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6UXI

Structure of serine hydroxymethyltransferase 8 from Glycine max cultivar Essex complexed with PLP-Glycine

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 5.0.1
Synchrotron siteALS
Beamline5.0.1
Temperature [K]100
Detector technologyPIXEL
Collection date2018-08-11
DetectorDECTRIS PILATUS 6M
Wavelength(s)1.00
Spacegroup nameP 2 21 21
Unit cell lengths56.567, 124.547, 129.125
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution47.839 - 2.100
R-factor0.1862
Rwork0.184
R-free0.22340
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)6uxh
Data reduction softwareXDS
Data scaling softwareAimless (0.7.3)
Phasing softwarePHASER
Refinement softwarePHENIX (1.14_3260)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]47.8402.160
High resolution limit [Å]2.1002.100
Rmerge0.1441.828
Rmeas0.1571.986
Rpim0.0610.767
Total number of observations35315628628
Number of reflections541014371
<I/σ(I)>10.51.1
Completeness [%]99.9100
Redundancy6.56.5
CC(1/2)0.9970.311
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP2930.19 M trimethylamine N-oxide, 0.1 M Tris (pH 8.5), 21% (w/v) PEG MME 2000, 20 mM glycine

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