#1: Journal: Acta Crystallogr. Sect. F Struct. Biol. Cryst. Commun. Year: 2010 Title: Crystallization and preliminary X-ray diffraction analysis of a specific VHH domain against mouse prion protein Authors: Abskharon, R. / Soror, s. / Pardon, E. / Legname, G. / Steyaert, J. / Wohlkonig, A.
Mass: 13360.841 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Camelus dromedarius (Arabian camel) / Production host: Escherichia coli (E. coli)
Monochromator: Asymmetric Laue 001 / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelength
Wavelength: 0.933 Å / Relative weight: 1
Reflection
Resolution: 1.23→17.85 Å / Num. obs: 26127 / % possible obs: 98.19 % / Redundancy: 4.99 % / Net I/σ(I): 11.8
Reflection shell
Resolution: 1.23→1.258 Å
-
Processing
Software
Name
Version
Classification
REFMAC
5.5.0109
refinement
iMOSFLM
datareduction
SCALA
datascaling
PHASER
phasing
Refinement
Resolution: 1.23→17.85 Å / Cor.coef. Fo:Fc: 0.953 / Cor.coef. Fo:Fc free: 0.937 / SU B: 0.713 / SU ML: 0.033 / Cross valid method: THROUGHOUT / ESU R: 0.054 / ESU R Free: 0.056 / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
Rfactor
Num. reflection
% reflection
Selection details
Rfree
0.22398
1382
5 %
RANDOM
Rwork
0.19886
-
-
-
obs
0.20009
26127
98.19 %
-
Solvent computation
Ion probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.4 Å