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28ZO

Crystal structure of human DHX8 in complex with compound 24 and ADP

This is a non-PDB format compatible entry.
Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I04
Synchrotron siteDiamond
BeamlineI04
Temperature [K]100
Detector technologyPIXEL
Collection date2018-04-21
DetectorDECTRIS EIGER2 XE 16M
Wavelength(s)0.9795
Spacegroup nameP 1 21 1
Unit cell lengths66.881, 167.127, 137.101
Unit cell angles90.00, 92.47, 90.00
Refinement procedure
Resolution136.970 - 2.970
R-factor0.2158
Rwork0.214
R-free0.25270
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.007
RMSD bond angle0.860
Data reduction softwareDIALS
Data scaling softwareAimless (0.7.1)
Phasing softwarePHASER
Refinement softwareBUSTER (2.10.4 (26-JUL-2023))
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]167.130167.1303.050
High resolution limit [Å]2.97013.2802.970
Rmerge0.2120.0670.904
Rmeas0.2370.0781.005
Rpim0.1040.0390.435
Total number of observations315672344824230
Number of reflections620647264643
<I/σ(I)>5.416.21.4
Completeness [%]100.099.9100
Redundancy5.14.75.2
CC(1/2)0.9780.9820.311
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP5.52910.5 microliter of DHX8del547 at 3 mg/mL with 1 mM ADP and 1 mM MgCl2, plus 1.5 microliter of a crystallisation solution consisting of 15% (v/v) MPD, 100 mM Sodium Acetate pH 5.5 and 6% (v/v) DMSO, against 250 microliter of crystallisation solution

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