Title

..., Saulius Grazulis1, ...

1 Institute of Biotechnology, Graiciuno 8, LT-02241 Vilnius, Lithuania

Abstract

Introduction

Overall structure

Coordinates and structure factors are deposited under PDB ID xxxx.

Catalytic domain

DNA-binding domain

DNA recognition and cleavage

Discussion

Materials and methods

Protein purification and crystallisation

Data collection and structure determination

References

Acknowledgments

Tables

Table 1. Data collection and refinement statistics

Dataset:	L28B2 (native)
Temperature	
Spacegroup	
a=b=, Å c=, Å	
Resolution, Å (final shell)	
Reflections unique (total)	
Completeness (%) overall (final shell)	
I/I overall (final shell)	
Rmerge overall	
Number of heavy atom sites	
Phasing power (centric/acentric)	
FOM (MIR)	
Refinement statistics:
Dataset:	
Number of atoms	
Number of solvent molecules	
Number of bounded buffer molecule atoms	
Test set size	
Rcryst (Rfree)	
RMS bonds/angles	
Average B-factors (Å2) main chain side chains solvent cofactors	

cwhereis an intensity value of i­th measurement of reflection h,, sumruns over all measured reflections, and is an average measured intensity of the reflection h. Number nh is a number of measurements of reflection h.

dRiso=h|Fp-Fph|/h|Fp|, where Fp and Fph are native and derivative structure factors, respectively.

eRCullis=h|Fh(obs)-Fh(calc)|/h|Fh(obs)|

fPhasing power=<|Fh(obs)|>/r.m.s.d., where  is lack of closure.

l

Figure legends

Fig. 1

ver. 801 Saulius Grazulis 2009-05-07

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Saulius Grazulis

2003-05-27T16:13:41