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1OH9

Acetylglutamate kinase from Escherichia coli complexed with MgADP, N-acetyl-L-glutamate and the transition-state mimic AlF4-

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE BW7B
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineBW7B
Temperature [K]100
Detector technologyCCD
Collection date2000-04-04
DetectorMARRESEARCH
Spacegroup nameC 2 2 21
Unit cell lengths59.457, 72.220, 107.214
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.000 - 1.910
R-factor0.1858
Rwork0.186
R-free0.22920
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1gs5
RMSD bond length0.005
RMSD bond angle1.250

*

Data reduction softwareMOSFLM
Data scaling softwareSCALA
Refinement softwareCNS (1.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0202.020
High resolution limit [Å]1.9101.910
Rmerge0.0370.144
Total number of observations89855

*

Number of reflections18025
<I/σ(I)>14.95.3
Completeness [%]99.095
Redundancy53.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

4.627-29% POLYETHYLENE GLYCOL MONOMETHYL ETHER 2K, SODIUM ACETATE 0.1M PH 4.6 AMMONIUM CITRATE 0.25-0.4 M
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirPEG200027-29 (%(w/v))
21reservoirsodium acetate0.1 (M)pH4.6
31reservoirammonium citrate0.25-0.4 (M)
41dropprotein10 (mg/ml)

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PDB entries from 2024-05-01

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