- PDB-2ook: Crystal structure of a protein with unknown function (YP_749275.1... -
+
データを開く
IDまたはキーワード:
読み込み中...
-
基本情報
登録情報
データベース: PDB / ID: 2ook
タイトル
Crystal structure of a protein with unknown function (YP_749275.1) from Shewanella Frigidimarina NCIMB 400 at 1.80 A resolution
要素
Hypothetical protein
キーワード
STRUCTURAL GENOMICS / UNKNOWN FUNCTION / YP_749275.1 / hypothetical protein / Joint Center for Structural Genomics / JCSG / Protein Structure Initiative / PSI-2
BIOMOLECULE: 1 THIS ENTRY CONTAINS THE CRYSTALLOGRAPHIC ASYMMETRIC UNIT WHICH CONSISTS OF 2 CHAINS. ... BIOMOLECULE: 1 THIS ENTRY CONTAINS THE CRYSTALLOGRAPHIC ASYMMETRIC UNIT WHICH CONSISTS OF 2 CHAINS. SEE REMARK 350 FOR INFORMATION ON GENERATING THE BIOLOGICAL MOLECULE(S). SIZE EXCLUSION CHROMATOGRAPHY WITH STATIC LIGHT SCATTERING SUPPORTS THE ASSIGNMENT OF A DIMER AS THE 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 (0) FOLLOWED BY THE TARGET SEQUENCE.
モノクロメーター: Single crystal Si(111) bent (horizontal focusing) プロトコル: MAD / 単色(M)・ラウエ(L): M / 散乱光タイプ: x-ray
放射波長
ID
波長 (Å)
相対比
1
0.91837
1
2
0.9791
1
3
0.97879
1
反射
解像度: 1.8→28.571 Å / Num. obs: 22625 / % possible obs: 96.5 % / 冗長度: 3.8 % / Biso Wilson estimate: 24.85 Å2 / Rmerge(I) obs: 0.056 / Rsym value: 0.056 / Net I/σ(I): 13.6
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
1.8-1.85
3.8
0.653
2.1
6294
1640
0.653
95.3
1.85-1.9
3.8
0.514
1.5
6128
1597
0.514
95.5
1.9-1.95
3.8
0.407
1.9
5975
1570
0.407
96
1.95-2.01
3.8
0.294
2.6
5762
1507
0.294
95.7
2.01-2.08
3.8
0.226
3.3
5674
1487
0.226
96.3
2.08-2.15
3.8
0.184
4.2
5509
1436
0.184
96.2
2.15-2.23
3.8
0.146
5.3
5297
1379
0.146
96.2
2.23-2.32
3.8
0.126
5.9
5006
1315
0.126
96.5
2.32-2.43
3.8
0.105
7.1
4939
1292
0.105
96.8
2.43-2.55
3.8
0.092
8
4697
1232
0.092
96.6
2.55-2.68
3.8
0.075
9.2
4522
1188
0.075
96.9
2.68-2.85
3.8
0.063
11.3
4219
1104
0.063
97.1
2.85-3.04
3.8
0.051
13.6
4007
1054
0.051
97.5
3.04-3.29
3.8
0.038
17
3732
984
0.038
97.1
3.29-3.6
3.8
0.035
17.3
3375
891
0.035
97.5
3.6-4.02
3.8
0.031
20.4
3155
839
0.031
97.6
4.02-4.65
3.7
0.028
22.9
2686
722
0.028
97.9
4.65-5.69
3.7
0.03
19.8
2340
632
0.03
98
5.69-8.05
3.6
0.035
18.4
1771
492
0.035
98.4
8.05-28.57
3.4
0.029
23
908
264
0.029
93.5
-
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
MolProbity
3beta29
モデル構築
SHELX
位相決定
REFMAC
5.2.0019
精密化
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
CCP4
(SCALA)
データスケーリング
SHELXD
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: 1.8→28.571 Å / Cor.coef. Fo:Fc: 0.964 / Cor.coef. Fo:Fc free: 0.939 / SU B: 6.712 / SU ML: 0.106 / TLS residual ADP flag: LIKELY RESIDUAL / 交差検証法: THROUGHOUT / σ(F): 0 / ESU R: 0.146 / ESU R Free: 0.141 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. 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 FOR THE REDUCED SCATTERING POWER DUE TO PARTIAL S-MET INCORPORATION. 3. RESIDUES 1 IN CHAIN A AND 1-2, 80-81 IN CHAIN B ARE DISORDERED AND NOT INCLUDED IN THE MODEL. 4. EDO MOLECULES FROM THE CRYO SOLUTION ARE MODELED. 5. ATOM RECORDS CONTAIN RESIDUAL B FACTORS ONLY.
Rfactor
反射数
%反射
Selection details
Rfree
0.233
1162
5.1 %
RANDOM
Rwork
0.183
-
-
-
all
0.186
-
-
-
obs
0.186
22625
96.02 %
-
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