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1BS8

PEPTIDE DEFORMYLASE AS ZN2+ CONTAINING FORM IN COMPLEX WITH TRIPEPTIDE MET-ALA-SER

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsELLIOTT GX-18
Temperature [K]293
Detector technologyAREA DETECTOR
Collection date1998-04-15
DetectorSIEMENS-NICOLET X100
Spacegroup nameC 1 2 1
Unit cell lengths143.100, 64.200, 84.700
Unit cell angles90.00, 123.30, 90.00
Refinement procedure
Resolution6.000 - 2.200
R-factor0.204
Rwork0.204
R-free0.26100
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1icj
RMSD bond length0.011
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]20.0002.330
High resolution limit [Å]2.2002.200
Rmerge0.0800.304
Total number of observations117576

*

Number of reflections32674
<I/σ(I)>11.982
Completeness [%]99.298.4
Redundancy3.62
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

7.4Groche, D., (1998) Biochem.Biophys.Res.Comm., 246, 342.

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirammonium sulfate2 (M)
21reservoirMOPS-NH30.2 (M)
31reservoirTCEP10 (mM)
41dropPDF30 (mg/ml)
51dropformyl-Met-Ala-Ser20 (mM)
61dropammonium formate500 (mM)
71drop100 (mM)

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PDB entries from 2024-05-15

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