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8QSV

Bi-allelic variants of SPOUT1, a novel RNA methyltransferase, cause chromosome missegregation and a rare neurodevelopmental disease

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I03
Synchrotron siteDiamond
BeamlineI03
Temperature [K]100
Detector technologyPIXEL
Collection date2014-07-05
DetectorDECTRIS EIGER2 XE 16M
Wavelength(s)0.97000
Spacegroup nameC 2 2 21
Unit cell lengths75.070, 80.830, 135.690
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution55.010 - 2.620
R-factor0.20662
Rwork0.203
R-free0.28020
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.008
RMSD bond angle1.583
Data reduction softwareXDS
Data scaling softwarexia2
Phasing softwarePHENIX
Refinement softwareREFMAC (5.8.0411)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]55.0102.880
High resolution limit [Å]2.6202.620
Rmerge0.0860.663
Rmeas0.0930.720
Rpim0.0360.276
Number of reflections126263066
<I/σ(I)>16.113.81
Completeness [%]99.198.02
Redundancy6.56.6
CC(1/2)0.9980.947
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP6.52910.06 M MgCl2, CaCl2 or 0.09 M NaF, NaBr, NaI with 0.1 M Imidazole, MES (acid) pH 6.5 and 30 % Ethylene glycol, PEG 8K

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