SEQUENCE THIS CONSTRUCT WAS EXPRESSED WITH A PURIFICATION TAG MGSDKIHHHHHHENLYFQG. THE TAG WAS ...SEQUENCE THIS CONSTRUCT WAS EXPRESSED WITH A PURIFICATION TAG MGSDKIHHHHHHENLYFQG. THE TAG WAS REMOVED WITH TEV PROTEASE LEAVING ONLY A GLYCINE (0) FOLLOWED BY THE TARGET SEQUENCE.
解像度: 2.5→29.591 Å / Num. obs: 17799 / % possible obs: 99.9 % / 冗長度: 7.2 % / Biso Wilson estimate: 60.865 Å2 / Rmerge(I) obs: 0.084 / Rsym value: 0.084 / Net I/σ(I): 16.8
反射 シェル
Diffraction-ID: 1
解像度 (Å)
冗長度 (%)
Rmerge(I) obs
Mean I/σ(I) obs
Num. measured all
Num. unique all
Rsym value
% possible all
2.5-2.56
7.3
0.806
2.4
9445
1288
0.806
100
2.56-2.64
7.4
0.641
3.1
9165
1246
0.641
100
2.64-2.71
7.3
0.555
3.5
8999
1226
0.555
100
2.71-2.8
7.3
0.446
4.3
8701
1187
0.446
100
2.8-2.89
7.3
0.325
5.9
8436
1156
0.325
100
2.89-2.99
7.3
0.273
7
8285
1133
0.273
100
2.99-3.1
7.3
0.218
8.9
7836
1069
0.218
100
3.1-3.23
7.3
0.16
11.9
7569
1039
0.16
100
3.23-3.37
7.3
0.132
14.4
7278
1002
0.132
100
3.37-3.54
7.3
0.104
18.1
7067
973
0.104
100
3.54-3.73
7.2
0.078
23.8
6642
919
0.078
100
3.73-3.95
7.2
0.069
26.7
6229
867
0.069
100
3.95-4.23
7.2
0.063
31.4
5967
833
0.063
100
4.23-4.56
7.2
0.053
36.1
5479
766
0.053
100
4.56-5
7.1
0.05
39.1
5055
712
0.05
100
5-5.59
7
0.052
36.8
4578
658
0.052
100
5.59-6.45
6.8
0.063
34.1
4007
586
0.063
100
6.45-7.91
6.5
0.064
35.8
3285
509
0.064
100
7.91-11.18
6.3
0.045
42.2
2503
398
0.045
100
11.18-29.59
5.7
0.043
39.3
1316
232
0.043
93.9
-
位相決定
位相決定
手法: 多波長異常分散
-
解析
ソフトウェア
名称
バージョン
分類
NB
REFMAC
5.2.0019
精密化
PHENIX
精密化
SHELX
位相決定
MolProbity
3beta29
モデル構築
SCALA
3.2.5
データスケーリング
PDB_EXTRACT
3.006
データ抽出
MOSFLM
データ削減
autoSHARP
位相決定
精密化
構造決定の手法: 多波長異常分散 / 解像度: 2.5→29.591 Å / Cor.coef. Fo:Fc: 0.934 / Cor.coef. Fo:Fc free: 0.914 / Occupancy max: 1 / Occupancy min: 0.37 / SU B: 23.429 / SU ML: 0.233 / TLS residual ADP flag: LIKELY RESIDUAL / 交差検証法: THROUGHOUT / σ(F): 0 / ESU R: 0.635 / ESU R Free: 0.296 立体化学のターゲット値: MAXIMUM LIKELIHOOD WITH PHASES 詳細: 1. HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS. 2. ATOM RECORDS CONTAIN RESIDUAL B FACTORS ONLY. 3. A MET-INHIBITION PROTOCOL WAS USED FOR SELENOMETHIONINE INCORPORATION DURING PROTEIN ...詳細: 1. HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS. 2. ATOM RECORDS CONTAIN RESIDUAL B FACTORS ONLY. 3. A MET-INHIBITION PROTOCOL WAS USED FOR SELENOMETHIONINE INCORPORATION DURING PROTEIN EXPRESSION. THE OCCUPANCY OF THE SE ATOMS IN THE MSE RESIDUES WAS REDUCED TO 0.75 FOR THE REDUCED SCATTERING POWER DUE TO PARTIAL S-MET INCORPORATION.
Rfactor
反射数
%反射
Selection details
Rfree
0.257
903
5.1 %
RANDOM
Rwork
0.237
-
-
-
obs
0.238
17760
99.89 %
-
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: BABINET MODEL WITH MASK