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2JBW

Crystal Structure of the 2,6-dihydroxy-pseudo-oxynicotine Hydrolase.

Experimental procedure
Experimental methodMAD
Source typeSYNCHROTRON
Source detailsBESSY BEAMLINE 14.1
Synchrotron siteBESSY
Beamline14.1
Temperature [K]100
Detector technologyCCD
DetectorMARRESEARCH
Spacegroup nameP 1 21 1
Unit cell lengths90.570, 57.020, 152.697
Unit cell angles90.00, 103.35, 90.00
Refinement procedure
Resolution30.000 - 2.100
R-factor0.183
Rwork0.181
R-free0.23800
Structure solution methodMAD
RMSD bond length0.022
RMSD bond angle1.527
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwareSHELXD
Refinement softwareREFMAC (5.2.0005)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]35.0002.160
High resolution limit [Å]2.1002.090
Rmerge0.0500.250
Number of reflections172409
<I/σ(I)>11.53.3
Completeness [%]99.498
Redundancy1.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP8.8PROTEINSOLUTION: 50 MM TRIS-HCL PH 7.4, 200 MM NACL, 0.5 M TCEP RESERVOIR: 35% PEG 10000, O.1 M TRIS-HCL PH 8.8 HANGING DROP, MIXED 1:1, MICROSEEDING

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PDB entries from 2024-07-10

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