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1RFF

Crystal structure of human Tyrosyl-DNA Phosphodiesterase complexed with vanadate, octapeptide KLNYYDPR, and tetranucleotide AGTT.

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 8.2.2
Synchrotron siteALS
Beamline8.2.2
Temperature [K]100
Detector technologyCCD
Collection date2003-02-01
DetectorADSC QUANTUM 4
Wavelength(s)1.00
Spacegroup nameP 21 21 21
Unit cell lengths50.076, 104.904, 193.832
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution50.000 - 1.700
R-factor0.19364
Rwork0.193
R-free0.21300

*

Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1jy1
RMSD bond length0.012
RMSD bond angle1.335
Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareREFMAC (5.1.24)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.760
High resolution limit [Å]1.7001.700
Rmerge0.071

*

0.482

*

Number of reflections103255
<I/σ(I)>21.042
Completeness [%]90.664.6
Redundancy4.52
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP8.2

*

298PEG 3000, NaCl, HEPES, spermine, pH 7.8, VAPOR DIFFUSION, SITTING DROP, temperature 298K
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111PEG 3000
211NaCl
311HEPES
411spermine
511H2O
612PEG 3000
712NaCl
812H2O
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein6.5 (mg/ml)
21drop250 (mM)
31dropTris15 (mM)pH8.2
41dropEDTA1 (mM)
51reservoirPEG300019-21 (%)
61reservoir200 (mM)
71reservoirspermine10 (mM)
81reservoirHEPES100 (mM)or MOPS, pH7.8

223532

PDB entries from 2024-08-07

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