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1DC1

RESTRICTION ENZYME BSOBI/DNA COMPLEX STRUCTURE: ENCIRCLEMENT OF THE DNA AND HISTIDINE-CATALYZED HYDROLYSIS WITHIN A CANONICAL RESTRICTION ENZYME FOLD

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RU200
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1998-09-01
DetectorRIGAKU RAXIS
Spacegroup nameP 21 21 21
Unit cell lengths80.294, 87.823, 99.454
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution8.000 - 1.700
R-factor0.19
Rwork0.190
R-free0.25300
Structure solution methodMIR
RMSD bond length0.010
RMSD bond angle1.600
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR
Refinement softwareX-PLOR (3.851)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0001.760
High resolution limit [Å]1.7001.700
Rmerge0.0590.519
Number of reflections77509
<I/σ(I)>24.52.1
Completeness [%]99.495.4
Redundancy3.72.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.6293EQUILIBRATION AGAINST RESERVOIR OF 20% (V/V) DIOXANE, 2% (V/V) ETHYLENE GLYCOL AND 5 MM DTT. DROPS WERE FORMED BY MIXING 2.5 UL PROTEIN-DNA COMPLEX (10 MG/ML PROTEIN; 1.1 FOLD MOLAR EXCESS DNA) IN BUFFER (20 MM TRIS-HCL PH 7.6, 300 MM NACL, 0.1 MM EDTA, 1 MM DTT, 0.02% NA AZIDE) WITH 2.5 UL DISTILLED WATER, 2.5 UL RESERVOIR SOLUTION AND 1.5 UL 350 MM N-HEPTYL-B-D-GLUCOSIDE, VAPOR DIFFUSION, HANGING DROP, temperature 293.0K
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111TRIS HCL
1012DIOXANE
1112ETHYLENE GLYCOL
211NACL
311EDTA
411N-HEPTYL-B-D-GLUCOSIDE
511NAN3
611DTT
711DIOXANE
811ETHYLENE GLYCOL
912DTT
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein9.3 (mg/ml)
21reservoirp-dioxane20 (%(v/v))
31reservoirethylene glycol2 (%(v/v))
41reservoirdithiothreitol5 (mM)
51dropn-heptyl-beta-D-glucoside350 (mM)

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