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1OIR

Imidazopyridines: a potent and selective class of Cyclin-dependent Kinase inhibitors identified through Structure-based hybridisation

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSRS BEAMLINE PX9.6
Synchrotron siteSRS
BeamlinePX9.6
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1998-07-15
DetectorMARRESEARCH
Spacegroup nameP 21 21 21
Unit cell lengths53.529, 72.239, 72.137
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution43.030 - 1.910
R-factor0.205
Rwork0.204
R-free0.23700

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Structure solution methodMOLECULAR REPLACEMENT
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareAMoRE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]43.0302.010
High resolution limit [Å]1.9101.900
Rmerge0.052

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0.137
Total number of observations95201

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Number of reflections20394
<I/σ(I)>21.710.3
Completeness [%]84.873.3
Redundancy2.22
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, sitting drop

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7.4

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20

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Lawrie, A.M., (1997) Nature Struct. Biol., 4, 796.

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Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein10 (mg/ml)
21drop15 (mM)
31dropHEPES10 (mM)pH7.4
41reservoir50 (mM)
51reservoirPEG400010 (%)
61reservoirHEPES0.1 (M)pH7.4

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PDB entries from 2024-04-17

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