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1HNK

CRYSTAL STRUCTURE OF BETA-KETOACYL-ACP SYNTHASE III, APO TETRAGONAL FORM

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 17-ID
Synchrotron siteAPS
Beamline17-ID
Temperature [K]100
Detector technologyCCD
Collection date2000-01-01
DetectorMARRESEARCH
Wavelength(s)1
Spacegroup nameP 41 21 2
Unit cell lengths72.650, 72.650, 99.780
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 1.900
Rwork0.204
R-free0.24000
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)1hn9
RMSD bond length0.012
RMSD bond angle1.500
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.970
High resolution limit [Å]1.9001.900
Rmerge0.060

*

0.580
Total number of observations303763

*

Number of reflections40226

*

<I/σ(I)>2.5
Completeness [%]99.9100
Redundancy88
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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PDB entries from 2024-12-25

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