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1EBL

THE 1.8 A CRYSTAL STRUCTURE AND ACTIVE SITE ARCHITECTURE OF BETA-KETOACYL-[ACYL CARRIER PROTEIN] SYNTHASE III (FABH) FROM ESCHERICHIA COLI

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsCHESS BEAMLINE F2
Synchrotron siteCHESS
BeamlineF2
Temperature [K]100
Detector technologyCCD
Collection date1999-01-21
DetectorOTHER
Spacegroup nameP 21 21 21
Unit cell lengths63.130, 64.300, 165.920
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 1.800
R-factor0.189
Rwork0.187
R-free0.22500
RMSD bond length0.011
RMSD bond angle1.800
Data reduction softwareMOSFLM
Data scaling softwareCCP4 ((SCALA))
Phasing softwareMLPHARE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]31.6001.890
High resolution limit [Å]1.8001.800
Rmerge0.0560.140
Total number of observations230489

*

Number of reflections61752
<I/σ(I)>20.52
Completeness [%]97.489.8
Redundancy3.732.88
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.4

*

2981.8-2.0 M ammonium sulphate, 2% PEG 400, 0.1M HEPES, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 298.0K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein15 (mg/ml)
21dropTris-HCl20 (mM)
31dropEDTA1 (mM)
41dropdithiothreitol1 (mM)
51reservoirammonium sulfate1.8-2.0 (M)
61reservoirPEG4002 (%)
71reservoirHEPES100 (mM)

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건을2024-04-17부터공개중

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