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3DCY

Crystal Structure a TP53-induced glycolysis and apoptosis regulator protein from Homo sapiens.

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 23-ID-D
Synchrotron siteAPS
Beamline23-ID-D
Temperature [K]100
Detector technologyCCD
Collection date2008-04-04
DetectorMARMOSAIC 300 mm CCD
Wavelength(s)0.97942
Spacegroup nameP 21 21 21
Unit cell lengths40.983, 76.408, 79.536
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution50.000 - 1.748
R-factor0.182
Rwork0.180
R-free0.22900
Structure solution methodSAD
RMSD bond length0.015
RMSD bond angle1.479
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareSHARP
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]50.00050.0001.810
High resolution limit [Å]1.7483.7701.750
Rmerge0.1090.0680.540
Number of reflections25927
<I/σ(I)>16.2232.369
Completeness [%]99.899.998.4
Redundancy13.913.89.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6297PROTEIN SOLUTION (10 MG/ML SEMET PROTEIN, 0.050 M NACL, 0.0003 M TCEP, 0.005 M MES PH 6.0) MIXED IN A 1:1 RATIO WITH WELL SOLUTION (20% PEG 3350, 0.10 M MES PH 6.0) CRYOPROTECTED WITH 20% ETHYLENE GLYCOL, VAPOR DIFFUSION, HANGING DROP, TEMPERATURE 297K

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