issue contents

Journal logoSTRUCTURAL BIOLOGY
COMMUNICATIONS
ISSN: 2053-230X

November 2026 issue

Highlighted illustration

Cover illustration: The crystal structure of phosphoribosyl isomerase A from Mycobacterium tuberculosis (mtPriA) was determined with a bound light-controllable 1,2-dithienylethene inhibitor (DTE LC6) at a resolution of 1.95 Å, explaining the previously reported inhibitory effect of DTE LC6 on the catalytic activity of mtPriA [Rajendran & Sterner (2026), Acta Cryst. F82, 385–390].

early career research


research communications


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The crystal structure of H. pylori MurI is reported at 1.43 Å resolution.

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We have determined the crystal structure of an isomerase catalyzing two steps in histidine and tryptophan biosynthesis with a bound light-switchable competitive inhibitor. The work explains the mode of action of the inhibitor and describes the discovery of a hitherto unknown third phosphate-binding site of the enzyme.

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For the first time, the recombinant core botulinum neurotoxin type A (BoNT/A) expressed in Escherichia coli and nicked in vitro is shown to be structurally identical to native BoNT/A from Clostridium botulinum, enabling direct activity comparison between the recombinant product and the native toxin.

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Crystal structures of the SARS-CoV-2 N protein N-terminal domain and C-terminal domain determined at resolutions of 1.30–1.94 Å reveal a conserved N-terminal domain fold containing a positively charged cleft encompassing residues previously implicated in RNA binding and a conserved β-hairpin-mediated C-terminal domain dimer.

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Nijmegen breakage syndrome 1 (NBS1), a component of the MRE11–RAD50–NBS1 complex, plays a key role in the repair of DNA double-strand breaks. We report the first experimentally determined X-ray crystal structure of the FHA–BRCT region of human NBS1 and the results of docking simulations of candidate radiosensitizing compounds.

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The GloB cupin domain from an unknown biosynthetic gene cluster from P. aeruginosa shows similarities to isomerase enzymes.