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4G1K

Crystal structure of triosephosphate isomerase from Burkholderia thailandensis

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 5.0.3
Synchrotron siteALS
Beamline5.0.3
Temperature [K]100
Detector technologyCCD
Collection date2012-06-29
DetectorADSC QUANTUM 315r
Wavelength(s)0.9765
Spacegroup nameP 21 21 21
Unit cell lengths79.510, 94.750, 170.610
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution50.000 - 2.350
R-factor0.1712
Rwork0.170
R-free0.20230
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.014
RMSD bond angle1.476
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwarePHASER (2.3.0)
Refinement softwareREFMAC (5.6.0117)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]50.0002.410
High resolution limit [Å]2.35010.5102.350
Rmerge0.1210.0240.506
Number of reflections544616913989
<I/σ(I)>15.351.373.83
Completeness [%]99.998.699.8
Redundancy6.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP4.6289ButhA.00317.a.A1 PS01252 at 18 mg/mL against JCSG+ condition B7, 0.1 M Na acetate pH 4.6, 8% PEG 4000 with 20% ethylene glycol as cryo-protectant, crystal tracking ID 227610b7, unique puck ID kyb3-5, VAPOR DIFFUSION, SITTING DROP, temperature 289K

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