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8CMK

Transportin-3 TNPO3 in complex with RSY region of CIRBP

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsPETRA III, DESY BEAMLINE P11
Synchrotron sitePETRA III, DESY
BeamlineP11
Temperature [K]100
Detector technologyPIXEL
Collection date2021-02-05
DetectorDECTRIS EIGER2 X 16M
Wavelength(s)1.033220
Spacegroup nameP 1 21 1
Unit cell lengths97.526, 101.805, 114.133
Unit cell angles90.00, 111.13, 90.00
Refinement procedure
Resolution48.715 - 2.945
Rwork0.246
R-free0.31660
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.005
RMSD bond angle1.577
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwareMOLREP
Refinement softwareREFMAC (5.8.0403)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]48.72048.7203.060
High resolution limit [Å]2.94011.0202.940
Rmerge0.0940.0440.672
Rmeas0.1300.0610.923
Rpim0.0900.0430.629
Number of reflections435558764458
<I/σ(I)>8
Completeness [%]98.5
Redundancy3.53.33.5
CC(1/2)0.9960.9950.509
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP277.150.5ul Protein (TNPO3) 12mg/ml with 0.2ul Ligand (CIRBP) 4.4mg/ml and 0.1ul seeding stock were mixed with 0.5ul of condition. Condition: 0.1M Sodium HEPES, 0.1M MOPS (acid), 7.5pH, 12.5% v/v MPD; 12.5% PEG 1000; 12.5% w/v PEG 3350, 0.05% w/v D-Salicin, 0.05% w/v Esculin hydrate, 0.05% w/v Quinine hemisulfate salt monohydrate, 0.05% w/v Tryptamine, 0.05% w/v Arbutin (in 50% EtOH) Protein and Ligand in 50mM Tris, 150mM NaCl, 2mM TCEP, 0.04% NaN3, pH: 7.5 Buffer

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