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Protein-based pharmacophores refer to the potential interaction sites for the ligand to favorably interact with the protein atoms in the binding site.
These results imply that NaSCN and urea favorably interact with the aromatic sidewalls of SWCNTs.
InhA enzyme was chosen based upon its hydrophobic properties that favorably interact with thioamide or thiourea moieties [25].
The polar ClMS groups provide anchoring sites with the polar SiOx/Si substrate while the styrene segments favorably interact with the PS matrix.
Unstructured regions have a large solvent-accessible area, which explains why polar and charged residues, which favorably interact with water, are prevalent in these regions.
Orange G, as well as screened BAFs, favorably interact with the in-register fiber and are compatible with the geometry of the Lys residues aligned in in-register β-sheets.
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InhA enzyme was chosen as it contains a very hydrophobic site that favorably interacts with thioamide or thiourea moieties [25].
Nonetheless, according to the inhibitor-bound BoNTAe complexes generated by MMDSs, we conjectured that the benzyl group of 10b could interact favorably with the serotype-specific Phe194 via the pi-pi interaction.
Aromatic amino acids interact favorably with proline residues via both the hydrophobic effect and aromatic proline interactions, C−H/π interactions between the aromatic π face and proline ring C H bonds.
Cycling alters the selectivity by creating waves of concentrations within the catalyst which interact favorably in this instance.
In addition, SANS measurements also indicate that the DN-gel constituents interact favorably with each other while in water.
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