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2JC4

3'-5' exonuclease (NExo) from Neisseria Meningitidis

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSRS BEAMLINE PX14.1
Synchrotron siteSRS
BeamlinePX14.1
Temperature [K]100
Detector technologyCCD
DetectorADSC CCD
Spacegroup nameP 21 21 21
Unit cell lengths46.193, 58.618, 88.635
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution19.960 - 1.900
Rwork0.152
R-free0.20200
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1bix
RMSD bond length0.016
RMSD bond angle1.501
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareMOLREP
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.970
High resolution limit [Å]1.9001.900
Rmerge0.0900.320
Number of reflections19164
<I/σ(I)>24.55.1
Completeness [%]97.691.4
Redundancy6.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
16.5PROTEIN CONCENTRATION 8.7MG/ML BUFFER: 10 MM TRIS, PH 7.0, 100 MM NACL . WELL SOLUTION: 100 MM NA CACODYLATE PH 6 200 MM NA ACETATE, 15 % PEG 8000. THE CRYSTALLISATION PLATES USED WERE CORNING ROUND BOTTOM 96 WELL PLATES. THE CRYSTALLISATION DROPS CONSISTED OF 1UL PROTEIN AND 1UL WELL SOLUTION.

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