Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

3L16

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 lengths142.635, 67.391, 106.674
Unit cell angles90.00, 96.11, 90.00
Refinement procedure
Resolution20.000 - 2.900
R-factor0.241
Rwork0.238
R-free0.29500
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1e8x
RMSD bond length0.010
RMSD bond angle1.278
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwarePHASER
Refinement softwareREFMAC
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]40.00040.0002.800
High resolution limit [Å]2.7005.8102.700
Rmerge0.0440.0250.440
Number of reflections27593
<I/σ(I)>20.7
Completeness [%]98.194.298.5
Redundancy3.23.13.2
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

222415

PDB entries from 2024-07-10

PDB statisticsPDBj update infoContact PDBjnumon