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1J4A

INSIGHTS INTO DOMAIN CLOSURE, SUBSTRATE SPECIFICITY AND CATALYSIS OF D-LACTATE DEHYDROGENASE FROM LACTOBACILLUS BULGARICUS

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE X11
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineX11
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1998-12-01
DetectorMARRESEARCH
Spacegroup nameC 2 2 21
Unit cell lengths94.300, 188.000, 193.400
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution19.000 - 1.900
R-factor0.204
Rwork0.204
R-free0.25900
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)MODEL OF NATIVE D-LDH WHICH IS CURRENTLY BEING DEPOSITED IN THE PDB
RMSD bond length0.013
RMSD bond angle0.031
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]19.0001.930
High resolution limit [Å]1.9001.900
Rmerge0.0470.327
Number of reflections132348
<I/σ(I)>16.12.2
Completeness [%]98.492.4
Redundancy3.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

6.5Orthorhombic crystals were grown by vapour diffusion from solutions of 20 % PEG 6K, 0.2 M ammonium sulphate in 0.1 M cacodylate buffer pH 6.5.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirPEG600020 (%)
21reservoirammonium sulfate0.2 (M)
31reservoirsodium cacodylate0.1 (M)pH6.5

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PDB entries from 2025-06-18

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