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1EB8

Structure Determinants of Substrate Specificity of Hydroxynitrile Lyase from Manihot esculenta

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE X11
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineX11
Temperature [K]100
Detector technologyIMAGE PLATE
DetectorMARRESEARCH
Spacegroup nameP 41 21 2
Unit cell lengths106.400, 106.400, 188.430
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution8.000 - 2.100
R-factor0.192
Rwork0.192
R-free0.23400
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1dwp
RMSD bond length0.015
RMSD bond angle24.200

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareX-PLOR (3.851)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.170
High resolution limit [Å]2.1002.100
Rmerge0.0420.141
Total number of observations254472

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Number of reflections63450
<I/σ(I)>21.15.2
Completeness [%]99.999.4
Redundancy4.54.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

5.4293

*

Lauble, H., (1999) Acta Crystallogr.,Sect.D, 55, 904.

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Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirPEG80005 (%)
21reservoirMPD16 (%)
31reservoirsodium citrate100 (mM)pH5.4
41dropprotein32 (mg/ml)
51dropsodium citrate10 (mM)pH5.4

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PDB entries from 2024-05-15

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