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4DD8

ADAM-8 metalloproteinase domain with bound batimastat

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 5.0.1
Synchrotron siteALS
Beamline5.0.1
Temperature [K]100
Detector technologyCCD
DetectorADSC QUANTUM 315r
Wavelength(s)1
Spacegroup nameP 1 21 1
Unit cell lengths91.600, 50.900, 93.500
Unit cell angles90.00, 102.40, 90.00
Refinement procedure
Resolution44.745 - 2.100
R-factor0.1916
Rwork0.188
R-free0.25500
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1r55
RMSD bond length0.008
RMSD bond angle0.682
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareMOLREP
Refinement softwarePHENIX ((phenix.refine: 1.7_650))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.180
High resolution limit [Å]2.1002.100
Number of reflections49479
<I/σ(I)>10.92.92
Completeness [%]99.395.9
Redundancy3.62.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP8291Purified ADAM-8/batimastat complex (10mg/mL) was crystallized by the sitting-drop vapor diffusion method, mixing 1uL complex with 1uL of 0.1M Tris pH 8.0, 1M sodium formate, 10% methanol. Crystals reached usable size in 10 days. Crystals were then transferred to a cryo solution containing 0.1M Tris pH 8.0, 1.2M sodium formate, 10% methanol, and 10% glycerol. The crystals were harvested and flash frozen in liquid nitrogen for data collection., VAPOR DIFFUSION, SITTING DROP, temperature 291K

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PDB entries from 2024-05-15

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