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1C9Y

HUMAN ORNITHINE TRANSCARBAMYLASE: CRYSTALLOGRAPHIC INSIGHTS INTO SUBSTRATE RECOGNITION AND CATALYTIC MECHANISM

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X12B
Synchrotron siteNSLS
BeamlineX12B
Temperature [K]298
Detector technologyIMAGE PLATE
Collection date1998-10-29
Spacegroup nameP 21 3
Unit cell lengths125.410, 125.410, 125.410
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 1.900
R-factor0.186

*

Rwork0.187
R-free0.20600

*

RMSD bond length0.012
RMSD bond angle23.960

*

Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareX-PLOR (3.851)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]35.0001.970
High resolution limit [Å]1.9001.900
Rmerge0.0590.149
Total number of observations799411

*

Number of reflections52412
<I/σ(I)>54.3
Completeness [%]99.8100
Redundancy167.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.518

*

PEG 400, AMMONIUM SULFATE, POTASSIUM CHLORIDE, EDTA, TRIS ACETATE, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 291K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein20 (mg/ml)
21dropPALO4 (mM)
31dropTris acetate20 (mM)
41dropEDTA2 (mM)
51drop20 (mM)
61reservoirPEG4002 (%)
71reservoirammonium sulfate2 (M)
81reservoirsodium HEPES0.1 (M)

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