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6UHL

Crystal Structure of C148 mGFP-scDNA-1

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 21-ID-F
Synchrotron siteAPS
Beamline21-ID-F
Temperature [K]100
Detector technologyCCD
Collection date2018-07-03
DetectorRAYONIX MX-300
Wavelength(s)0.97872
Spacegroup nameP 1 21 1
Unit cell lengths64.870, 52.290, 86.800
Unit cell angles90.00, 94.13, 90.00
Refinement procedure
Resolution43.290 - 1.910
R-factor0.2304
Rwork0.228
R-free0.27300
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4eul
RMSD bond length0.009
RMSD bond angle1.776
Data reduction softwarexia2
Data scaling softwareAimless
Phasing softwarePHENIX
Refinement softwareREFMAC (5.8.0257)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]43.29043.2901.960
High resolution limit [Å]1.9108.5401.910
Rmerge0.1220.0511.313
Rmeas0.1280.0541.444
Rpim0.0400.0170.579
Total number of observations435564
Number of reflections439455472202
<I/σ(I)>12.129.41.3
Completeness [%]96.998.667.2
Redundancy9.99.25.8
CC(1/2)0.9980.9980.492
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP2951 microliter C148 mGFP-scDNA-1 (5 mg/mL (protein concentration) in 10 mM Tris Buffer pH 7.4, 137 mM NaCl) + 1 microliter crystallization condition (0.1 M SPG Buffer pH 8, 25% (w/v) PEG 1500) in a sitting drop with a 70 microliter reservoir (0.1 M SPG Buffer pH 8, 25% (w/v) PEG 1500)

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PDB entries from 2024-05-15

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