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2GHP

Crystal structure of the N-terminal 3 RNA binding domains of the yeast splicing factor Prp24

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 22-ID
Synchrotron siteAPS
Beamline22-ID
Temperature [K]100
Detector technologyCCD
Collection date2005-10-11
DetectorMARMOSAIC 300 mm CCD
Wavelength(s)0.97911
Spacegroup nameP 21 21 21
Unit cell lengths114.608, 125.848, 196.542
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution49.503 - 2.700
Rwork0.213
R-free0.26420
Structure solution methodSAD
RMSD bond length0.012
RMSD bond angle1.380
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareSHARP
Refinement softwareREFMAC (5.2.0005)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]49.50349.5002.800
High resolution limit [Å]2.7005.8202.700
Rmerge0.1220.0840.489
Number of reflections74236
<I/σ(I)>7.4162.39
Completeness [%]94.299.774.3
Redundancy77.25.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP277PROTEIN SOLUTION (10 MG/ML PROTEIN, 0.050 M SODIUM CHLORIDE, 0.0003 M TCEP, 0.005 TRIS PH 8.0) MIXED IN A 1:1 RATIO WITH THE WELL SOLUTION (14% MEPEG 5000, 0.20 M TETRAMETHYL AMMONIUM CHLORIDE, 0.10 M SODIUM SUCCINATE PH 4.0) Crystals cryo-protected with the well solution supplemented with 30% ethylene glycol., VAPOR DIFFUSION, HANGING DROP, temperature 277K

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