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1TOJ

Hydrocinnamic acid-bound structure of SRHEPT mutant of E. coli aspartate aminotransferase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 8.3.1
Synchrotron siteALS
Beamline8.3.1
Temperature [K]100
Detector technologyCCD
Collection date2003-12-23
DetectorADSC QUANTUM 210
Wavelength(s)1.12
Spacegroup nameC 2 2 21
Unit cell lengths83.412, 156.030, 77.865
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.000 - 1.900
R-factor0.18216
Rwork0.181
R-free0.20143
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ahx
RMSD bond length0.010
RMSD bond angle1.267
Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareREFMAC (5.2.0003)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0001.970
High resolution limit [Å]1.9001.900
Number of reflections40208
<I/σ(I)>253.7
Completeness [%]99.797.6
Redundancy3.53
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.5294potassium phosphate, PLP, EDTA, DTT, PEG 400, N-methylmorpholine, ammonium sulfate, hydrocinnamic acid, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 294K

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