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1HQ5

CRYSTAL STRUCTURE OF THE BINUCLEAR MANGANESE METALLOENZYME ARGINASE COMPLEXED WITH S-(2-BORONOETHYL)-L-CYSTEINE, AN L-ARGININE ANALOGUE

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RU200
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1999-10-13
DetectorRIGAKU RAXIS IIC
Wavelength(s)1.5418
Spacegroup nameP 3
Unit cell lengths91.300, 91.300, 69.400
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution20.000 - 2.300
Rwork0.158
R-free0.19400
Structure solution methodFOURIER SYNTHESIS
RMSD bond length0.007
RMSD bond angle23.300

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.380
High resolution limit [Å]2.3002.300
Rmerge0.0980.242
Total number of observations41944

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Number of reflections14462

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<I/σ(I)>8
Completeness [%]98.1

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97.5
Redundancy2.92.85
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP8.54

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drop consists of equal amounts of protein and precipitant solutions

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein10 (mg/ml)
21dropBEC3 (mM)
31drop5 (mM)
41dropbicine-NaOH25 (mM)
51reservoirPEG150024 (%)precipitant
61reservoirbicine-NaOH100 (mM)precipitant

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PDB entries from 2024-05-15

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