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5AEE

A bacterial protein structure in glycoside hydrolase family 31

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I02
Synchrotron siteDiamond
BeamlineI02
Temperature [K]193
Detector technologyPIXEL
Collection date2015-01-25
DetectorDECTRIS PILATUS 6M
Spacegroup nameP 1 21 1
Unit cell lengths77.960, 107.620, 103.300
Unit cell angles90.00, 107.85, 90.00
Refinement procedure
Resolution53.810 - 1.850
R-factor0.16446
Rwork0.163
R-free0.20090
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)5aed
RMSD bond length0.019
RMSD bond angle1.870
Phasing softwareREFMAC
Refinement softwareREFMAC (5.8.0131)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]53.8101.900
High resolution limit [Å]1.8501.850
Rmerge0.0500.880
Number of reflections121021
<I/σ(I)>13.51.2
Completeness [%]88.072.9
Redundancy3.42.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
16.529325 MG/ML-1 PROTEIN IN 50 MM NAPO4 , PH6.5, AND 250 MM NACL BUFFER 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 20 DEGREE

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