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1LSH

LIPID-PROTEIN INTERACTIONS IN LIPOVITELLIN

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-ID
Synchrotron siteAPS
Beamline19-ID
Temperature [K]100
Detector technologyCCD
Collection date1998-02-07
DetectorCUSTOM-MADE
Wavelength(s)1.0332
Spacegroup nameC 1 2 1
Unit cell lengths190.170, 84.520, 89.530
Unit cell angles90.00, 100.39, 90.00
Refinement procedure
Resolution30.000

*

- 1.900
R-factor0.193
Rwork0.193
R-free0.25500
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)LIPOVITELLIN (ROOM TEMP)
RMSD bond length0.019
RMSD bond angle2.500
Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS (1.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0001.990
High resolution limit [Å]1.9001.900
Rmerge0.064

*

Number of reflections82007
<I/σ(I)>12.2
Completeness [%]74.430.1
Redundancy1.54
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.218

*

Protein stock:10 mg/ml lipovitellin, 0.25 mM sodium citrate; Well: 0.55-0.61 M sodium citrate, 1mM thioglycerol, 1 mM EDTA, 0.05% sodium azide, pH 6.2, VAPOR DIFFUSION, HANGING DROP, temperature 291K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein10 (mg/ml)
21dropsodium citrate0.25 (M)pH6.2
31reservoirsodium citrate0.55-0.61 (M)pH6.2
41reservoirthioglycerol1 (mM)
51reservoirEDTA1 (mM)
61reservoirsodium azide0.05 (%)

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PDB entries from 2024-05-15

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