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1URX

Crystallographic structure of beta-agarase A in complex with oligoagarose

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-1
Synchrotron siteESRF
BeamlineID14-1
Temperature [K]193
Collection date2003-03-15
Spacegroup nameP 32 2 1
Unit cell lengths51.380, 51.380, 205.360
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution37.200 - 1.700
R-factor0.15642
Rwork0.155
R-free0.18200

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Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1o4y
RMSD bond length0.015

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RMSD bond angle1.762

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Data reduction softwareDENZO
Data scaling softwareSCALA
Phasing softwareAMoRE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]37.2001.760
High resolution limit [Å]1.7001.700
Rmerge0.0420.110
Total number of observations148960

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Number of reflections34045
<I/σ(I)>12.16.8
Completeness [%]95.398.4
Redundancy4.44.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.5

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20.5

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30 % PEG 4000 200 MM AMMONIUM ACETATE, 100 MM SODIUM ACETATE PH 4.6
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein3.5 (mg/ml)
21dropTris50 (mM)pH7.5
31drop25 (mM)
41dropagaro-octaose4 (mM)
51reservoirPEG400030 (%)
61reservoirammonium acetate200 (mM)
71reservoirsodium acetate100 (mM)pH4.6

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