The molecular basis for the selection of captopril cis and trans conformations by angiotensin I converting enzyme

dc.contributor.authorTzakos, A. G.en
dc.contributor.authorNaqvi, N.en
dc.contributor.authorComporozos, K.en
dc.contributor.authorPierattelli, R.en
dc.contributor.authorTheodorou, V.en
dc.contributor.authorHusain, A.en
dc.contributor.authorGerothanassis, I. P.en
dc.date.accessioned2015-11-24T16:50:56Z
dc.date.available2015-11-24T16:50:56Z
dc.identifier.issn0960-894X-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9661
dc.rightsDefault Licence-
dc.subjectangiotensin-converting enzymeen
dc.subjectcaptoprilen
dc.subjectisomerizationen
dc.subjectmutagenesisen
dc.subjectnmren
dc.subjectcrystal-structureen
dc.subjectdomainen
dc.subjectlisinoprilen
dc.subjectinhibitorsen
dc.subjectbindingen
dc.titleThe molecular basis for the selection of captopril cis and trans conformations by angiotensin I converting enzymeen
heal.abstractEnzyme-inhibitor recognition is considered one of the most fundamental aspects in the area of drug discovery. However, the molecular mechanism of this recognition process (induced fit or prebinding and adaptive selection among multiple conformers) in several cases remains unexplored. In order to shed light toward this step of the recognition process in the case of human angiotensin I converting enzyme (hACE) and its inhibitor captopril, we have established a novel combinatorial approach exploiting solution NMR, flexible docking calculations, mutagenesis, and enzymatic studies. We provide evidence that an equimolar ratio of the cis and trans states of captopril exists in solution and that the enzyme selects only the trans state of the inhibitor that presents architectural and stereoelectronic complementarity with its substrate binding groove. (c) 2006 Elsevier Ltd. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.bmcl.2006.07.034-
heal.identifier.secondary<Go to ISI>://000240615400020-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0960894X06008092/1-s2.0-S0960894X06008092-main.pdf?_tid=a916c5e4-3a30-11e3-be14-00000aacb35f&acdnat=1382346822_2b15eb78a7a161b542c37de9619819c8-
heal.journalNameBioorganic and Medicinal Chemistry Lettersen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2006-
heal.publisherElsevieren
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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