Sentence examples for acidic side from inspiring English sources

The phrase "acidic side" is correct and usable in written English.
It can be used in contexts related to chemistry, biology, or discussions about flavors and pH levels.
Example: "The acidic side of the solution was measured to determine its potential reactivity with other substances."
Alternatives: "sour aspect" or "low pH side".

Exact(58)

This is, however, a very conservative substitution, as both aspartic acid and glutamic acid have acidic side chains, and thus would probably not significantly disrupt calcium binding.

AtAAP6 was reported to be expressed in sink tissue with a high affinity for neutral amino acids and other amino acids with acidic side chains (Hunt et al. 2010).

DAAO has weak activity towards D-amino acids with acidic side chains, but has significant activity to oxidize a diversity of D-amino acids, typically amino acids with small hydrophilic, large aromatic or basic side chains [ 1, 2].

Charges on the residue X prevent the self-assembly, and by choosing amino acids with basic or acidic side chains, self-assembly of the protein filaments can be controlled by pH.

To the above bands, infrared absorptions of hydrocarbon groups, as well as those of functional side groups of amino acids such as glutamic and aspartic acid, may be added; absorptions of acidic side chains depend heavily on the current pH of the material [44].

Possibly, acidic side chains such as glucopyranosyluronic acid formed during the xylan degradation, causing the precipitation in the low pH environment [ 44].

While the hydrophobic character at W626, L625 and W463 is again conserved, the central methionine is replaced by a glutamic acid, making it highly unlikely the two acidic side chains could pack closely together.

The terminal amino acid for MV is D (i.e., YNDRNLLD) while that of CDV is N (i.e., YSDKELLN), making the total content of acidic side groups in the terminal 8 amino acids comparable.

The gas-phase basicity values in Table 2 indicate that negative-charge locations in gaseous, multiply deprotonated peptides and proteins are by preference at acidic side chains, that is, glutamic and aspartic acid residues and the C terminus.

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Similar(2)

SMU.440 also shares a similar binding pocket composed primarily of residues with aromatic and acidic side-chains, which points to a potential binding of a polyketide-like molecule.

Although the bn2 aspartate 296 mutation is in a position opposite the native catalytic aspartates, it is oriented such that the acidic side-chain is immediately adjacent to the valyl-adenylate substrate.

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