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1E9I

Enolase from E.coli

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsELETTRA BEAMLINE 5.2R
Synchrotron siteELETTRA
Beamline5.2R
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1999-02-15
DetectorMAR scanner 345 mm plate
Spacegroup nameC 1 2 1
Unit cell lengths107.883, 150.006, 127.411
Unit cell angles90.00, 109.18, 90.00
Refinement procedure
Resolution27.970 - 2.480
R-factor0.229
Rwork0.229
R-free0.27600
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ebg
RMSD bond length0.007
RMSD bond angle22.000

*

Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareCNS (0.9)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]27.9702.560
High resolution limit [Å]2.4802.470
Rmerge0.0530.107
Number of reflections636646458

*

<I/σ(I)>3310
Completeness [%]98.390
Redundancy44
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, sitting drop

*

720

*

20% PEG3350, 0.2M MG ACETATE, pH 7.00
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropenolase35 (mg/ml)
21dropPEG335010 (%(w/v))
31dropmagnesium acetate100 (mM)
41reservoirPEG335020 (%)
51reservoirmagnesium acetate200 (mM)

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