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5AEG

A bacterial protein structure in glycoside hydrolase family 31.

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I04
Synchrotron siteDiamond
BeamlineI04
Temperature [K]293
Detector technologyPIXEL
Collection date2015-04-28
DetectorDECTRIS PILATUS 6M
Spacegroup nameP 1 21 1
Unit cell lengths78.665, 112.643, 111.881
Unit cell angles90.00, 109.52, 90.00
Refinement procedure
Resolution105.450 - 1.850
R-factor0.16189
Rwork0.160
R-free0.19337
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)5aed
RMSD bond length0.020
RMSD bond angle1.858
Phasing softwareMOLREP
Refinement softwareREFMAC (5.8.0095)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]49.6801.880
High resolution limit [Å]1.8501.850
Rmerge0.0500.620
Number of reflections154198
<I/σ(I)>13.52.1
Completeness [%]98.695.7
Redundancy43.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
16.529325 MG ML-1 YIHQ PROTEIN STOCK IS MIXED WITH EQUAL VOLUME OF PRECIPITANT COMPOSED OF 50-60% (V/V) 2-METHYL-2,4-PENTANEDIOL, 0.1-0.15 M CACL2, AND BIS-TRIS, (PH 6.5) AFTER 3-4 DAYS AT 20 DEGREE. THE LIGAND I5F WAS SOAKED INTO THE NATIVE CRYSTAL.

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