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5EAS

5-EPI-ARISTOLOCHENE SYNTHASE FROM NICOTIANA TABACUM

Experimental procedure
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL7-1
Synchrotron siteSSRL
BeamlineBL7-1
Temperature [K]90
Detector technologyIMAGE PLATE
Collection date1996-03
DetectorMARRESEARCH
Spacegroup nameP 41 21 2
Unit cell lengths124.730, 124.730, 118.940
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 2.250
R-factor0.24
Rwork0.240
R-free0.20000
Structure solution methodMIRAS
RMSD bond length0.007
RMSD bond angle17.900

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareVECSUM
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]25.0002.300
High resolution limit [Å]2.2502.250
Rmerge0.063

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0.275

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Total number of observations272509

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Number of reflections42946
<I/σ(I)>115.9
Completeness [%]95.296.7
Redundancy6.35.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

6.9PROTEIN WAS CRYSTALLIZED FROM 15% PEG 8000, 200 MM MG(OAC)2, 100 MM MOPSO PH 6.9, 1MM DTT; SOAKING SOLUTION FOR FREEZING ALSO INCLUDED 20% ETHYLENE GLYCOL.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirPEG800015 (%)
21reservoir200 (mM)
31reservoirMOPSO100 (mM)
41reservoirdithiothreitol1 (mM)

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PDB entries from 2024-07-03

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