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1OFC

nucleosome recognition module of ISWI ATPase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-4
Synchrotron siteESRF
BeamlineID14-4
Temperature [K]100
Detector technologyCCD
Collection date2002-10-13
DetectorADSC CCD
Spacegroup nameC 1 2 1
Unit cell lengths109.470, 66.340, 82.830
Unit cell angles90.00, 124.41, 90.00
Refinement procedure
Resolution19.000

*

- 1.900
R-factor0.21946
Rwork0.218
R-free0.25300

*

Structure solution methodMAD
RMSD bond length0.019

*

RMSD bond angle1.701

*

Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwareSOLVE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]19.000

*

2.000
High resolution limit [Å]1.9001.900
Rmerge0.0480.300
Total number of observations141793

*

Number of reflections382755452

*

<I/σ(I)>14.84.1
Completeness [%]98.699.1
Redundancy3.73.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

7.6

*

20

*

1MUL PROTEIN AT 60MG/ML IN 20MM HEPES, 0.5M NACL, PH 7, WAS MIXED WITH 4MUL, 0.125M HEPES PH 7.0, 5% PEG 6000 RESERVOIR 0.1M HEPES, 4% PEG 6000, 0.1M NACL CRYSTALS GROWTH INDUCED BY MICRO SEEDING
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirPEG60004 (%)
21reservoirHEPES0.1 (M)pH7.0
31dropTris-Cl50 (mM)pH7.6
41drop100 (mM)
51dropglycerol50 (%)

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PDB entries from 2024-07-17

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