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1EHN

CRYSTAL STRUCTURE OF CHITINASE A MUTANT E315Q COMPLEXED WITH OCTA-N-ACETYLCHITOOCTAOSE (NAG)8.

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE BW7B
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineBW7B
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1999-04-04
DetectorMARRESEARCH
Spacegroup nameC 2 2 21
Unit cell lengths200.440, 131.617, 59.344
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution10.000 - 1.900
R-factor0.173

*

Rwork0.173
R-free0.21700
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1edq
RMSD bond length0.012
RMSD bond angle0.028
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]10.0001.970
High resolution limit [Å]1.9001.900
Rmerge0.0500.242

*

Number of reflections61168
<I/σ(I)>16.55.9
Completeness [%]99.0100
Redundancy4.14.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.218

*

0.75 M CITRATE-NA PH 7.2 AND 20% (V/V) METHANOL, VAPOR DIFFUSION, HANGING DROP, temperature 298K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein30 (mg/ml)
21reservoirsodium citrate0.75 (M)
31reservoirmethanol20 (%(v/v))

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