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4PGM

SACCHAROMYCES CEREVISIAE PHOSPHOGLYCERATE MUTASE

Experimental procedure
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE X31
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineX31
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1996-11
DetectorMARRESEARCH
Spacegroup nameP 1 21 1
Unit cell lengths81.467, 84.555, 88.884
Unit cell angles90.00, 111.72, 90.00
Refinement procedure
Resolution25.000 - 2.300
R-factor0.192
Rwork0.192
R-free0.28600
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3pgm
RMSD bond length0.011
RMSD bond angle23.524

*

Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareX-PLOR (3.843)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]25.0002.380
High resolution limit [Å]2.3002.300
Rmerge0.082

*

0.253
Number of reflections49635
<I/σ(I)>4.852.41
Completeness [%]88.789.9
Redundancy6.272.15
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, sitting drop

*

8.65PROTEIN WAS CRYSTALLISED FROM 22-24% PEG 4000 60MM TRIS-HCL, PH 8.65, 120MM LI2SO4, AND 1MM INOSITOL HEXAKISPHOSPHATE
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein10 (mg/ml)
21dropinositol hexakisphosphate1 (mM)
31reservoirTris-HCl60 (mM)pH8.65
41reservoirlithium sulfate120 (mM)
51reservoirPEG400022-24 (%)

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