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3L17

Discovery of (thienopyrimidin-2-yl)aminopyrimidines as Potent, Selective, and Orally Available Pan-PI3-Kinase and Dual Pan-PI3-Kinase/mTOR Inhibitors for the Treatment of Cancer

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 5.0.2
Synchrotron siteALS
Beamline5.0.2
Detector technologyCCD
Collection date2006-06-09
DetectorADSC QUANTUM 315
Wavelength(s)1.0
Spacegroup nameC 1 2 1
Unit cell lengths144.095, 67.727, 107.455
Unit cell angles90.00, 96.07, 90.00
Refinement procedure
Resolution45.180 - 3.000
R-factor0.218
Rwork0.216
R-free0.27100
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1e8x
RMSD bond length0.012
RMSD bond angle1.316
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwarePHASER
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]50.00050.0003.110
High resolution limit [Å]3.0006.4603.000
Rmerge0.0740.0500.362
Number of reflections20541
<I/σ(I)>12.8
Completeness [%]97.899.883.1
Redundancy3.53.62.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP8.5289PEG 3350, 0.2M NH4SO4, 0.1M Tris-HCl 8.5, vapor diffusion, hanging drop, temperature 289K

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