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・ Morpeth Town A.F.C.
・ Morpeth, New South Wales
・ Morpeth, Northumberland
・ Morpeth, Ontario
・ Morph
・ Morph (animation)
・ Morph target animation
・ Morph the Cat
・ Morphaeus
・ Morphallaxis
・ Morphan
・ Morphaneflus
・ Morphant
・ Morphea
・ Morphea (comics)
Morpheein
・ Morpheis
・ Morpheis clenchi
・ Morpheis cognata
・ Morpheis comisteon
・ Morpheis discreta
・ Morpheis impedita
・ Morpheis lelex
・ Morpheis mathani
・ Morpheis melanoleuca
・ Morpheis pyracmon
・ Morpheis strigillata
・ Morpheis votani
・ Morpheis xylotribus
・ Morphem (musician)


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Morpheein : ウィキペディア英語版
Morpheein

Morpheeins are proteins that can form two or more different homo-oligomers (morpheein forms), but must come apart and change shape to convert between forms. The alternate shape may reassemble to a different oligomer. The shape of the subunit dictates which oligomer is formed. Each oligomer has a finite number of subunits (stoichiometry). Morpheeins can interconvert between forms under physiological conditions and can exist as an equilibrium of different oligomers. These oligomers are physiologically relevant and are not misfolded protein; this distinguishes morpheeins from prions and amyloid. The different oligomers have distinct functionality. Interconversion of morpheein forms can be a structural basis for allosteric regulation.〔〔 A mutation that shifts the normal equilibrium of morpheein forms can serve as the basis for a conformational disease. Features of morpheeins can be exploited for drug discovery.〔〔Lawrence Ramirez (2008).〕 The dice image (Fig 1) represents a morpheein equilibrium containing two different monomeric shapes that dictate assembly to a tetramer or a pentamer. The one protein that is established to function as a morpheein is porphobilinogen synthase,〔 though there are suggestions throughout the literature that other proteins may function as morpheeins (for more information see "Table of Putative Morpheeins" below).
== Implications for drug discovery ==

Conformational differences between subunits of different oligomers and related functional differences of a morpheein provide a starting point for drug discovery. Protein function is dependent on the oligomeric form; therefore, the protein’s function can be regulated by shifting the equilibrium of forms. A small molecule compound can shift the equilibrium either by blocking or favoring formation of one of the oligomers. The equilibrium can be shifted using a small molecule that has a preferential binding affinity for only one of the alternate morpheein forms. An inhibitor of porphobilinogen synthase with this mechanism of action has been documented.〔


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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