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3L8Z

H-Ras wildtype new crystal form

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSLS BEAMLINE X10SA
Synchrotron siteSLS
BeamlineX10SA
Temperature [K]100
Detector technologyCCD
Collection date2007-10-28
DetectorMARMOSAIC 225 mm CCD
Wavelength(s)1.28350
Spacegroup nameH 3 2
Unit cell lengths88.082, 88.082, 133.391
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution19.730 - 1.440
R-factor0.193
Rwork0.191
R-free0.22000
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)5p21
RMSD bond length0.009
RMSD bond angle1.911
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwareMOLREP
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.480
High resolution limit [Å]1.4401.440
Rmerge0.0360.335
Number of reflections34928
<I/σ(I)>24.93.59
Completeness [%]96.482.1
Redundancy10.694.67
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.528517% PEG6000, 200mM CaCl2, 30mM TRIS/HCL, 5mM MgCl2, 2mM DTE, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 285K

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