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Usually the structure of small molecules cannot be deduced from the genomic sequence.
The interactions between DSAI and wild-DNA are rather strong, thus DSAI molecules cannot be hauled out from wild-DNA and the fluorescence stays still.
This is reflected at the cellular level where receptors and signalling molecules cannot be identified using standard homology-based searches querying with proteins from prokaryotes and other eukaryotes.
A major challenge in this technique is to ensure that measurements reflect bonds between single biomolecules because the molecules cannot be directly observed.
Therefore, when the R6G concentration is equal to or less than 10−4 M, peaks associated to R6G molecules cannot be detected in the Raman measurement.
Although systematic use of these molecules cannot be advocated, several areas of uncertainty remain, including potential benefits in patients with more severe illness or in specific subgroups.
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These results indicate that the PF molecule cannot be released to DNA without introducing external stimulus.
When a molecule cannot be extended any further, the recursion is terminated and the program backtracks in the search tree.
No one thinks, for example, that because an individual H2O molecule cannot be seen, it is therefore unintelligible to speak of the molecule's shape.
In View mode, the molecule cannot be changed, so mouse behavior is limited to rotation of the entire molecule or selecting atoms to provide information.
We then show that a refactored pathway must produce thiamin itself rather than a stripped-down analog because the thiamin molecule cannot be simplified without losing biological activity.
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