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8TTR

CA9 mimic bound to SH7

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAUSTRALIAN SYNCHROTRON BEAMLINE MX2
Synchrotron siteAustralian Synchrotron
BeamlineMX2
Temperature [K]100
Detector technologyPIXEL
Collection date2020-03-21
DetectorDECTRIS EIGER X 16M
Wavelength(s)0.953724
Spacegroup nameP 1 21 1
Unit cell lengths42.160, 41.514, 72.065
Unit cell angles90.00, 104.13, 90.00
Refinement procedure
Resolution40.917 - 1.450
Rwork0.163
R-free0.18660
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.011
RMSD bond angle1.835
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwarePHASER
Refinement softwareREFMAC (5.8.0415)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]41.5001.470
High resolution limit [Å]1.4501.450
Rmerge0.1662.175
Rpim0.0490.630
Number of reflections431332135
<I/σ(I)>13.41.7
Completeness [%]100.0
Redundancy12.5
CC(1/2)0.9990.556
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP8.5293CA9 mimic crystals were obtained in sitting drop plates with seeding. The protein concentration was about 5.5 mg/mL, 150 nL was added to 120 nL of reservoir and 30 nL of seeds. The reservoir consisted of 2.6 to 2.8 M ammonium sulfate with 100 mM tris buffer at pH 8.0 to 9.0

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