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1J8V

Crystal structure of barley beta-D-glucan glucohydrolase isoenzyme Exo1 in complex with 4'-nitrophenyl 3I-thiolaminaritrioside

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsMACSCIENCE
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date2000-12-12
DetectorRIGAKU RAXIS II
Wavelength(s)1.5418
Spacegroup nameP 43 21 2
Unit cell lengths100.533, 100.533, 181.959
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution10.000 - 2.400
R-factor0.2008

*

Rwork0.201
R-free0.24960

*

Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ieq
RMSD bond length0.010
RMSD bond angle1.300
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.00050.000
High resolution limit [Å]2.4002.400
Rmerge0.0870.274
Total number of observations176916

*

Number of reflections34896
<I/σ(I)>7.8
Completeness [%]93.985.5
Redundancy5.18
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7277-279

*

Hrmova, M., (1998) Acta Cryst., D54, 687.

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropenzyme6.8 (mg/ml)
21dropHEPES-NaOH75 (mM)
31dropsodium acetate7.5 (mM)
41dropPEG4001.2 (%(w/v))
51dropammonium sulfate0.8 (M)
61reservoirammonium sulfate1.7 (M)
71reservoirHEPES-NaOH50 (mM)

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PDB entries from 2024-11-06

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