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1QA0

BOVINE TRYPSIN 2-AMINOBENZIMIDAZOLE COMPLEX

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RU300
Temperature [K]298
Detector technologyIMAGE PLATE
Collection date1994-10-10
DetectorRIGAKU RAXIS II
Spacegroup nameP 31 2 1
Unit cell lengths55.020, 55.020, 109.140
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution10.000 - 1.800
R-factor0.172
Rwork0.172
RMSD bond length0.017
RMSD bond angle0.033
Data scaling softwareSCALEPACK
Refinement softwarePROFFT
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]10.0001.900
High resolution limit [Å]1.8001.800
Rmerge0.0950.026

*

Number of reflections16893
<I/σ(I)>8.1
Completeness [%]91.178.5
Redundancy6.34
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.4298MICROCRYSTALS WERE INITIALLY GROWN USING THE HANGING DROP METHOD IN LINBRO CULTURE PLATES. CRYSTALLIZATION RESERVOIRS CONTAIN 1.8 - 2.0 M AMMONIUM SULFATE, 50 MM TRIS HCL, 10 MM CACL2, PH 7.4. SIX UL OF 15 MG/ML BOVINE TRYPSIN IN 20 MM 2-AMINOBENZIMIDAZOLE WAS ADDED TO 6 UL OF RESERVOIR. MACROSEEDING WAS USED TO GROW LARGE CRYSTALS (REF 2). SINGLE CRYSTALS WERE WASHED IN 0.8 M AMMONIUM SULFATE, 50 MM TRIS HCL, 10 MM CACL2, PH 7.4. THE WASHED CRYSTALS WERE PLACED IN A 18 HOUR OLD HANGING., VAPOR DIFFUSION, HANGING DROP, temperature 298K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirammonium sulfate1.8-2.0 (M)
21reservoirTris-HCl50 (mM)
31reservoir10 (mM)
41droptrypsin15 (mg/ml)
51drop2-aminobenzimidazole20 (mM)

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