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1KNR

L-aspartate oxidase: R386L mutant

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-2
Synchrotron siteESRF
BeamlineID14-2
Temperature [K]100
Detector technologyCCD
Collection date2001-02-12
DetectorMARRESEARCH
Wavelength(s)0.93
Spacegroup nameP 41 21 2
Unit cell lengths73.278, 73.278, 313.933
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution40.000 - 2.500
R-factor0.248

*

Rwork0.250
R-free0.29500

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RMSD bond length0.022
RMSD bond angle2.600

*

Data reduction softwareMOSFLM
Data scaling softwareCCP4 ((SCALA))
Phasing softwareAMoRE
Refinement softwareREFMAC (5.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.565
High resolution limit [Å]2.5002.500
Rmerge0.1070.373

*

Total number of observations68503

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Number of reflections26873
<I/σ(I)>4.71.2
Completeness [%]96.196.4
Redundancy2.32.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP8

*

22

*

isopropanol, Hepes, sodium citrate, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirHEPES-KOH100 (mM)pH7.5
21reservoirsodium citrate100 (mM)pH7.5
31reservoir2-propanol4-8 (%(v/v))
41dropprotein50 (mg/ml)
51dropHEPES-KOH50 (mM)pH8.0

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PDB entries from 2024-05-15

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