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1RTU

USTILAGO SPHAEROGENA RIBONUCLEASE U2

Experimental procedure
Source typeSYNCHROTRON
Source detailsPHOTON FACTORY
Synchrotron sitePhoton Factory
Temperature [K]284
Detector technologyIMAGE PLATE
Collection date1990-05-22
DetectorFUJI
Spacegroup nameP 21 21 21
Unit cell lengths49.320, 61.270, 34.950
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution8.000 - 1.800
R-free0.17800

*

Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)RNASE T1 (PDB ENTRY 1RNT)
RMSD bond length0.014
RMSD bond angle0.028
Data reduction softwareTOMOKO
Data scaling softwareA (PROGRAM BY TOMOKO)
Phasing softwareX-PLOR
Refinement softwarePROLSQ
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]12.0001.870
High resolution limit [Å]1.8001.800
Rmerge0.044

*

0.077
Number of reflections9903
Completeness [%]96.186.4
Redundancy43
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

4.520

*

CRYSTALS WERE PREPARED BY HANGING-DROP VAPOUR-DIFFUSION METHOD AT 293 KELVIN FROM A 20 MG/ML PROTEIN SOLUTION CONTAINING 15 MG/ML 2'-DEOXY 2'-FLUORO ADENYLYL-3',5'-CYTIDINE, 0.4M AMMONIUM SULFATE, EQUILIBRATED AGAINST A RESERVOIR OF 0.9M AMMONIUM SULFATE CONTAINING 0.1M ACETATE BUFFER (PH 4.5)., vapor diffusion - hanging drop
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein20 (mg/ml)
21drop2'-deoxy-2'-fluro ApC1.5 (mg/ml)
31dropammonium sulfate0.9 (M)
41reservoirammonium sulfate0.9 (M)
51reservoiracetate0.1 (M)

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