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1HV9

STRUCTURE OF E. COLI GLMU: ANALYSIS OF PYROPHOSPHORYLASE AND ACETYLTRANSFERASE ACTIVE SITES

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU
Temperature [K]293
Detector technologyIMAGE PLATE
Collection date1999-04-06
DetectorRIGAKU RAXIS IV
Wavelength(s)1.5418
Spacegroup nameH 3 2
Unit cell lengths104.500, 104.500, 648.200
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution30.250 - 2.100
R-factor0.211
Rwork0.211
R-free0.24800
Structure solution methodMIR
RMSD bond length0.008
RMSD bond angle1.300
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareSHARP
Refinement softwareX-PLOR (3.851)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.2502.180
High resolution limit [Å]2.1002.100
Rmerge0.136

*

0.233
Total number of observations495967

*

Number of reflections91622

*

<I/σ(I)>9.71.62
Completeness [%]98.0

*

82.2
Redundancy52.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.4293MES, ammonium sulfate, magnesium chloride, cobalt chloride, pH 6.4, VAPOR DIFFUSION, HANGING DROP, temperature 293.0K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein8.3 (mg/ml)
21dropUDP-GlcNAc14 (mM)
31drop28 (mM)
41drop19 (mM)
51reservoirammonium sulfate1.65 (M)
61reservoirMES50 (mM)
71reservoir2-10 (mM)

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