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1NQ6

Crystal Structure of the catalytic domain of xylanase A from Streptomyces halstedii JM8

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE BW7B
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineBW7B
Temperature [K]120
Detector technologyIMAGE PLATE
Collection date1996-07-22
DetectorMARRESEARCH
Wavelength(s)0.885
Spacegroup nameP 21 21 21
Unit cell lengths34.050, 79.600, 87.800
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution25.000

*

- 1.780
R-factor0.14745
Rwork0.145
R-free0.18000

*

Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1e0w
RMSD bond length0.009
RMSD bond angle1.090
Data reduction softwareDENZO
Data scaling softwareCCP4 ((SCALA))
Phasing softwareAMoRE
Refinement softwareREFMAC (5.1.24)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]25.000

*

1.880
High resolution limit [Å]1.780

*

1.780
Rmerge0.0440.084
Total number of observations78251

*

Number of reflections22905
<I/σ(I)>13.18.9
Completeness [%]97.185.8
Redundancy3.4

*

2.7

*

Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP5.5298PEG 4000, MAGNESIUM CHLORIDE, SODIUM ACETATE, pH 5.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein15 (mg/ml)
21reservoirPEG400010 (%)
31reservoir0.1 (M)
41reservoirsodium acetate0.1 (M)pH5.5

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