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1HND

CRYSTAL STRUCTURE OF BETA-KETOACYL-ACP SYNTHASE III-COA COMPLEX

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 17-ID
Synchrotron siteAPS
Beamline17-ID
Temperature [K]100
Detector technologyCCD
Collection date1999-04-01
DetectorMARRESEARCH
Wavelength(s)1
Spacegroup nameP 41 21 2
Unit cell lengths72.510, 72.510, 102.450
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 1.600
Rwork0.213
R-free0.25700
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)FabH-AcCoA complex
RMSD bond length0.014
RMSD bond angle1.700
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.660
High resolution limit [Å]1.6001.600
Rmerge0.1300.250
Total number of observations166321

*

Number of reflections29689
<I/σ(I)>2
Completeness [%]81.035
Redundancy66
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

7.4

*

Janson, C.A., (2000) Acta Crystallogr.D, 56, 747.

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein10 (mg/ml)
21dropTris-HCl20 (mM)
31drop50 (mM)
41dropdithiothreitol2 (mM)
51reservoirmagnesium chloride0.1 (M)
61reservoirTris-HCl0.05 (M)
71reservoirPEG400015 (%)

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