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6CD1

Crystal structure of Medicago truncatula serine hydroxymethyltransferase 3 (MtSHMT3), complexes with reaction intermediates

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-ID
Synchrotron siteAPS
Beamline19-ID
Temperature [K]100
Detector technologyPIXEL
Collection date2017-11-15
DetectorDECTRIS PILATUS 6M
Wavelength(s)0.9792
Spacegroup nameP 1 21 1
Unit cell lengths94.086, 103.653, 180.379
Unit cell angles90.00, 97.38, 90.00
Refinement procedure
Resolution46.650 - 1.910
R-factor0.191
Rwork0.191
R-free0.23600
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)6ccz
RMSD bond length0.012
RMSD bond angle1.529
Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwarePHASER
Refinement softwareREFMAC (5.8.0103)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.020
High resolution limit [Å]1.9101.910
Rmerge0.0630.730
Rmeas0.0710.830
Number of reflections26316541826
<I/σ(I)>13.31.9
Completeness [%]98.697.3
Redundancy4.74.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.529275 mM MES pH 6.5, 19% PEG3350 and 150 mM ammonium acetate. The mature crystals were soaked with 200 mM Ser for 2 h and cryoprotected by the addition of ethylene glycol to a final concentration of 20%

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