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7T7N

Structure of SPCC1393.13 protein from fission yeast

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 24-ID-C
Synchrotron siteAPS
Beamline24-ID-C
Temperature [K]100
Detector technologyPIXEL
Collection date2021-10-23
DetectorDECTRIS EIGER2 X 16M
Wavelength(s)1.5895
Spacegroup nameC 1 2 1
Unit cell lengths124.720, 88.221, 48.257
Unit cell angles90.00, 101.07, 90.00
Refinement procedure
Resolution47.360 - 2.000
R-factor0.1621
Rwork0.160
R-free0.20030
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)7t7k
RMSD bond length0.008
RMSD bond angle0.988
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwarePHASER
Refinement softwarePHENIX (1.19.2_4158)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]47.3602.050
High resolution limit [Å]1.9901.990
Rpim0.0480.311
Number of reflections316321004
<I/σ(I)>12.72.8
Completeness [%]90.5
Redundancy6.1
CC(1/2)0.9950.797
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP2950.24 mM SPCC1393.13 protein in a buffer containing 5 mM CoCl2, 10 mM sodium pyrophosphate (pH 6.5), 18 mM Tris-HCl (pH 7.5), and 135 mM NaCl mixed with precipitant solution containing 0.1 M citric acid (pH 5.0) and 20% (w/v) PEG-6000

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