Sentence examples for modify the side from inspiring English sources

We consider a DISCOVER DVC system and modify the side information generation and fusion steps, using the methods proposed in the previous sections.

In particular, selective functionalization of either the primary or secondary C sp3)H bonds in the amino acids has been explored to make versatile CC, CN, CO, CB and CF bonds to modify the side chain of amino acids and even peptides.

Methylthioalkylmalate synthases encoded at the MAM locus determine the side chain length of the methionine-derived precursors, while 2-oxoglutarate-dependent dioxygenases encoded at AOP modify the side chain structure.

Therefore, co-expressing the GH115 α-glucuronidase with an acetyl xylan esterase can be a strategic approach to modify the side groups of cell wall xylans.

The lignin specific pathway then uses p-coumaroyl-CoA to produce the simplest monolignol, H monolignol (p-coumaryl alcohol), through a series of reduction reactions that modify the side chain [ 7].

Administering chemotherapy weekly to modify the side-effect profile without decreasing efficacy is a well-established policy in other solid malignancies.

Additionally, it is easy to change their properties by modifying the side chains.

In this study, we modified the side chains of maleate diesters to be linear (i.e., unbranched) alkyl chains that varied in length from ethyl to n-octyl.

Using the crystal structure of H5N1 NA (PDB ID: 2hty) as the starting point, in a set of 54 inhibitors previously proposed by modifying the side chains of oseltamivir, 4 inhibitors were identified using two different computational strategies (ArgusLab4.0.1, FlexX-E3.0.1) both to lower the binding free energy (BFE) of oseltamivir and to have partially acceptable conformations.

This enzyme modifies the side chains of serine and threonine residues of nuclear and cytosolic proteins with GlcNAc [21] [24].

While for the reason that the structure of the side chain is critical for the specificity of antiviral action, only modifying the side chain as phosphate ester or amide linker is favorable to improve the oral bioavailability.