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1X27

Crystal Structure of Lck SH2-SH3 with SH2 binding site of p130Cas

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-1
Synchrotron siteESRF
BeamlineID14-1
Temperature [K]100
Detector technologyCCD
Collection date2004-02-28
DetectorMARRESEARCH
Wavelength(s)0.93400
Spacegroup nameP 21 21 21
Unit cell lengths77.415, 107.289, 166.389
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.000 - 2.700
R-factor0.247
Rwork0.247
R-free0.31700
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1lck
RMSD bond length0.008
RMSD bond angle1.300
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.850
High resolution limit [Å]2.7002.700
Rmerge0.073
Number of reflections37482
<I/σ(I)>7.21.5
Completeness [%]96.696
Redundancy3.53.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP9295N-tris[hydroxymethyl]methyl-3-aminopropane-sulfonic acid, di_potasium hydrogen phosphate, pH 9.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K

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