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3OOO

The structure of a proline dipeptidase from Streptococcus agalactiae 2603V

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-ID
Synchrotron siteAPS
Beamline19-ID
Temperature [K]100
Detector technologyCCD
Collection date2010-06-27
DetectorADSC QUANTUM 315r
Wavelength(s)0.9792
Spacegroup nameP 21 21 21
Unit cell lengths43.744, 58.325, 101.995
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution50.000 - 1.570
R-factor0.18788
Rwork0.186
R-free0.21473
Structure solution methodSAD
RMSD bond length0.007
RMSD bond angle1.039
Data reduction softwareHKL-3000
Data scaling softwareHKL-3000
Phasing softwareSHELXD
Refinement softwareREFMAC (5.5.0109)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.600
High resolution limit [Å]1.5701.570
Rmerge0.0500.142
Number of reflections37273
<I/σ(I)>40.6
Completeness [%]99.390.8
Redundancy4.73.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.52970.2M sodium chloride, 0.1M HEPES pH7.5, 20%v/v 1,4-butanediol, VAPOR DIFFUSION, SITTING DROP, temperature 297K

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