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1E2O

CATALYTIC DOMAIN FROM DIHYDROLIPOAMIDE SUCCINYLTRANSFERASE

Experimental procedure
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL7-1
Synchrotron siteSSRL
BeamlineBL7-1
Temperature [K]298
Detector technologyIMAGE PLATE
Collection date1994-03
DetectorMARRESEARCH
Spacegroup nameF 4 3 2
格子定数 [Å]222.800, 222.800, 222.800
格子定数 [度]90.00, 90.00, 90.00
精密化法
残基20.000 - 3.000
R因子0.205
Rwork0.205
R-free0.24900
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1eaa
結合長の平均二乗偏差(RMSD) [Å]0.010
結合角の平均二乗偏差(RMSD) [度]24.700

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Data reduction softwareMOSFLM
Data scaling softwareCCP4 ((ROTAVATA)
Phasing softwareX-PLOR (3.851)
Refinement softwareX-PLOR (3.851)
Quality characteristics
 OverallOuter shell
分解能 [Å] (低)20.0003.160
分解能 [Å] (高)3.0003.000
Rmerge_l_obs0.046

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0.145

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独立反射数9906
<I/σ(I)>134.9
完全性 [%]98.5100
冗長性4.14.5
結晶化条件
結晶ID方法pH温度溶液条件
1Vapor diffusion, hanging drop

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7.3

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PROTEIN WAS CRYSTALLIZED FROM 1.2M AMMONIUM SULFATE, 1% ETHANOL, 50 MM POTASSIUM PHOSPHATE, PH 7.0
文献の結晶化試薬
ID結晶ID溶液試薬名濃度 (単位) (単位)詳細
11dropprotein20 (mg/ml)
21droppotassium phosphate50 (mM)
31dropdithiothreitol1 (mM)
41dropEDTA1 (mM)
51dropbenzamidine1 (mM)
61reservoirammonium sulfate1.2 (M)
71reservoirethanol1 (%(v/v))

217705

件を2024-03-27に公開中

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