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4NIV

Crystal structure of trypsiligase (K60E/N143H/Y151H/D189K trypsin) trigonal form

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsBESSY BEAMLINE 14.2
Synchrotron siteBESSY
Beamline14.2
Wavelength(s)0.9184
Spacegroup nameP 31 2 1
Unit cell lengths54.510, 54.510, 107.082
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution19.688 - 1.000
R-factor0.1513
Rwork0.150
R-free0.17290
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.005
RMSD bond angle1.153
Data scaling softwareXSCALE
Phasing softwarePHASER
Refinement softwarePHENIX (1.8_1069)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]19.68820.0001.100
High resolution limit [Å]1.00010.0001.000
Rmerge0.0510.0580.420
Number of reflections8876511213721
<I/σ(I)>21.0848.192.7
Completeness [%]88.698.255.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.42930.1 M HEPES/NaOH, 20% (w/v) polyethyleneglycol 4000, pH 7.4, VAPOR DIFFUSION, HANGING DROP, temperature 293K

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