Sentence examples for bridge anchoring from inspiring English sources

The predicted salt bridge anchoring the anionic 5′-carboxylate to the side chain of Lys178 was observed in the crystal structure.

FEM 3D models of the bridge and of the bridge anchored to the bone by implants have been developed.

The macro model represents the non-linear soil structure interaction (SSI) exemplified by a suspension bridge anchor-block.

This computational study gave reliable structural models for D2, 5-HT2A, and 5-HT7, whadh had overall structural complementarities with a salt bridge anchor at the center of the lurasidone molecule, but not for H1 and M1 owing to steric hindrance between the norbornane-2,3-dicarboximide and/or cyclohexane part of lurasidone and both receptors.

The following findings are recorded: extracted teeth due to caries, not replaced; missing, non-replaced teeth, missing for reasons other than caries; full crown; partial crown (at least one cusp covered); anchor crown (bridge anchor, telescopic crown, crown anchored to bar, root caps); pontic (fixed prosthesis); replaced tooth (removable prosthesis); implant (with prosthetic restoration).

In the third experiment, Mg2+ titrations were carried out to determine whether mutation of a bridge-anchoring residue alters the affinity of the coordinating metal ion.

Therefore, to address this issue, the interactions of ciprofloxacin and related drugs (quinazolinediones) with wild-type E. coli topoisomerase IV and a series of enzymes with mutations in the predicted bridge-anchoring residues (ParC Ser80 and Glu84) were analyzed.

As a first step toward determining whether the water metal ion bridge is a general mechanism of quinolone topoisomerase interaction, we characterized drug interactions with wild-type Escherichia coli (Gram-negative) topoisomerase IV and a series of ParC enzymes with mutations (S80L, S80I, S80F, and E84K) in the predicted bridge-anchoring residues.

Two chiral manganese(III) salen catalysts, bearing different chiral diamine bridges, were anchored by direct axial coordination of the metal centre onto the phenolate groups of a modified commercial activated carbon.

Due to their high reactivity the opened bridges can anchor a gold plate more efficiently than other sites of the macromolecule giving rise to preferential orientations of the variable part of the antibody.

Docking study of the most active compounds against 5-HT7R and 5-HT1AR revealed that both receptors have two hydrophobic pockets around the anchoring salt bridge.