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Nature Chemistry is a unique forum for chemists of all disciplines. Every month Nature Chemistry publishes original top-quality research, plus a compelling mix of news and reviews, in print and online.

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Reply to: Macrocyclic colibactins

Nature Chemistry, Published online: 21 September 2020; doi:10.1038/s41557-020-00552-7Reply to: Macrocyclic colibactins

The catalytic dwell in ATPases is not crucial for movement against applied torque

Nature Chemistry, Published online: 21 September 2020; doi:10.1038/s41557-020-0549-6Despite the fundamental role of ATPase in catalysing ATP hydrolysis, the structural and energetic aspects of this process are not fully understood. Coarse-grained computational models have now been used to calculate the free-energy surfaces of different types of ATPases....

Chemistry’s got talent

Nature Chemistry, Published online: 21 September 2020; doi:10.1038/s41557-020-00556-3Manza B. J. Atkinson talks to Nature Chemistry about his path to become a chemist, and how he applies the scientific method to all aspects of his life — from financial analysis to coaching youth sports teams.

Macrocyclic colibactins

Nature Chemistry, Published online: 21 September 2020; doi:10.1038/s41557-020-00551-8Macrocyclic colibactins

Quantum machine learning using atom-in-molecule-based fragments selected on the fly

Nature Chemistry, Published online: 14 September 2020; doi:10.1038/s41557-020-0527-zQuantum machine learning with improved data efficiency and transferability has been achieved using on-the-fly selection of query-dependent training molecules, which are drawn from a ‘dictionary’ of atom-in-molecule-based fragments. The benefits of the resulting models...

One-pot, room-temperature conversion of dinitrogen to ammonium chloride at a main-group element

Nature Chemistry, Published online: 14 September 2020; doi:10.1038/s41557-020-0520-6The vast majority of species capable of converting dinitrogen to ammonia rely on transition metals. Now, a boron compound has been shown to mediate the one-pot binding, cleavage and reduction of N2 to ammonium salts under mild conditions through a complex cascade mechanism...

Lysine acylation using conjugating enzymes for site-specific modification and ubiquitination of recombinant proteins

Nature Chemistry, Published online: 14 September 2020; doi:10.1038/s41557-020-0528-yA chemoenzymatic method to site-specifically conjugate peptide and protein thioesters to folded proteins at lysine residues has been developed. The method uses a genetically encoded four-residue tag that is recognized by the E2 SUMO-conjugating enzyme Ubc9. This approach...

Quantum machine learning using atom-in-molecule-based fragments selected on the fly

One-pot, room-temperature conversion of dinitrogen to ammonium chloride at a main-group element

Lysine acylation using conjugating enzymes for site-specific modification and ubiquitination of recombinant proteins

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