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1QAG

Actin binding region of the dystrophin homologue utrophin

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE BM14
Synchrotron siteESRF
BeamlineBM14
Temperature [K]100
Detector technologyCCD
Collection date1998-01-21
DetectorPRINCETON 2K
Wavelength(s)0.9000, 0.9795, 0.9809
Spacegroup nameC 1 2 1
Unit cell lengths150.145, 55.160, 80.420
Unit cell angles90.00, 106.06, 90.00
Refinement procedure
Resolution99.000 - 3.000
R-factor0.198

*

Rwork0.198
R-free0.25800
Structure solution methodMAD
RMSD bond length0.007
RMSD bond angle1.200
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareSHELXS
Refinement softwareX-PLOR (3.851)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]24.000

*

3.160
High resolution limit [Å]3.0003.000
Rmerge0.0570.146
Number of reflections12342
<I/σ(I)>85.1
Completeness [%]96.797.2
Redundancy2.72.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

4.7

*

20

*

0.1M Sodium Acetate pH 4.7, 2.0 M unbuffered sodium formate., pH 5.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111Sodium Acetate
211sodium formate
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein50 (mg/ml)
21reservoir2.0 (M)
31reservoirsodium acetate0.1 (M)

222036

PDB entries from 2024-07-03

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