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7RUM

Endolysin from Escherichia coli O157:H7 phage FTEbC1, LysT84

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAUSTRALIAN SYNCHROTRON BEAMLINE MX2
Synchrotron siteAustralian Synchrotron
BeamlineMX2
Temperature [K]110
Detector technologyPIXEL
Collection date2019-03-19
DetectorDECTRIS EIGER X 16M
Wavelength(s)0.9537
Spacegroup nameP 65 2 2
Unit cell lengths106.928, 106.928, 369.259
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution49.040 - 2.990
R-factor0.2346
Rwork0.233
R-free0.27220
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)5nm7
RMSD bond length0.002
RMSD bond angle0.519
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwarePHASER
Refinement softwarePHENIX (1.19-40)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]49.04049.0403.170
High resolution limit [Å]2.9908.9702.990
Rmerge0.5210.0923.403
Rmeas0.5350.0953.509
Rpim0.1240.0240.841
Total number of observations4874181857370198
Number of reflections2640111644115
<I/σ(I)>6.619.71.1
Completeness [%]99.999.599.5
Redundancy18.51617.1
CC(1/2)0.9740.9710.554
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP293.15Morpheus I condition F3: 0.12 M monosaccharides [0.2 M D-glucose; 0.2 M D-mannose; 0.2 M D-galactose; 0.2 M L-fucose; 0.2 M D-xylose; 0.2 M N-acetyl-D-glucosamine] 0.1 M buffer System 1 [1.0 M imidazole; MES monohydrate (acid) pH 6.5], 30% v/v Precipitant Mix 3 [40% v/v glycerol; 20% w/v PEG 4000

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