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. Author manuscript; available in PMC: 2012 Apr 16.
Published in final edited form as: J Biol Chem. 2005 Apr 4;280(24):23000–23008. doi: 10.1074/jbc.M501534200

Table 1.

Crystallographic statistics for data collected on native and selenomethionine ArnA decarboxylase and formyltransferase domains

ArnA decarboxylase domain ArnA formyltransferase domain
Data collection
Peak Inflection Remote Native Peak Inflection Remote Native
Resolution (Å) 61-3.35 88-2.30 24-1.6 28-1.2
Highest shell (Å) 3.43-3.35 2.42-2.30 1.63-1.6 1.26-1.2
Wavelength (Å) 0.9798 0.9710 0.9392 0.933 0.9793 0.9796 0.9393 0.934
Unique reflections 15066 15065 15047 25245 77800 77914 77900 183672
Multiplicity 65
(67)
21
(21)
21
(21)
16.3
(11.4)
4.4
(4.5)
4.4
(4.5)
4.3
(4.4)
4.9
(4.9)
Completeness (%) 100
(100)
100
(100)
100 (100) 97.8
(100)
96.8
(95.8)
96.9
(95.8)
96.8
(95.8)
98.3
(98.3)
Rmerge (%) 14.3
(31.1)
12.4
(27.1)
13.4
(29.7)
7.0
(36.9)
5.1
(11.5)
5.1
(11.3)
5.1
(11.3)
6.2
(29.7)
I/σ 4.4
(2.2)
4.7
(1.5)
5.3
(2.5)
7.8
(2.1)
8.8
(6.3)
8.9
(6.2)
8.8
(6.2)
7
(2.4)
Structure
solution
Monomers in a.u. 1 2
Se sites 4 8
z-score 13.8 21.3
Phasing power 0.52 0.64
Refinement
Rmsd2 bond length
(Å)/angles (°)
0.019/1.63 0.019/1.93
Rfactor/RFREE(%) 18.6/23.0
(21.1/26.5)
13.5/15.7
(14.4/18.2)
Residues in most
favored regions3
(%)
90 92
Residues in
allowed regions3
(%)
10 8
PDB code 2b11 2bln
1

Numbers in parenthesis correspond to highest resolution shell.

2

Rmsd root mean square deviation

3

These refer to the Ramachandran plot and are defined by PROCHECK (49).