BIOMOLECULE: 1 THIS ENTRY CONTAINS THE CRYSTALLOGRAPHIC ASYMMETRIC UNIT WHICH CONSISTS OF 2 CHAIN(S) ...BIOMOLECULE: 1 THIS ENTRY CONTAINS THE CRYSTALLOGRAPHIC ASYMMETRIC UNIT WHICH CONSISTS OF 2 CHAIN(S). SEE REMARK 350 FOR INFORMATION ON GENERATING THE BIOLOGICAL MOLECULE(S). SIZE EXCLUSION CHROMATOGRAPHY WITH STATIC LIGHT SCATTERING SUPPORTS THE ASSIGNMENT OF THE DIMER AS A SIGNIFICANT OLIGOMERIZATION STATE.
Remark 999
SEQUENCE THE CONSTRUCT WAS EXPRESSED WITH A PURIFICATION TAG MGSDKIHHHHHHENLYFQG. THE TAG WAS ...SEQUENCE THE CONSTRUCT WAS EXPRESSED WITH A PURIFICATION TAG MGSDKIHHHHHHENLYFQG. THE TAG WAS REMOVED WITH TEV PROTEASE LEAVING ONLY A GLYCINE FOLLOWED BY THE TARGET SEQUENCE.
解像度: 1.5→86.066 Å / Num. obs: 35176 / % possible obs: 76.7 % / 冗長度: 2.9 % / Rmerge(I) obs: 0.05 / Rsym value: 0.05 / Net I/σ(I): 9.4
反射 シェル
Diffraction-ID: 2
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
1.5-1.54
2.7
0.183
4.1
5577
2100
0.183
61.3
1.54-1.58
2.7
0.153
4.8
5683
2129
0.153
64.9
1.58-1.63
2.7
0.134
5.5
5748
2126
0.134
65.5
1.63-1.68
2.7
0.112
6.2
5739
2113
0.112
67.4
1.68-1.73
2.8
0.105
7.2
5794
2085
0.105
70.4
1.73-1.79
2.8
0.093
8
5922
2115
0.093
72.6
1.79-1.86
2.8
0.079
9.4
6046
2122
0.079
74
1.86-1.94
3
0.07
10.4
6077
2052
0.07
75.3
1.94-2.02
3
0.063
11.4
6034
1985
0.063
75.5
2.02-2.12
3.2
0.056
12.8
6181
1958
0.056
79.8
2.12-2.24
3.2
0.057
12.2
6149
1944
0.057
81.9
2.24-2.37
3.1
0.059
11.7
5822
1876
0.059
83.7
2.37-2.54
3.1
0.056
12.3
5520
1799
0.056
85.8
2.54-2.74
3
0.048
14.1
5181
1715
0.048
86.5
2.74-3
3
0.044
15.7
4863
1616
0.044
89.4
3-3.35
3
0.046
14.1
4421
1480
0.046
92.1
3.35-3.87
2.9
0.042
15.6
3989
1357
0.042
92.7
3.87-4.74
3
0.037
16.7
3517
1174
0.037
97.3
4.74-6.71
3.2
0.041
16.5
2908
913
0.041
96.9
6.71-86.07
4.3
0.045
14.9
2237
517
0.045
99
-
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
SHELX
精密化
MolProbity
3beta29
モデル構築
SOLVE
位相決定
SCALA
データスケーリング
PDB_EXTRACT
2
データ抽出
MAR345
CCD
データ収集
MOSFLM
データ削減
SHELXL-97
精密化
精密化
構造決定の手法: 多波長異常分散 / 解像度: 1.5→28.736 Å / Num. parameters: 6902 / Num. restraintsaints: 9250 / 交差検証法: FREE R / 立体化学のターゲット値: ENGH AND HUBER 詳細: 1. HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS. 2. A MET-INHIBITION PROTOCOL WAS USED FOR SELENOMETHIONINE INCORPORATION DURING PROTEIN EXPRESSION. THE OCCUPANCY OF THE SE ATOMS IN THE ...詳細: 1. HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS. 2. 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. 3. DATA IS TETARTOHEDRALLY TWINNED. REFINEMENT WAS PERFORMED WITH THE TWIN OPERATORS (K,H,-L), (-K,-H,-L), AND (-H,-K,L) AND THE RESPECTIVE TWIN FRACTIONS OF 0.28, 0.19, 0.15. 4. THE NOMINAL RESOLUTION IS 1.65 A WITH 7312 OBSERVED REFLECTIONS BETWEEN 1.65-1.50 (64.2% COMPLETE FOR THIS SHELL) INCLUDED IN THE REFINEMENT. 5. THE R-FREE SET WAS GENERATED USING THE TWIN LAWS.