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Molecular glues for targeted protein degradation: from serendipity to rational discovery
Targeted protein degradation is a promising area in the discovery and development of
innovative therapeutics. Molecular glues mediate proximity-induced protein degradation and …
innovative therapeutics. Molecular glues mediate proximity-induced protein degradation and …
Protein kinases: drug targets for immunological disorders
L Castelo-Soccio, H Kim, M Gadina… - Nature Reviews …, 2023 - nature.com
Protein kinases play a major role in cellular activation processes, including signal
transduction by diverse immunoreceptors. Given their roles in cell growth and death and in …
transduction by diverse immunoreceptors. Given their roles in cell growth and death and in …
Late-stage diversification of natural products
B Hong, T Luo, X Lei - ACS central science, 2020 - ACS Publications
Late-stage diversification of natural products is an efficient way to generate natural product
derivatives for drug discovery and chemical biology. Benefiting from the development of site …
derivatives for drug discovery and chemical biology. Benefiting from the development of site …
Multispecific drugs herald a new era of biopharmaceutical innovation
RJ Deshaies - Nature, 2020 - nature.com
The modern biopharmaceutical industry traces its roots to the dawn of the twentieth century,
coincident with marketing of aspirin—a signature event in the history of modern drug …
coincident with marketing of aspirin—a signature event in the history of modern drug …
Structural basis of lenalidomide-induced CK1α degradation by the CRL4CRBN ubiquitin ligase
Thalidomide and its derivatives, lenalidomide and pomalidomide, are immune modulatory
drugs (IMiDs) used in the treatment of haematologic malignancies,. IMiDs bind CRBN, the …
drugs (IMiDs) used in the treatment of haematologic malignancies,. IMiDs bind CRBN, the …
[HTML][HTML] Molecular glues for protein-protein interactions: Progressing toward a new dream
M Konstantinidou, MR Arkin - Cell Chemical Biology, 2024 - cell.com
The modulation of protein-protein interactions with small molecules is one of the most
rapidly develo** areas in drug discovery. In this review, we discuss advances over the …
rapidly develo** areas in drug discovery. In this review, we discuss advances over the …
Modulators of protein–protein interactions
Since Hedin's characterization of trypsin and antitrypsin in 1906,(1) arguably the first
account of a regulatory protein–protein interaction (PPI), contemporary understanding of …
account of a regulatory protein–protein interaction (PPI), contemporary understanding of …
Nucleases: diversity of structure, function and mechanism
W Yang - Quarterly reviews of biophysics, 2011 - cambridge.org
Nucleases cleave the phosphodiester bonds of nucleic acids and may be endo or exo,
DNase or RNase, topoisomerases, recombinases, ribozymes, or RNA splicing enzymes. In …
DNase or RNase, topoisomerases, recombinases, ribozymes, or RNA splicing enzymes. In …
[HTML][HTML] Serine/threonine phosphatases: mechanism through structure
Y Shi - Cell, 2009 - cell.com
The reversible phosphorylation of proteins is accomplished by opposing activities of kinases
and phosphatases. Relatively few protein serine/threonine phosphatases (PSPs) control the …
and phosphatases. Relatively few protein serine/threonine phosphatases (PSPs) control the …
Calcineurin: form and function
F Rusnak, P Mertz - Physiological reviews, 2000 - journals.physiology.org
Calcineurin is a eukaryotic Ca2+-and calmodulin-dependent serine/threonine protein
phosphatase. It is a heterodimeric protein consisting of a catalytic subunit calcineurin A …
phosphatase. It is a heterodimeric protein consisting of a catalytic subunit calcineurin A …