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With the progression of our understanding of HDL particles, multiple protein molecules that coisolate with HDL have attracted great attention [ 7].
Our sDectin-1 chemical cross-linking data suggest that similar or identical N-glycan structures are expressed on multiple protein molecules in tumor cells as Dectin-1 ligands.
The distinction is that amyloid fibrils are formed by strands from multiple protein molecules, whereas here a single protein forms the sheet.
In eukaryotes, several ribosomes can bind to an mRNA molecule at the same time, as polysomes, and multiple protein molecules can be synthesized from a single mRNA at the same time.
Although the methodology may be easily extended to include the prediction of ligands that interact with multiple protein molecules, for simplicity we only considered structures in which the ligand interacts with a single protein molecule.
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By combining automated immunofluorescent staining and tried-and-true method of reconstructing adjacent sections, we were able to visualize, in detail, not only the geometric structures of the sample but also the presence and interactions of multiple proteins and molecules of interest within their 3-dimensional environment.
The self-organization of the ribosome from multiple protein and RNA molecules and the formation of Buckminsterfullerene via the condensation of vaporized carbon are the examples of noncovalent and covalent self-assemblies, respectively, and are fundamentally distinct from the instances of architectural self- construction.
The fast relative mobility of these complexes suggests that they contain one or maximally two Ss-LrpB dimers, rather than multiple cooperatively binding protein molecules.
Therefore, the observed patterns of epistasis and compensation do not merely reflect the robustness of individual RNA and protein molecules to multiple mutations (as described above), but must indicate more general features of their genomes.
These extracellular vesicles have a lipid bilayer structure, and carry multiple proteins and RNA molecules [ 10].
Due to the inherent promiscuity of many molecules in binding to multiple protein targets, plurality of bioactivities must be considered when building models to predict the protein targets or pharmacological activities of small organic compounds.
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several protein molecules
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various protein molecules
many protein molecules
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multiple signaling molecules
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