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1AOH

SINGLE COHESIN DOMAIN FROM THE SCAFFOLDING PROTEIN CIPA OF THE CLOSTRIDIUM THERMOCELLUM CELLULOSOME

Experimental procedure
Source typeSYNCHROTRON
Source detailsLURE BEAMLINE DW32
Synchrotron siteLURE
BeamlineDW32
Temperature [K]110
Detector technologyIMAGE PLATE
Collection date1996-11
DetectorMARRESEARCH
Spacegroup nameP 21 21 21
Unit cell lengths37.840, 80.500, 93.240
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution10.000 - 1.700
R-factor0.194
Rwork0.194
R-free0.26000

*

Structure solution methodMIR
RMSD bond length0.014
RMSD bond angle28.240

*

Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR (3.1)
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.760
High resolution limit [Å]1.7001.700
Rmerge0.0550.253
Total number of observations175259

*

Number of reflections29669
<I/σ(I)>22.24.5
Completeness [%]92.286.6
Redundancy5.83.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

6.25Beguin, P., (1996) Protein Sci., 5, 1192

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirPEG800018 (%(w/v))
21reservoircalcium acetate0.2 (M)
31reservoirglycerol6 (%(v/v))
41reservoirsodium cacodylate0.05 (M)
51dropPEG80009 (%(w/v))
61dropcalcium acetate0.1 (M)
71dropglycerol3 (%(v/v))
81dropsodium cacodylate0.025 (M)pH6.25
91dropprotein7.5-10 (mg/ml)

238268

PDB entries from 2025-07-02

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