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3S67

Crystal structure of V57P mutant of human cystatin C

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-BM
Synchrotron siteAPS
Beamline19-BM
Temperature [K]100
Detector technologyCCD
Collection date2010-07-09
DetectorADSC QUANTUM 210r
Wavelength(s)0.97923
Spacegroup nameI 4 3 2
Unit cell lengths140.135, 140.135, 140.135
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution27.480 - 2.260
R-factor0.18869
Rwork0.187
R-free0.22890
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1g96
RMSD bond length0.016
RMSD bond angle1.657
Data reduction softwareHKL-3000
Data scaling softwareHKL-3000
Phasing softwareMOLREP
Refinement softwareREFMAC (5.5.0102)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.300
High resolution limit [Å]2.2602.260
Rmerge0.088
Number of reflections11234
<I/σ(I)>36.52.16
Completeness [%]99.8
Redundancy1412.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.52930.1M Imidazole pH=6.5 0.9M Sodium acetate, additive 2.0M NDSB-221, VAPOR DIFFUSION, HANGING DROP, temperature 293K

219869

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