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1BS7

PEPTIDE DEFORMYLASE AS NI2+ CONTAINING FORM

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsELLIOTT GX-18
Temperature [K]293
Detector technologyAREA DETECTOR
Collection date1997-01-15
DetectorSIEMENS-NICOLET X100
Spacegroup nameC 1 2 1
Unit cell lengths143.400, 64.000, 84.500
Unit cell angles90.00, 123.00, 90.00
Refinement procedure
Resolution6.000 - 2.500
R-factor0.203
Rwork0.203
R-free0.27200
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1icj
RMSD bond length0.013
RMSD bond angle1.300
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwareX-PLOR (3.851)
Refinement softwareX-PLOR (3.851)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.640
High resolution limit [Å]2.5002.500
Rmerge0.0860.329
Number of reflections21929
<I/σ(I)>13.32.42
Completeness [%]97.294.4
Redundancy4.13.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1unknown

*

7.4SEE: D.GROCHE,A.BECKER,I.SCHLICHTING,W.KABSCH, S.SCHULTZ,A.F.V.WAGNER (1998) BIOCHEM.BIOPHYS.RES.COMM. 246, 342, pH 7.4
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
111ammonium sulfate2 (M)
211PEG10001 (%(w/v))

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