issue contents

Journal logoBIOLOGICAL
CRYSTALLOGRAPHY
ISSN: 1399-0047

July 2006 issue

Highlighted illustration

Cover illustration: The figure illustrates how the crystal packing of Rna1p enabled hemihedral twinning (p. 750). Twinned crystal growth was possible owing to the presence of a twofold non-crystallographic symmetry axis almost parallel to the twin operator.

research papers


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A method has been developed for readily preparing crystals for noble-gas SAD phasing and cryopreservation and has been demonstrated with the 240-residue 26 kDa protein porcine pancreas elastase (PPE). The diffraction quality of the method is sufficiently high that a single 0.31 occupied krypton site was sufficient for SAD phasing at 1.3 Å resolution.

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The first high-resolution structure (1.1 Å resolution) of a trimethoprim-resistant plasmid-encoded R67 DHFR is described. Sheets of pentagonal networks of water molecules in the D2-symmetric active site may play a role in ligand binding, catalysis and inhibition.

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Sulfur SAD data analyses reveal that successful substructure solution and phasing is a sensitive function of choices made regarding the length of data collection and resolution cutoffs.

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The paper reports two forms of the crystal structure of a quadruple mutant (K53,56,120,121M) of PLA2. The two structures of the quadruple mutant, monoclinic and trigonal, represent the conformations of PLA2 at the lipid interface and in solution, respectively.

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The crystal structure of the human Rab protein Rab6B in its inactive (with bound MgGDP) and active (MgGTPγS-bound) forms have been determined to 2.3 and 1.8 Å, respectively. Both crystallized in space group P212121, with similar unit-cell parameters.

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The structure of the E. coli EntA protein, a bacterial member of the short-chain oxidoreductase family of enzymes, has been solved at 2.0 Å. Analysis of core residues from other family members allows the identification of active-site residues.

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An automated computational procedure for fitting a ligand into its electron density with the use of the MMFF94 force field and a Gaussian shape description has been developed.

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This case study shows that partial merohedral twinning does not hinder MIR phasing if it is recognized and the phasing and refinement procedures are adjusted accordingly. Identification of hemihedral twinning, twin correction and different refinement strategies for twinned data are discussed.



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The crystal structure of an orthorhombic form of xylanase II was determined at atomic resolution and its structural fluctuation was evaluated by analyzing the anisotropic displacement parameters.

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The first crystal structure of a C2 domain of rabphilin-3A is reported.

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High-resolution X-ray structures of human ferritin L chain in two different crystal forms revealed new insights in the mechanism of iron storage.

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The crystal structure of M. tuberculosis 1-deoxy-D-xylulose 5-phosphate reductoisomerase, with a sulfate bound in the expected site of the phosphate moiety of the sugar substrate, has been determined to 1.9 Å resolution. Structure and sequence comparisons offer suggestions for the design of specific drugs.

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The structure of the apo form of the enzyme with sulfate ions bound in the active site is presented. The structure is in a `closed' conformation relative to structures of the P. vulgaris enzyme.

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The crystal structure of 8Sα globulin of mung bean was determined at 2.65 Å resolution and its physicochemical properties were elucidated in comparison with other seed storage globulins.

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A preliminary screen has been used to maximize solubility and define buffer and salt conditions for optimal protein crystal growth of ten test proteins. A precipitant/precipitant–additive screen is also presented which is used in conjunction with the preliminary screen to define a two-step approach to crystal screening.
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