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7R8X

Crystal Structure of the LNK SH2 Domain in Complex with an EPOR pY454 Phosphopeptide

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAUSTRALIAN SYNCHROTRON BEAMLINE MX2
Synchrotron siteAustralian Synchrotron
BeamlineMX2
Temperature [K]100
Detector technologyPIXEL
Collection date2018-06-21
DetectorDECTRIS EIGER X 16M
Wavelength(s)0.953740
Spacegroup nameP 61
Unit cell lengths86.157, 86.157, 38.052
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution33.900 - 2.300
R-factor0.1998
Rwork0.197
R-free0.23050
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2hdv
Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwarePHENIX
Refinement softwarePHENIX (1.19.2_4158)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]33.9002.383
High resolution limit [Å]2.3002.301
Rmerge0.0440.492
Rmeas0.0470.539
Rpim0.015
Number of reflections7318724
<I/σ(I)>312.81
Completeness [%]99.899.45
Redundancy9.6
CC(1/2)1.0000.904
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP9.5277.1520% PEG8000, 0.05 M magnesium acetate, 0.1 M Tris, ph 8.5

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