Sentence examples for structurally bound from inspiring English sources

Exact(28)

The model of rhodopsin in Figure 20 also reflects results from GPCR sequence analyses, with the ribbon thickness coding for amino acid conservation, and results from GPCR structure analyses, where structurally bound waters are observed in "homologous" positions.

> -wrap-foot> aDetection limits (KOH-soluble F = 0.544 μg/cm, structurally bound fluoride = 604.8 μg/cm) In Table  3, KOH-soluble fluoride and structurally bound fluoride data of the experimental groups are given, for which more than 50% of the readings were above detection limit.

In general, devolatilization reactions are temperature-sensitive, reflecting the large increase in entropy (disorder) that accompanies release of structurally bound hydroxyl groups (OH) from minerals to produce molecular water.

This Raman intensity includes contributions from both molecular H2O and structurally bound OH groups.

Water is dissolved in silicate melts in the form of water molecules, H2O0, and structurally bound hydroxyl groups, OH.

Since the REE may be structurally bound within the clays (as opposed to sorbed at surface sites) [32], it is possible that produced water REE profiles will not resemble those of the bulk shale.

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Similar(32)

This temperature was kept constant for 20 min to ensure that any free water (i.e. non-structurally bound) was removed.

Based on superimpositions of the SULT1E1 structures bound to TBBPA, 3-OH-BDE-47, 4,4´- OH 2-3,5,3´,5´-tetrachlorobiphenyl, and E2, it appears that SULT1E1 is able to bind these structurally diverse compounds with only minor changes in a few sidechain residues and small shifts in loop 84,4´- OH 2-3,5,3´,5´-tetrachlorobiphenyl S5 and S6).

Its central hypothesis is that structurally similar binding sites bind structurally similar ligands.

The alignment of the molecules was based on the conformation of a structurally related ligand bound to the αIIBβ3 and αvβ3 integrins in X-ray crystallographic studies.

However, the weak point of this method is that it cannot consider many structurally unrelated drugs bound to a common target [ 18, 19].

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