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7XSV

Crystal Structures of PIM1 in Complex with Macrocyclic Compound H3

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRF BEAMLINE BL10U2
Synchrotron siteSSRF
BeamlineBL10U2
Temperature [K]291
Detector technologyPIXEL
Collection date2022-01-24
DetectorDECTRIS EIGER X 16M
Wavelength(s)0.9792
Spacegroup nameP 65
Unit cell lengths97.111, 97.111, 78.955
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution31.790 - 2.660
R-factor0.1969
Rwork0.193
R-free0.23320
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)6kzi
Data reduction softwareXDS (Feb 5, 2021)
Data scaling softwareAimless (0.7.7)
Phasing softwarePHASER (2.8.3)
Refinement softwarePHENIX (1.19.2)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]41.36041.3602.790
High resolution limit [Å]2.6608.8102.660
Rmerge0.1520.0561.626
Rmeas0.1560.0581.669
Rpim0.0350.0140.372
Total number of observations223541520131485
Number of reflections115583511580
<I/σ(I)>1640.12.4
Completeness [%]93.798.996.8
Redundancy19.314.819.9
CC(1/2)0.9990.9980.681
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP82910.4M POTASSIUM SODIUM TARTRATE

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