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1NH3

Human Topoisomerase I Ara-C Complex

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X12B
Synchrotron siteNSLS
BeamlineX12B
Temperature [K]100
Detector technologyCCD
Collection date2001-02-18
DetectorMARRESEARCH
Wavelength(s)1.1
Spacegroup nameP 32
Unit cell lengths72.970, 72.970, 186.290
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution100.000

*

- 3.100
R-factor0.235
Rwork0.235
R-free0.24300

*

Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1a31
RMSD bond length0.012

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RMSD bond angle1.550

*

Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]100.000

*

3.210
High resolution limit [Å]3.1003.100
Rmerge0.135

*

0.415

*

Total number of observations169504

*

Number of reflections13878
Completeness [%]69.354.7
Redundancy12.2

*

Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.722

*

Redinbo, M.R., (1998) Science, 279, 1504.

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropPEG4008 (%)
21drop33.3 (mM)
31dropTris35.5 (mM)
41dropdithiothreitol4.4 (mM)
51dropwater0.003ml
61dropoligo0.01 (mM)
71drop0.7 (mM)
81dropprotein1 (mg/ml)
91dropEDTA0.2 (mM)

227344

PDB entries from 2024-11-13

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