Enzyme Tunnels and Gates As Relevant Targets in Drug Design

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Publikace nespadá pod Filozofickou fakultu, ale pod Přírodovědeckou fakultu. Oficiální stránka publikace je na webu muni.cz.

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MARQUES Sérgio Manuel DANIEL Lukáš BURYŠKA Tomáš PROKOP Zbyněk BREZOVSKÝ Jan DAMBORSKÝ Jiří

Rok publikování 2017
Druh Článek v odborném periodiku
Časopis / Zdroj MEDICINAL RESEARCH REVIEWS
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www https://loschmidt.chemi.muni.cz/peg/wp-content/uploads/2016/12/Marques_16res_rev.pdf
Doi http://dx.doi.org/10.1002/med.21430
Klíčová slova drug design; protein tunnels; protein gates; drug binding; selectivity; specificity
Popis Many enzymes contain tunnels and gates that are essential to their function. Gates reversibly switch between open and closed conformations and thereby control the traffic of small molecules-substrates, products, ions, and solvent molecules-into and out of the enzyme's structure via molecular tunnels. Many transient tunnels and gates undoubtedly remain to be identified, and their functional roles and utility as potential drug targets have received comparatively little attention. Here, we describe a set of general concepts relating to the structural properties, function, and classification of these interesting structural features. In addition, we highlight the potential of enzyme tunnels and gates as targets for the binding of small molecules. The different types of binding that are possible and the potential pharmacological benefits of such targeting are discussed. Twelve examples of ligands bound to the tunnels and/or gates of clinically relevant enzymes are used to illustrate the different binding modes and to explain some new strategies for drug design. Such strategies could potentially help to overcome some of the problems facing medicinal chemists and lead to the discovery of more effective drugs.
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