conformational's Usage Examples:

In chemistry, conformational isomerism is a form of stereoisomerism in which the isomers can be interconverted just by rotations about formally single.

In biochemistry, a conformational change is a change in the shape of a macromolecule, often induced by environmental factors.

the induced fit model, and the conformational selection model.

The latter two are not mutually exclusive: conformational selection can be followed by a.

sites allow effectors to bind to the protein, often resulting in a conformational change involving protein dynamics.

two categories, conformational epitopes and linear epitopes, based on their structure and interaction with the paratope.

chemical bond connecting two sp3-hybridised atoms, and is normally a conformational energy minimum.

Polymorphism in organic compounds is often the result of conformational polymorphism.

The classical structural GDP/GTP switch is characterised by conformational changes at the so-called switch 1 and switch 2 regions, which bind tightly.

as different conformations, and transitions between them are called conformational changes.

Light leads to conformational changes in rhodopsin, which in turn leads to the activation of transducin.

A conformational epitope is a sequence of sub-units (usually amino acids) composing an antigen that come in direct contact with a receptor of the immune.

channels by physically blocking the channel-entrance and inducing a conformational change in the K+-selectivity filter of the channel.

unique conformational change also makes them of interest to the structural biology and protein folding research communities.

The conformational-change.

When the 50S subunit joins, it hydrolyzes GTP to GDP and Pi, causing a conformational change in the IF2 that causes IF2 to release and allow the 70S ribosome.

femtochemistry in biological studies has also helped to elucidate the conformational dynamics of stem-loop RNA structures.

This causes a conformational change in the large loop which then creates sites for oligosaccharide.

that are the same stereoisomer as each other might be in different conformational forms or be different isotopologues.