開始モデル: THE STARTING STRUCTURAL MODEL WAS DETERMINED FROM A CRYSTAL GROWN WITH THE RECOMBINANT, SINGLY-IODINATED PROTEIN, ISOFORM HPLC-6. THIS MODEL IS NOT YET AVAILABLE. 解像度: 2→40 Å / Rfactor Rfree error: 0.016 / Data cutoff high absF: 10000000 / Data cutoff low absF: 0.001 / Isotropic thermal model: RESTRAINED / 交差検証法: THROUGHOUT / σ(F): 2 / 詳細: BULK ENT MODEL USED
Rfactor
反射数
%反射
Selection details
Rfree
0.259
304
9.8 %
RANDOM
Rwork
0.204
-
-
-
obs
0.204
3107
82.6 %
-
原子変位パラメータ
Biso mean: 17.4 Å2
Refine analyze
Free
Obs
Luzzati coordinate error
0.33 Å
0.26 Å
Luzzati d res low
-
40 Å
Luzzati sigma a
0.29 Å
0.26 Å
精密化ステップ
サイクル: LAST / 解像度: 2→40 Å
タンパク質
核酸
リガンド
溶媒
全体
原子数
445
0
0
33
478
拘束条件
Refine-ID
タイプ
Dev ideal
Dev ideal target
X-RAY DIFFRACTION
x_bond_d
0.014
X-RAY DIFFRACTION
x_bond_d_na
X-RAY DIFFRACTION
x_bond_d_prot
X-RAY DIFFRACTION
x_angle_d
X-RAY DIFFRACTION
x_angle_d_na
X-RAY DIFFRACTION
x_angle_d_prot
X-RAY DIFFRACTION
x_angle_deg
1.7
X-RAY DIFFRACTION
x_angle_deg_na
X-RAY DIFFRACTION
x_angle_deg_prot
X-RAY DIFFRACTION
x_dihedral_angle_d
27.2
X-RAY DIFFRACTION
x_dihedral_angle_d_na
X-RAY DIFFRACTION
x_dihedral_angle_d_prot
X-RAY DIFFRACTION
x_improper_angle_d
1.71
X-RAY DIFFRACTION
x_improper_angle_d_na
X-RAY DIFFRACTION
x_improper_angle_d_prot
X-RAY DIFFRACTION
x_mcbond_it
2.97
1.5
X-RAY DIFFRACTION
x_mcangle_it
3.86
2
X-RAY DIFFRACTION
x_scbond_it
4.9
2
X-RAY DIFFRACTION
x_scangle_it
6.15
2.5
LS精密化 シェル
解像度: 2→2.07 Å / Rfactor Rfree error: 0.06 / Total num. of bins used: 10