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3KPA

Ubiquitin fold modifier conjugating enzyme from Leishmania major (probable)

Experimental procedure
Experimental methodMAD
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 8.2.2
Synchrotron siteALS
Beamline8.2.2
Temperature [K]100
Detector technologyCCD
Collection date2003-08-12
DetectorADSC QUANTUM 315
Wavelength(s)0.9784
Spacegroup nameP 1 21 1
Unit cell lengths57.274, 34.133, 126.774
Unit cell angles90.00, 99.32, 90.00
Refinement procedure
Resolution50.000 - 2.200
R-factor0.217
Rwork0.214
R-free0.27300
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2in1
RMSD bond length0.010
RMSD bond angle1.220
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareBALBES
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.370
High resolution limit [Å]2.2002.200
Rmerge0.1020.394
Number of reflections23133
<I/σ(I)>11.42.2
Completeness [%]91.470.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION6293protein buffer 25 mM HEPES pH 7.5, 120 mM NaCl; crystallization buffer 100 mM Na Cacodylate, 300 mM Ammonium Sulfate,, 30% PEG 4000, vapor diffusion, temperature 293K

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