issue contents
October 2013 issue
Cover illustration: Monoclinic casein kinase 1 (Zeringo et al., p. 1077).
scientific comment
A recently published crystallographic model of GspB in complex with a disaccharide was proposed to provide insight into the interaction of the S. gordonii adhesin with the cell sialyl-T antigen from host cells. However, a close inspection of this model revealed that in this complex a buffer molecule was mistaken for the disaccharide. As a consequence, this complex provides no information regarding the interaction of GspB with host cell receptors.
structural communications
The crystal structure of a new P21 crystal form of the catalytic domain of mammalian casein kinase 1 δ is described and compared with previously deposited structures.
PDB reference: casein kinase 1 δ, 4jjr
The recombinant production, purification, crystallization and crystal structure of 2-keto-3-deoxy-D-manno-octulosonate-8-phosphate synthase from P. aeruginosa is presented.
The crystal structure of succinyl-CoA: 3-ketoacid CoA transferase from Drosophila melanogaster was determined at 2.64 Å resolution.
PDB reference: DmSCOT, 4kgb
crystallization communications
This report describes the crystallization and X-ray diffraction analysis of the flax cytokinin oxidase LuCKX1.1.
The 155 amino-acid FP domain of the human F-box protein Fbxo7 was successfully expressed in bacteria, purified and crystallized. Native and single-wavelength anomalous dispersion data sets have been collected.
The recombinant protein of acidic thermophilic β-1,4-mannanase from Aspergillus niger BK01 was expressed, purified, and crystallized. X-ray diffraction data to 1.57 Å was collected and reported.
The cloning, expression and purification of different fragments of the S. pyogenes SpyCEP protein are reported. Preliminary X-ray diffraction analysis of a 1580-residue selenomethionine-labelled ectodomain fragment is described.
The C-terminal RNA recognition motif of human ETR-3 protein involved in myotonic dystrophy was over-expressed, purified and crystallized. The crystals obtained diffracted X-rays to 3 Å resolution and belonged to space group P213.
A putative (3R)-hydroxyacyl-CoA dehydratase, HtdX from M. tuberculosis H37Rv, has been cloned, overexpressed, purified and crystallized to collect preliminary X-ray diffraction data.
The GH42 β-galactosidase GanB from G. stearothermophilus has been crystallized in the primitive orthorhombic space group P212121. Complete diffraction data sets have been measured for the wild-type enzyme (2.45 Å resolution) and its catalytic mutant (E323A; 2.50 Å resolution) for use in a full three-dimensional structural analysis of the GanB protein.
Peptide deformylase catalyzes the deformylation of N-formylated methionine in newly synthesized polypeptides in prokaryotes and some eukaryotic organelles. The synthetic codon-optimized def gene from C. jejuni was cloned and the protein expressed, purified and crystallized. A preliminary X-ray crystallography analysis of the C. jejuni peptide deformylase crystals was performed.
Open access
A proteolytically stable fragment of a plasmid replication initiation protein from the thermophile G. stearothermophilus has been biochemically characterized, crystallized and diffraction data collected to a resolution of 2.5 Å.
A putative xylose isomerase from B. thetaiotaomicron has been crystallized (space group P1, unit-cell parameters a = 96.3, b = 101.7, c = 108.3 Å, α = 82.8, β = 68.2, γ = 83.0°). Diffraction data have been collected to 2.10 Å resolution using synchrotron X-rays.
Improvement of the expression level, crystallization and preliminary X-ray diffraction studies of D-threo-3-hydroxyaspartate dehydratase isolated from Delftia sp. HT23 are reported.
The C-terminal domain of the fibre protein from turkey adenovirus 3, a siadenovirus, consisting of amino acids 304–454, has been crystallized. Diffraction data were obtained to 2.0 and 2.14 Å resolution for a native crystal and a selenomethionine-derivative crystal, respectively.
A (2R,3R)-2,3-butanediol dehydrogenase from B. coagulans 2-6 was expressed in E. coli BL21 (DE3) and purified. Crystallization and preliminary X-ray crystallographic analysis were performed for this recombinant enzyme.
A phosphate-binding protein endowed with phosphatase activity, previously dubbed LapA, from P. aeruginosa PAO1 has been crystallized. The crystals diffracted to 0.87 Å resolution and belonged to space group P21.
A viral RNA-silencing suppressor encoded by Wuhan nodavirus has been overexpressed in Escherichia coli, purified and crystallized. Diffraction data were collected to 2.8 Å resolution.
Diffraction data were collected from a NylCp2 crystal to a resolution of 1.60 Å. The crystal belonged to space group C2221, with unit-cell parameters a = 70.84, b = 144.90, c = 129.05 Å.
The complex of Arf1-GDP and dimeric p23 peptide, which is likely to be involved in membrane binding of Arf1, has been crystallized and preliminary crystallographic analysis was performed.
Here, the purification, crystallization and preliminary X-ray crystallographic studies of the transport unit of AIDA-I are reported.
Cellobiose 2-epimerase epimerizes and isomerizes β-1,4- and α-1,4-gluco-oligosaccharides. The cellobiose 2-epimerase gene from D. turgidum was cloned and the protein was expressed, purified and crystallized. A preliminary X-ray crystallography analysis of the cellobiose 2-epimerase crystals was performed.
In this study, the B. melitensis TIR-domain-containing protein (TcpB) was cloned, expressed, purified and crystallized, and X-ray diffraction data were collected to 2.6 Å resolution.
The two Plasmodium actin isoforms were expressed, purified and crystallized in complex with the gelsolin G1 domain. Crystals diffracting to high resolution were obtained and data sets for actin I and II were collected to 1.19 and 2.2 Å resolution, respectively.
Dihydrodipicolinate synthase (DHDPS) catalyses the rate-limiting step in the biosynthesis of meso-diaminopimelate and lysine. Here, the cloning, expression, purification and crystallization of DHDPS from the intracellular pathogen Legionella pneumophila are described.
SpaA pilin, which forms the pilus shaft of SpaCBA pili in L. rhamnosus GG, was crystallized and X-ray diffraction data were collected to a resolution of 2.0 Å.
The constructed Y167H mutant α-cyclodextrin glucanotransferase was successfully expressed and purified. Single crystals were grown with two kinds of morphology in different crystallization conditions.