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1HL5

The Structure of Holo Type Human Cu, Zn Superoxide Dismutase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSRS BEAMLINE PX14.2
Synchrotron siteSRS
BeamlinePX14.2
Temperature [K]100
Detector technologyCCD
Collection date2002-01-15
DetectorADSC CCD
Spacegroup nameP 1 21 1
Unit cell lengths76.871, 172.380, 112.450
Unit cell angles90.00, 93.45, 90.00
Refinement procedure
Resolution50.000 - 1.780

*

R-factor0.187
Rwork0.185
R-free0.22200
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1sos
RMSD bond length0.014
RMSD bond angle1.604
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareMOLREP
Refinement softwareREFMAC (5.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.860
High resolution limit [Å]1.780

*

1.780

*

Rmerge0.0520.350
Total number of observations904897

*

Number of reflections265996
<I/σ(I)>202.7
Completeness [%]98.696.3
Redundancy3.43
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

80.2 M CA ACETATE, 15% PEG 3350, 0.1 M TRIS PH 8.0
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein6 (mg/ml)
21dropPEG33507.5 (%(w/v))
31dropcalcium acetate100 (mM)
41dropTris50 (mM)pH8.0
51reservoirPEG335015 (%)
61reservoircalcium acetate200 (mM)
71reservoirTris-HCl100 (mM)pH8.0

222036

PDB entries from 2024-07-03

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