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1HD2

Human peroxiredoxin 5

Experimental procedure
Experimental methodMAD
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE X31
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineX31
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date2000-09-15
DetectorMAR scanner 345 mm plate
Wavelength(s)1.1,0.9175,0.9169,0.855
Spacegroup nameP 41 21 2
Unit cell lengths66.607, 66.607, 123.327
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution16.000 - 1.500
R-factor0.1325
R-free0.16450
Structure solution methodMAD
RMSD bond length0.015
RMSD bond angle0.026
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareMLPHARE
Refinement softwareSHELXL-97
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]16.0001.720
High resolution limit [Å]1.5001.500
Rmerge0.0510.246
Total number of observations384543

*

Number of reflections45181
<I/σ(I)>247
Completeness [%]100.0100
Redundancy8.58
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

5.318

*

PROTEIN WAS CRYSTALLIZED FROM 1.6 M AMMONIUM SULFATE, 0.1 M SODIUM CITRATE BUFFER PH 5.3, 0.2 M POTASSIUM SODIUM TARTRATE, 1 MM DTT, 0.02 % (W/V) SODIUM AZIDE
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein10 (mg/ml)
21reservoirammonium sulfate1.6 (M)
31reservoirsodium citrate0.1 (M)
41reservoirpotassium/sodium tartrate0.2 (M)
51reservoir1,4-dithio-DL-threitol0.001 (M)
61reservoirsodium azide0.02 (%(w/v))

219869

PDB entries from 2024-05-15

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