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1OZG

The crystal structure of Klebsiella pneumoniae acetolactate synthase with enzyme-bound cofactor and with an unusual intermediate

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 14-BM-D
Synchrotron siteAPS
Beamline14-BM-D
Temperature [K]100
Detector technologyCCD
Collection date2002-02-22
DetectorADSC QUANTUM 4
Wavelength(s)1.0
Spacegroup nameC 2 2 21
Unit cell lengths117.488, 160.561, 129.454
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution100.000 - 2.300
R-factor0.167
Rwork0.162
R-free0.21400
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1jsc
RMSD bond length0.005
RMSD bond angle1.230
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareCNS (1.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]100.0002.380
High resolution limit [Å]2.3002.300
Rmerge0.057

*

0.126

*

Total number of observations170273

*

Number of reflections484663030

*

<I/σ(I)>17.74.5
Completeness [%]88.249.3
Redundancy3.51.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7

*

17

*

PEG 8000, ethylene glycol, sodium HEPES , pH 7.6, VAPOR DIFFUSION, HANGING DROP, temperature 290K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropenzyme9 (mg/ml)
21droppotassium phosphate50 (mM)pH7.0
31dropThDP1 (mM)
41drop1 (mM)
51dropdithiothreitol1 (mM)
61reservoirsodium HEPES0.1 (M)pH7.5-7.7
71reservoirPEG80006-8 (%(w/v))
81reservoirethylene glycol6-9 (%(v/v))

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