Table 2 PcVps75ΔCM-SeMet data collection and refinement statistics

From: Structural basis for the acetylation of histone H3K9 and H3K27 mediated by the histone chaperone Vps75 in Pneumocystis carinii

PcVps75ΔCM-SeMet

Data collection

Wavelength (Å)

0.9785

Space group

P2 1 2 1 2

Unit-cell parameters (Å, °)

a = 141.7, b = 76.4, c = 130.5;

α = β = γ = 90.0

Resolution (Å)

50.00–2.09 (2.13–2.09)

Rmergea (%)

8.4 (56.7)

Average I/σ(I)

23.8 (3.8)

No. of observed reflections

1.111,487 (1147)

No. of unique reflections

159,739 (56,203)

Completeness (%)

100 (100)

Redundancy

7.0 (7.0)

Matthews coefficient (Å3 Da−1)

2.54

Solvent content (%)

51.52

Molecules per asymmetric unit

6

Refinement

Resolution (Å)

48.26–2.09

Rwork/Rfree

0.19/0.24

Ramachandran favored (%)

95.87

Ramachandran allowed (%)

4.13

Ramachandran outliers (%)

0

No. of atoms

Protein

10342

Ligand/ion

43/12

Water

232

Wilson B value

37.82

R.m.s. deviations

Bond lengths (Å)

0.008

Bond angles (°)

1.085

  1. aRmerge= \(\mathop {\sum}\nolimits_{hkl} {\mathop {\sum}\nolimits_i {\left| {I_i\left( {hkl} \right) - \left\langle {I\left( {hkl} \right)} \right\rangle } \right|/\mathop {\sum}\nolimits_{hkl} {\mathop {\sum}\nolimits_i {I_i(hkl)} } } }\), where Ii (hkl) is an individual intensity measurement, and \(\left\langle {I\left( {hkl} \right)} \right\rangle\) is the average intensity for all i reflections
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