Frontiers | The structure of MadC from Clostridium maddingley reveals new insights into class I lanthipeptide cyclases
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Targeting Her2-insYVMA with Covalent Inhibitors—A Focused Compound Screening and Structure-Based Design Approach | Journal of Medicinal Chemistry
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Targeting the Hinge Glycine Flip and the Activation Loop: Novel Approach to Potent p38α Inhibitors | Journal of Medicinal Chemistry
Allosteric Inhibitors of SHP2 with Therapeutic Potential for Cancer Treatment | Journal of Medicinal Chemistry
Structure of the heterotrimeric membrane protein complex FtsB-FtsL-FtsQ of the bacterial divisome | Nature Communications
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HheG, a Halohydrin Dehalogenase with Activity on Cyclic Epoxides | ACS Catalysis
Crystal structure of oligomeric β1-adrenergic G protein–coupled receptors in ligand-free basal state | Nature Structural & Molecular Biology
Frontiers | Structural Basis of Human Dimeric α-Amino-β-Carboxymuconate-ε-Semialdehyde Decarboxylase Inhibition With TES-1025
A dimer between monomers and hexamers—Oligomeric variations in glucosamine-6-phosphate deaminase family | PLOS ONE
Differential sensing with arrays of de novo designed peptide assemblies | Nature Communications
Structure-guided simulations illuminate the mechanism of ATP transport through VDAC1 | Nature Structural & Molecular Biology
Synthetic Multivalent Disulfide-Constrained Peptide Agonists Potentiate Wnt1/β-Catenin Signaling via LRP6 Coreceptor Clustering | ACS Chemical Biology
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Fragment-Based Ab Initio Phasing of Peptidic Nanocrystals by MicroED | ACS Bio & Med Chem Au
Biomolecules | Free Full-Text | Structural and Functional Insights into the Biofilm-Associated BceF Tyrosine Kinase Domain from Burkholderia cepacia
Computational design of constitutively active cGAS | Nature Structural & Molecular Biology
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