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8QVO

L211Q, L254N, T262G mutant of carboxypeptidase T from Thermoactinomyces vulgaris

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsKURCHATOV SNC BEAMLINE K4.4
Synchrotron siteKURCHATOV SNC
BeamlineK4.4
Temperature [K]100
Detector technologyCCD
Collection date2023-10-02
DetectorMAR CCD 130 mm
Wavelength(s)0.752680
Spacegroup nameP 63 2 2
Unit cell lengths158.085, 158.085, 104.589
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution28.910 - 1.960
R-factor0.14649
Rwork0.146
R-free0.16550
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.013
RMSD bond angle1.774
Data reduction softwareiMOSFLM
Data scaling softwareSCALA
Phasing softwarePHASER
Refinement softwareREFMAC (5.8.0267)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.070
High resolution limit [Å]1.9601.960
Rmerge0.1100.360
Rmeas0.1150.376
Number of reflections11035715903
<I/σ(I)>5.87572.05
Completeness [%]100.099.99
Redundancy12.099.41
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP2931.4 SA

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