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1GK0

Structure-based prediction of modifications in glutarylamidase to allow single-step enzymatic production of 7-aminocephalosporanic acid from cephalosporin C

Experimental procedure
Experimental methodMAD
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE BM14
Synchrotron siteESRF
BeamlineBM14
Temperature [K]100
Detector technologyIMAGE PLATE
DetectorMAR scanner 345 mm plate
Wavelength(s)0.8854,0.9776,0.9779
Spacegroup nameC 1 2 1
Unit cell lengths228.366, 69.910, 113.550
Unit cell angles90.00, 97.57, 90.00
Refinement procedure
Resolution20.000

*

- 2.500
R-factor0.207
Rwork0.207
R-free0.22200
Structure solution methodMAD
RMSD bond length0.007
RMSD bond angle24.300

*

Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwareCNS
Refinement softwareCNS (1.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.600
High resolution limit [Å]2.5002.500
Rmerge0.0450.095
Number of reflections118686
Completeness [%]96.879.4
Redundancy2.051.63
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.5

*

18

*

CRYSTALS GROWN AT 18 C, HANGING DROP PRECIPITATION AGENT: 1.5-2.0 M POTASSIUM PHOSPHATE PH:7.0 -9.0, pH 8.00
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein20-30 (mg/ml)
21droppotassium phosphate0.5 (M)pH7.5
31dropdithiothreitol5 (mM)
41reservoirpotassium phosphate1.5-2.0pH7.0-9.0

219869

PDB entries from 2024-05-15

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