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1QMG

Acetohydroxyacid isomeroreductase complexed with its reaction product dihydroxy-methylvalerate, manganese and ADP-ribose.

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE BM14
Synchrotron siteESRF
BeamlineBM14
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1996-06-15
DetectorMARRESEARCH
Spacegroup nameP 1 21 1
Unit cell lengths110.800, 61.200, 161.700
Unit cell angles90.00, 95.00, 90.00
Refinement procedure
Resolution10.000 - 1.600
R-factor0.193

*

Rwork0.196
R-free0.22500

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Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1yve
RMSD bond length0.008
RMSD bond angle1.700

*

Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareX-PLOR (3.851)
Refinement softwareX-PLOR (3.851)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]26.0001.640
High resolution limit [Å]1.6001.600
Rmerge0.054

*

0.096

*

Number of reflections299230
<I/σ(I)>18.814.6
Completeness [%]96.696.6
Redundancy2.92.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

7.5

*

20

*

Dumas, R., (1994) J. Mol. Biol., 242, 578.

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein0.020mg
21dropHEPES-KOH20 (mM)
31reservoirammonium sulfate2 (M)
41reservoirTris-HCl0.1 (M)

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PDB entries from 2024-07-10

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