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7KSJ

Thiophenyl-Pyrazolourea Derivatives as Potent, Brian Penetrant, Orally Bioavailable, and Isoform-Selective JNK3 Inhibitors

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 21-ID-F
Synchrotron siteAPS
Beamline21-ID-F
Temperature [K]100
Detector technologyCCD
Collection date2017-09-21
DetectorRAYONIX MX300HE
Wavelength(s)0.97872
Spacegroup nameP 21 21 21
Unit cell lengths51.451, 71.237, 107.804
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution41.710 - 2.060
R-factor0.2331
Rwork0.230
R-free0.29170
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1jnk
RMSD bond length0.008
RMSD bond angle0.940
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwarePHASER
Refinement softwareBUSTER (2.10.3 (19-MAR-2020))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]53.8732.095
High resolution limit [Å]2.0602.060
Number of reflections236261199
<I/σ(I)>12.72.6
Completeness [%]93.7
Redundancy4.2
CC(1/2)0.9990.940
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP277.150.2 M ammonium tartrate pH 7.0, 20 % PEG 3350

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