Sentence examples for accommodate the charge from inspiring English sources

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Interesting is the change in protonation of this ligand to accommodate the charge balance, well demonstrating its flexibility, and also the change in bonding mode; although in the iron compound this is less protonated and the bonding is less extensive.

We note the molecular formula used to calculate the theoretical mass of modified ToyJ is that of the neutral molecule wherein three protons have been removed to accommodate the charge of the trivalent cobalt atom.

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Race organizers scrambled for a solution to accommodate the charging peloton, telling teams that the finish would take place at the banner a little less than two miles from the original line.

A change in the configuration of the H-bond donors and acceptors could accommodate the charged and uncharged forms of the uracil ring, maintaining a similar network.

We therefore postulate that this internal cavity is the likely site for accommodating the charged phospholipid head group of PA.

The presence of the aromatic ring enforces the geometry of the product, and the reaction is favoured by electron-withdrawing groups, such as the nitro (−NO2) group, which help to accommodate the negative charge on the intermediate.

If we consider a public charging station, with the possibility to accommodate the parallel charging of several vehicles, this can be ideally seen as a grid-connected battery; the charging load due EV parallel charging can cope with high PV generation, by activation from a centralized position.

Additionally, catalytically active A3s share a positively charged groove near the Zn2+ coordinating active site, which may accommodate the negatively charged polynucleotide substrate.

The crystal structure of the yeast ortholog of DOT1L, Dot1p, highlights an acidic cleft that could accommodate the basic charges surrounding H3K79, including R72 and R83.

13 Our homology models predict that both A+A− and A+B− binding sites contain these residues, providing an aromatic environment to accommodate the positively charged moiety that is a well-known pharmacophore feature of 5-HT3 ligands.

Although definitive conclusions using a static structure are limited and lack any kinetic information about the binding site interactions, substituting the middle X residue into the structure provides a qualitative picture of the molecular gyrations needed to accommodate the differently charged and sized amino acid side chains.

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