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6UXH

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

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 4.2.2
Synchrotron siteALS
Beamline4.2.2
Temperature [K]100
Detector technologyCMOS
Collection date2018-03-15
DetectorRDI CMOS_8M
Wavelength(s)1.00
Spacegroup nameP 2 21 21
Unit cell lengths55.640, 126.820, 128.570
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution42.070 - 1.858
R-factor0.2005
Rwork0.199
R-free0.23120
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1cj0
Data reduction softwareXDS
Data scaling softwareAimless (0.6.2)
Phasing softwarePHASER
Refinement softwarePHENIX (1.14-3260)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]47.3701.890
High resolution limit [Å]1.8501.850
Rmerge0.1012.124
Rmeas0.1062.306
Rpim0.0300.888
Total number of observations95792529349
Number of reflections781064367
<I/σ(I)>19.20.8
Completeness [%]99.699.7
Redundancy12.36.7
CC(1/2)0.9990.636
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP2930.175 M trimethylamine N-oxide, 0.1 M Tris (pH 8.5), 19.5% (w/v) PEG MME 2000

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