THE CONSTRUCT WAS EXPRESSED WITH A PURIFICATION TAG MGSDKIHHHHHHENLYFQG. THE TAG WAS REMOVED WITH ...THE 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: 2.05→29.961 Å / Num. obs: 79699 / % possible obs: 99.8 % / 冗長度: 3.7 % / Biso Wilson estimate: 24.029 Å2 / Rmerge(I) obs: 0.143 / Rsym value: 0.143 / Net I/σ(I): 8.1
反射 シェル
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
2.05-2.1
3.7
0.804
1.6
21973
5863
0.804
100
2.1-2.16
3.7
0.715
1.8
21319
5691
0.715
100
2.16-2.22
3.8
0.606
2.2
20825
5547
0.606
100
2.22-2.29
3.8
0.53
2.5
20164
5372
0.53
100
2.29-2.37
3.8
0.463
2.9
19699
5239
0.463
100
2.37-2.45
3.8
0.416
3.2
18992
5054
0.416
100
2.45-2.54
3.8
0.349
3.9
18225
4849
0.349
100
2.54-2.65
3.8
0.298
4.5
17752
4726
0.298
100
2.65-2.76
3.8
0.24
5.4
17022
4533
0.24
100
2.76-2.9
3.8
0.186
6.8
16201
4312
0.186
100
2.9-3.06
3.8
0.139
9
15491
4119
0.139
100
3.06-3.24
3.8
0.105
11.2
14588
3888
0.105
99.9
3.24-3.47
3.8
0.082
14
13834
3686
0.082
99.9
3.47-3.74
3.7
0.07
16.5
12884
3438
0.07
99.9
3.74-4.1
3.7
0.056
19.7
11851
3163
0.056
99.8
4.1-4.58
3.7
0.05
22.1
10674
2869
0.05
99.7
4.58-5.29
3.7
0.054
22
9486
2541
0.054
99.5
5.29-6.48
3.7
0.057
19.8
7979
2163
0.057
99.1
6.48-9.17
3.6
0.046
21.3
6207
1704
0.046
98.9
9.17-29.96
3.5
0.038
25.4
3273
942
0.038
95.3
-
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
5.5.0110
精密化
PHENIX
精密化
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
HELXD
位相決定
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: 2.05→29.961 Å / Cor.coef. Fo:Fc: 0.953 / Cor.coef. Fo:Fc free: 0.92 / Occupancy max: 1 / Occupancy min: 0.2 / SU B: 9.491 / SU ML: 0.133 / 交差検証法: THROUGHOUT / σ(F): 0 / ESU R Free: 0.181 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 RECORD CONTAINS SUM OF TLS AND RESIDUAL B FACTORS. ANISOU RECORD CONTAINS SUM OF TLS AND RESIDUAL U FACTORS. WATERS WERE EXCLUDED ...詳細: 1.HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS. 2.ATOM RECORD CONTAINS SUM OF TLS AND RESIDUAL B FACTORS. ANISOU RECORD CONTAINS SUM OF TLS AND RESIDUAL U FACTORS. WATERS WERE EXCLUDED FROM AUTOMATIC TLS ASSIGNMENT. 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 TO ACCOUNT FOR THE REDUCED SCATTERING POWER DUE TO PARTIAL S-MET INCORPORATION. 4.AN UNKNOWN LIGAND HAS BEEN MODELED IN THE STRUCTURE. BASED ON DENSITY AND HYDROGEN BONDING DONOR/ACCEPTOR LOCATIONS, THIS MAY BE NITROBENZENE, BENZOATE, OR NICOTINIC ACID. 5. SODIUM (NA) IONS AND CITRATE (FLC) ANIONS FROM THE CRYSTALLIZATION REAGENT, IMIDAZOLE (IMD) FROM THE PROTEIN BUFFER AND ETHYLENE GLYCOL (EDO) FROM THE CRYOPROTECTANT SOLUTION ARE MODELED IN THE STRUCTURE.
Rfactor
反射数
%反射
Selection details
Rfree
0.24
3987
5 %
RANDOM
Rwork
0.184
-
-
-
obs
0.187
79629
99.71 %
-
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