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5K9G

Crystal Structure of GTP Cyclohydrolase-IB with Tris

Replaces:  3D1T
Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL7-1
Synchrotron siteSSRL
BeamlineBL7-1
Temperature [K]100
Detector technologyCCD
Collection date2008-06-24
DetectorADSC QUANTUM 315
Wavelength(s)0.97670
Spacegroup nameC 2 2 21
Unit cell lengths92.707, 100.557, 114.017
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution68.160 - 1.900
R-factor0.17537
Rwork0.173
R-free0.22079
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3D1T
RMSD bond length0.020
RMSD bond angle1.992
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareREFMAC
Refinement softwareREFMAC (5.8.0107)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]68.1601.930
High resolution limit [Å]1.9001.900
Rmerge0.0470.355
Number of reflections41832
<I/σ(I)>36.172.05
Completeness [%]99.2
Redundancy4.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP8298(PEG 6000, 10-16%), LiCl (1-1.4 M), Tris (50 mM, pH 9.0) and Tris-Cl (50 mM, pH 7.0). Enzym sample prepared at 10 mg/mL in 50 mM Tris-HCl, 50 mM KCl, 1 mM DTT, pH 8.0

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