Human Protein-l-isoaspartate O-Methyltransferase Domain-Containing Protein 1 (PCMTD1) Associates with Cullin-RING Ligase Proteins | Biochemistry
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Molecular architecture of the augmin complex | Nature Communications
Virtual Screening Identifies Irreversible FMS-like Tyrosine Kinase 3 Inhibitors with Activity toward Resistance-Conferring Mutations | Journal of Medicinal Chemistry
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Design and Synthesis of Dual EZH2/BRD4 Inhibitors to Target Solid Tumors | Journal of Medicinal Chemistry
Fluorescence Spectroscopic Profiling of Compound Libraries | Journal of Medicinal Chemistry
From Angstroms to Nanometers: Measuring Interatomic Distances by Solid-State NMR | Chemical Reviews
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Discovery of 5-Aryl-2,4-diaminopyrimidine Compounds as Potent and Selective IRAK4 Inhibitors | ACS Medicinal Chemistry Letters
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Structure Based Drug Design of Crizotinib (PF-02341066), a Potent and Selective Dual Inhibitor of Mesenchymal–Epithelial Transition Factor (c-MET) Kinase and Anaplastic Lymphoma Kinase (ALK) | Journal of Medicinal Chemistry
Interaction of Zika Virus Envelope Protein with Glycosaminoglycans | Biochemistry
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Crystal structure of a bacterial homologue of the bile acid sodium symporter ASBT | Nature
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Discovery of Anilino-1,4-naphthoquinones as Potent EGFR Tyrosine Kinase Inhibitors: Synthesis, Biological Evaluation, and Comprehensive Molecular Modeling | ACS Omega
pH-Driven Self-Assembly of Acidic Microbial Glycolipids | Langmuir
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Tissue transglutaminase exacerbates renal fibrosis via alternative activation of monocyte-derived macrophages | Cell Death & Disease
Reactions of Amino Acids, Peptides, and Proteins with Oxidized Metabolites of Tris(p-carboxyltetrathiaaryl)methyl Radical EPR Probes | Chemical Research in Toxicology
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