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Altogether we have demonstrated our access to a range of very sequence-similar CBMs with diverse binding properties that can be used as a utility in analysis of the carbohydrate composition in lignocellulose materials.
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Chip-integrated arrays of silicon photonic microring resonators are refractive index sensitive devices that have optical properties that can be monitored to reveal the binding of biomolecules to target-specific capture agents.
There are 1,114 pairs with partial coverage properties that can be regarded as a subsequence of other binding sites.
We selected proteins in which removal/protection of the binding site is more specific, and determined whether these two classes of proteins differ by properties that can be described using Gene Ontology (GO) [ 28] terms.
As stated above, metal binding must alter the electronic and/or molecular structure of the sensor to induce changes in fluorescence properties that can be detected by a fluorescence microscope.
Among the various HU-nucleic acid binding properties that have been described, different DNA binding modes can be invoked to explain mechanistically its regulatory function.
Thus these lineages may provide unique peptide binding properties that uniquely widen the spectrum of pathogen peptides that a species can present.
All three complexes contain metal-binding properties that are entirely consistent with complexes of TBC[4], which itself can be regarded as a versatile ligand for polymetallic cluster construction.
The findings, presented here, recognize tRNA binding properties of CENUs that can further help in rational designing of more specific and efficient RNA targeted chemotherapeutic agents.
The advantages of using synthetic CBMs -which is novel for this study- over native CBMs is related to their molecular properties such as stability and binding specificity that can be targeted by engineering.
Using the SH3 domain of hematopoietic cell kinase as a test case, we show that SH3 binding properties can be profoundly altered by modifications within a hexapeptide sequence in the RT-loop region that is not involved in recognition of currently known consensus SH3 target peptides.
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