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2ORM

Crystal Structure of the 4-Oxalocrotonate Tautomerase Homologue DmpI from Helicobacter pylori.

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RU200
Temperature [K]108
Detector technologyIMAGE PLATE
Collection date2000-08-10
DetectorRIGAKU RAXIS IV
Spacegroup nameP 1 21 1
Unit cell lengths41.830, 50.770, 89.310
Unit cell angles90.00, 99.13, 90.00
Refinement procedure
Resolution24.500 - 2.100
R-factor0.217
Rwork0.217
R-free0.24900
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1bjp
RMSD bond length0.007
RMSD bond angle1.100
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]24.5002.180
High resolution limit [Å]2.1002.100
Number of reflections20368
<I/σ(I)>13.54
Completeness [%]90.090
Redundancy5.94
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
17.52772 uL of protein (20 mg/mL) in 20mM phosphate buffer (pH 7.4) were mixed with 2 uL of 0.2M CaCl2, 0.1M Hepes (pH 7.5), and 28% PEG 400. This combined volume was equilibrated at 4 degrees Celcius against 50 uL of 0.2M CaCl2, 0.1M Hepes (pH 7.5), and 28% PEG 400 , VAPOR DIFFUSION, SITTING DROP, temperature 277K, pH 7.50

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