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1ABS

PHOTOLYSED CARBONMONOXY-MYOGLOBIN AT 20 K

Experimental procedure
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X12C
Synchrotron siteNSLS
BeamlineX12C
Temperature [K]20
Detector technologyIMAGE PLATE AREA DETECTOR
Collection date1994-03
DetectorMARRESEARCH
Spacegroup nameP 6
Unit cell lengths90.420, 90.420, 45.400
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution7.000 - 1.500
R-factor0.207
Rwork0.207
Structure solution methodDIFFERENCE FOURIER
Starting model (for MR)2mgk
RMSD bond length0.010
RMSD bond angle1.700
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR (3.1)
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]9999.000

*

1.700
High resolution limit [Å]1.5001.500
Rmerge0.063
Total number of observations93946

*

Number of reflections30947
Completeness [%]90.078
Redundancy3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Batch method

*

9PROTEIN WAS CRYSTALLIZED FROM 3.6 M AMMONIUM SULFATE. CRYSTALS WER SOAKED FOR 1 HOUR IN A THOROUGHLY DEGASSED AND N2 - SATURATED CRYOPROTECTANT SOLUTION MADE BY ADDITION OF 100 MG SUCROSE, 100 MG GLUCOSE AND 8 MG NA-DITHIONATE TO 1 ML OF 70% SATURATED AMMONIUM SULFATE WITH 50 MM TRIS. HCL PH 9.0. THEN THE SOLUTION WAS EXCHANGED AGAINST A CO SATURATED ONE. DISTINCT COLOR CHANGES ACCOMPANIED THE FORMATION OF UNLIGATED MYOGLOBIN FROM MET-MB AND MBCO FROM UNLIGATED MB.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
111protein70 (mg/ml)
211ammonium sulfate2.2-2.6 (M)
311Tris-HCl20 (mM)
411EDTA1 (mM)

218853

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