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9V17

Crystal structure of E. coli glycogen phosphorylase N185A/R267E mutant

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSPRING-8 BEAMLINE BL44XU
Synchrotron siteSPring-8
BeamlineBL44XU
Temperature [K]100
Detector technologyPIXEL
Collection date2025-04-23
DetectorDECTRIS EIGER X 16M
Wavelength(s)0.9
Spacegroup nameP 41 21 2
Unit cell lengths187.297, 187.297, 449.824
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution49.600 - 3.700
R-factor0.1975
Rwork0.196
R-free0.22940
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.003
RMSD bond angle0.642
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwareMOLREP
Refinement softwarePHENIX (1.19.2_4158)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]49.6003.770
High resolution limit [Å]3.7003.700
Rmerge0.2482.950
Rmeas0.2623.130
Rpim0.0820.995
Number of reflections848104444
<I/σ(I)>91.1
Completeness [%]98.999.3
Redundancy9.29
CC(1/2)0.9970.782
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP2932% v/v 1,4-dioxane, 0.1M Tris pH 8.0, 15% w/v polyethylene glycol 3350

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