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dc.contributor.authorMoynie, Lucile
dc.contributor.authorSchnell, Robert
dc.contributor.authorMcMahon, Stephen A.
dc.contributor.authorSandalova, Tatyana
dc.contributor.authorAbdelli Boulkeroua, Wassila
dc.contributor.authorSchmidberger, Jason W.
dc.contributor.authorAlphey, Magnus
dc.contributor.authorCukier, Cyprian
dc.contributor.authorDuthie, Fraser
dc.contributor.authorKopec, Jolanta
dc.contributor.authorLiu, Huanting
dc.contributor.authorJacewicz, Agata
dc.contributor.authorHunter, William N.
dc.contributor.authorNaismith, James H.
dc.contributor.authorSchneider, Gunter
dc.date.accessioned2013-02-11T16:31:02Z
dc.date.available2013-02-11T16:31:02Z
dc.date.issued2013-01
dc.identifier45303597
dc.identifierf75c15da-645a-42ed-9593-99a5b99ef68d
dc.identifier000313055000007
dc.identifier84872110709
dc.identifier.citationMoynie , L , Schnell , R , McMahon , S A , Sandalova , T , Abdelli Boulkeroua , W , Schmidberger , J W , Alphey , M , Cukier , C , Duthie , F , Kopec , J , Liu , H , Jacewicz , A , Hunter , W N , Naismith , J H & Schneider , G 2013 , ' The AEROPATH project targeting Pseudomonas aeruginosa : crystallographic studies for assessment of potential targets in early-stage drug discovery ' , Acta Crystallographica. Section F, Structural biology and crystallization communications , vol. 69 , no. 1 , pp. 25-34 . https://doi.org/10.1107/S1744309112044739en
dc.identifier.issn1744-3091
dc.identifier.otherORCID: /0000-0002-9353-3716/work/74510012
dc.identifier.urihttps://hdl.handle.net/10023/3352
dc.description.abstractBacterial infections are increasingly difficult to treat owing to the spread of antibiotic resistance. A major concern is Gram-negative bacteria, for which the discovery of new antimicrobial drugs has been particularly scarce. In an effort to accelerate early steps in drug discovery, the EU-funded AEROPATH project aims to identify novel targets in the opportunistic pathogen Pseudomonas aeruginosa by applying a multidisciplinary approach encompassing target validation, structural characterization, assay development and hit identification from small-molecule libraries. Here, the strategies used for target selection are described and progress in protein production and structure analysis is reported. Of the 102 selected targets, 84 could be produced in soluble form and the de novo structures of 39 proteins have been determined. The crystal structures of eight of these targets, ranging from hypothetical unknown proteins to metabolic enzymes from different functional classes (PA1645, PA1648, PA2169, PA3770, PA4098, PA4485, PA4992 and PA5259), are reported here. The structural information is expected to provide a firm basis for the improvement of hit compounds identified from fragment-based and high-throughput screening campaigns.
dc.format.extent10
dc.format.extent1660555
dc.language.isoeng
dc.relation.ispartofActa Crystallographica. Section F, Structural biology and crystallization communicationsen
dc.subjectAciden
dc.subjectReductaseen
dc.subjectMacromolecular crystallographyen
dc.subjectMolecular replacementen
dc.subjectSystemen
dc.subjectVI secretionen
dc.subjectDiffraction dataen
dc.subjectMechanistic implicationsen
dc.subjectCrystal-structureen
dc.subjectUroporphyrinogen-III synthaseen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleThe AEROPATH project targeting Pseudomonas aeruginosa : crystallographic studies for assessment of potential targets in early-stage drug discoveryen
dc.typeJournal articleen
dc.contributor.sponsorEuropean Commissionen
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.1107/S1744309112044739
dc.description.statusPeer revieweden
dc.identifier.grantnumberHEALTH-F3-2008-223461en


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