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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
Unit cell lengths222.800, 222.800, 222.800
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 3.000
R-factor0.205
Rwork0.205
R-free0.24900
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1eaa
RMSD bond length0.010
RMSD bond angle24.700

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Data reduction softwareMOSFLM
Data scaling softwareCCP4 ((ROTAVATA)
Phasing softwareX-PLOR (3.851)
Refinement softwareX-PLOR (3.851)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0003.160
High resolution limit [Å]3.0003.000
Rmerge0.046

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0.145

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Number of reflections9906
<I/σ(I)>134.9
Completeness [%]98.5100
Redundancy4.14.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
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
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein20 (mg/ml)
21droppotassium phosphate50 (mM)
31dropdithiothreitol1 (mM)
41dropEDTA1 (mM)
51dropbenzamidine1 (mM)
61reservoirammonium sulfate1.2 (M)
71reservoirethanol1 (%(v/v))

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數據於2024-04-24公開中

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