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1PN0

Phenol hydroxylase from Trichosporon cutaneum

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE BW7B
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineBW7B
Temperature [K]100
Detector technologyAREA DETECTOR
Collection date2001-06-17
DetectorMARRESEARCH
Wavelength(s)0.8452
Spacegroup nameP 1 21 1
Unit cell lengths99.999, 150.948, 114.962
Unit cell angles90.00, 114.63, 90.00
Refinement procedure
Resolution20.000

*

- 1.700
R-factor0.15698
Rwork0.157
R-free0.17990

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Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)PDB ID ENTRY 1FOH
RMSD bond length0.012
RMSD bond angle1.400

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Refinement softwareREFMAC (5.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.700
High resolution limit [Å]1.6801.680
Rmerge0.033

*

0.256

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Number of reflections2979003440

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<I/σ(I)>232.2
Completeness [%]83.938.7
Redundancy2.10.77
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

8.5

*

4

*

Enroth, C., (1994) J.Mol.Biol., 238, 128.

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Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropenzyme20 (mg/ml)
21dropphenol20 (mM)
31reservoirTris-HCl120 (mM)or 0.21M KCl and 16% PEG4000
41reservoirammonium acetate0.52 (M)

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