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3H11

Zymogen caspase-8:c-FLIPL protease domain complex

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X29A
Synchrotron siteNSLS
BeamlineX29A
Temperature [K]100
Detector technologyCCD
Collection date2008-10-31
DetectorADSC QUANTUM 315
Wavelength(s)1.10
Spacegroup nameP 21 21 21
Unit cell lengths52.990, 76.680, 114.190
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution45.800 - 1.900
R-factor0.212
Rwork0.212
R-free0.25000
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.010
RMSD bond angle1.500
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwarePHASER
Refinement softwareCNS (1.2)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]100.0001.970
High resolution limit [Å]1.9001.900
Number of reflections37398
<I/σ(I)>13.52.7
Completeness [%]99.699.7
Redundancy4.74.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP10.52930.9 M sodium dihydrogen phosphate, 0.8 M dipotassium hydrogen phosphate, 0.1 M N-cyclohexyl-3-aminopropanesulfonic acid (CAPS), 0.2 M lithium sulfate, pH 10.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K

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