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6PM7

The structure of the triclinic crystal form of beef liver catalase at 1.85 A resolution

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 8.3.1
Synchrotron siteALS
Beamline8.3.1
Temperature [K]173
Detector technologyPIXEL
Collection date2018-09-20
DetectorDECTRIS PILATUS 300K
Wavelength(s)1.0
Spacegroup nameP 32 2 1
Unit cell lengths140.865, 140.865, 101.840
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution121.990 - 1.850
R-factor0.19363
Rwork0.192
R-free0.23248
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.006
RMSD bond angle1.391
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwarePHASER
Refinement softwareREFMAC (5.8.0238)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]122.0001.880
High resolution limit [Å]1.8501.850
Rmerge0.1422.590
Rmeas0.1452.910
Rpim0.0331.010
Number of reflections979874349
<I/σ(I)>9.80.3
Completeness [%]98.789.4
Redundancy17.47.9
CC(1/2)0.9980.501
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP6.5298Vapor diffusion with 10 ul drops and 0.6 ml reservoirs. Reservoirs were 6% PEG 3350 buffered with 0.1 M MES at pH 6.5. Drops were equal amounts of 35 mg/ml protein in H2O and reservoir solution. Growth time about two weeks.

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