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1M1B

Crystal Structure of Phosphoenolpyruvate Mutase Complexed with Sulfopyruvate

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsSIEMENS
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date2001-05-25
DetectorMARRESEARCH
Wavelength(s)1.5418
Spacegroup nameC 2 2 21
Unit cell lengths90.024, 130.441, 90.475
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution26.500 - 2.250
R-factor0.185
Rwork0.179
R-free0.26800
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1pym
RMSD bond length0.009
RMSD bond angle1.500

*

Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareCNS (1.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]26.5002.290
High resolution limit [Å]2.2502.250
Rmerge0.0640.244
Number of reflections21045
<I/σ(I)>13.83.7
Completeness [%]83.364.9
Redundancy5.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.5298PEG 4000, glycerol, magnesium chloride, Hepes, sulfopyruvate, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirPEG700018 (%(w/v))
21reservoirglycerol15 (%)
31reservoir5 (mM)
41reservoirHEPES100 (mM)pH7.0-8.0
51dropprotein9 (mg/ml)
61dropS-pyr5 (mM)

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