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1R3N

Crystal structure of beta-alanine synthase from Saccharomyces kluyveri

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-1
Synchrotron siteESRF
BeamlineID14-1
Temperature [K]100
Detector technologyCCD
Collection date2001-12-10
DetectorADSC QUANTUM 4
Wavelength(s)0.933
Spacegroup nameP 1 21 1
Unit cell lengths117.230, 77.120, 225.520
Unit cell angles90.00, 95.05, 90.00
Refinement procedure
Resolution30.000

*

- 2.700
R-factor0.21118
Rwork0.208
R-free0.26600

*

Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)model of seleno-methionine substituted beta-alanine synthase from the same source
RMSD bond length0.009
RMSD bond angle1.200

*

Data reduction softwareMOSFLM
Data scaling softwareCCP4 ((SCALA))
Phasing softwareEPMR
Refinement softwareREFMAC (5.1.24)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]25.0002.850
High resolution limit [Å]2.7002.700
Rmerge0.0830.261
Number of reflections106190
<I/σ(I)>14.83.7
Completeness [%]95.982.2
Redundancy3.52.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.5

*

20

*

trisodium citrate, dioxane, pH 6.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein4.0-4.5 (mg/ml)
21dropTris50 (mM)pH7.5
31dropdithiothreitol1 (mM)
41drop100 (mM)
51reservoirtrisodium citrate0.88 (M)
61reservoirsodium citrate0.1 (M)pH6.0
71reservoirdioxane5 (%(v/v))

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