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1CB7

GLUTAMATE MUTASE FROM CLOSTRIDIUM COCHLEARIUM RECONSTITUTED WITH METHYL-COBALAMIN

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE X11
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineX11
Temperature [K]105
Detector technologyIMAGE PLATE
Collection date1998-10-01
DetectorMARRESEARCH
Spacegroup nameP 1 21 1
Unit cell lengths64.330, 113.140, 108.610
Unit cell angles90.00, 95.62, 90.00
Refinement procedure
Resolution25.000 - 2.000
R-factor0.1597
R-free0.21850
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)GLUTAMATE MUTASE RECONSTITUTED WITH CYANOCOBALAMIN
RMSD bond length0.005
RMSD bond angle24.000

*

Data reduction softwareDENZO
Data scaling softwareCCP4 ((SCALA))
Phasing softwareX-PLOR
Refinement softwareSHELXL-97
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]25.0002.110
High resolution limit [Å]2.0002.000
Rmerge0.076

*

0.189

*

Total number of observations258385

*

Number of reflections100016
<I/σ(I)>5.61.3
Completeness [%]96.196.2
Redundancy2.62.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

7.5

*

pH 4.5
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111PEG 4000
211sodium tartarate
311METHYL COBALAMIN
411CdCl2
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein3.5 (mg/ml)
21drop2 (mM)
31drop(2S,4S)-45-fluoroglutamate5 (mM)
41dropB12(cyano-or-methylcobalamin)2.5 (mg/ml)
51dropNa cacodylate10 (mM)
61reservoirPEG40006 (%(w/v))
71reservoirDL-tartaric acid100 (M)

222415

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