issue contents

Journal logoSTRUCTURAL BIOLOGY
COMMUNICATIONS
ISSN: 2053-230X

October 2013 issue

Highlighted illustration

Cover illustration: Monoclinic casein kinase 1 [delta] (Zeringo et al., p. 1077).

scientific comment


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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


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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.

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The recombinant production, purification, crystallization and crystal structure of 2-keto-3-deoxy-D-manno-octulosonate-8-phosphate synthase from P. aeruginosa is presented.

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The crystal structure of succinyl-CoA: 3-ketoacid CoA transferase from Drosophila melanogaster was determined at 2.64 Å resolution.

crystallization communications


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This report describes the crystallization and X-ray diffraction analysis of the flax cytokinin oxidase LuCKX1.1.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.


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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.

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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.

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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.

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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.

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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.

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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.
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