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dc.contributor.authorLoizidou, Eriketi Z.en
dc.contributor.authorZeinalipour-Yazdi, Constantinos D.en
dc.creatorLoizidou, Eriketi Z.en
dc.creatorZeinalipour-Yazdi, Constantinos D.en
dc.date.accessioned2019-11-21T06:21:13Z
dc.date.available2019-11-21T06:21:13Z
dc.date.issued2014
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55800
dc.source.urihttps://nls.ldls.org.uk/welcome.html?ark:/81055/vdc_100024867322.0x000036
dc.subjectDrugsen
dc.subjectDesignen
dc.subjectBiochemistryen
dc.subjectPharmaceutical chemistryen
dc.titleComputational Inhibition Studies of the Human Proteasome by Argyrin‐Based Analogues with Subunit Specificityen
dc.typeinfo:eu-repo/semantics/article
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.description.notes<p>ID: 770en
dc.description.notesIn: Chemical biology & drug design, Vol. 84, no. 1 (July 2014), p.99-107.en
dc.description.notesSummary: Abstract A computational procedure was developed to study the subunit‐specific interactions of the proteasome inhibitors argyrin A and F, with the aim of indentifying the determinants of subunit selectivity. Three‐dimensional models of humanized proteasome active sites β1, β2 and β5 were developed and subsequently used in molecular docking simulations with the argyrin analogues. The subunit selectivity exhibited by each analogue could be explained based on the site‐specific interactions and a probability‐based specificity parameter derived in this study. A rational approach that involved maximizing site‐specific interactions was followed to guide the design of new argyrin analogues as specific inhibitors of the caspase‐like (β1 site) activity.</p>en
dc.contributor.orcidZeinalipour-Yazdi, Constantinos D. [0000-0002-8388-1549]
dc.gnosis.orcid0000-0002-8388-1549


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