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3O8T

Conformational plasticity of p38 MAP kinase DFG-motif mutants in response to inhibitor binding

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X4A
Synchrotron siteNSLS
BeamlineX4A
Temperature [K]93
Detector technologyCCD
DetectorADSC QUANTUM 4
Wavelength(s)0.98
Spacegroup nameP 21 21 21
Unit cell lengths68.489, 70.724, 75.682
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution37.840 - 2.000
R-factor0.22911
Rwork0.225
R-free0.28162
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1zyj
RMSD bond length0.012
RMSD bond angle1.454
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]37.8402.150
High resolution limit [Å]2.0002.000
Rmerge0.050
Number of reflections25513
<I/σ(I)>305
Completeness [%]90.893.4
Redundancy4.54.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP629510-20% PEG4000, 0.1M Cacodylic acid, 50 mM n-octyl-beta-D-glucoside, pH 6.0, VAPOR DIFFUSION, SITTING DROP, temperature 295K

250059

PDB entries from 2026-03-04

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