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dc.contributor.authorMedina, Ana
dc.contributor.authorTriviño, Josep
dc.contributor.authorBorges, Rafael J
dc.contributor.authorMillán, Claudia
dc.contributor.authorUsón, Isabel
dc.contributor.authorSammito, Massimo D
dc.date.accessioned2020-04-06T00:40:22Z
dc.date.available2020-04-06T00:40:22Z
dc.date.issued2020-02-26
dc.identifier.citationActa crystallographica. Section D, Structural biology, volume 76, issue Pt 3, page 193-208
dc.identifier.otherPMC7057218
dc.identifier.other32133985
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/304109
dc.description.abstractThe analysis of large structural databases reveals general features and relationships among proteins, providing useful insight. A different approach is required to characterize ubiquitous secondary-structure elements, where flexibility is essential in order to capture small local differences. The ALEPH software is optimized for the analysis and the extraction of small protein folds by relying on their geometry rather than on their sequence. The annotation of the structural variability of a given fold provides valuable information for fragment-based molecular-replacement methods, in which testing alternative model hypotheses can succeed in solving difficult structures when no homology models are available or are successful. ARCIMBOLDO_BORGES combines the use of composite secondary-structure elements as a search model with density modification and tracing to reveal the rest of the structure when both steps are successful. This phasing method relies on general fold libraries describing variations around a given pattern of β-sheets and helices extracted using ALEPH. The program introduces characteristic vectors defined from the main-chain atoms as a way to describe the geometrical properties of the structure. ALEPH encodes structural properties in a graph network, the exploration of which allows secondary-structure annotation, decomposition of a structure into small compact folds, generation of libraries of models representing a variation of a given fold and finally superposition of these folds onto a target structure. These functions are available through a graphical interface designed to interactively show the results of structure manipulation, annotation, fold decomposition, clustering and library generation. ALEPH can produce pictures of the graphs, structures and folds for publication purposes.
dc.languageeng
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceessn: 2059-7983
dc.sourcenlmid: 101676043
dc.subjectFolding
dc.subjectBioinformatics
dc.subjectCharacteristic Vector
dc.subjectAleph
dc.subjectFragment-based Libraries
dc.subjectX-ray Phasing
dc.subjectFold Clustering
dc.titleALEPH: a network-oriented approach for the generation of fragment-based libraries and for structure interpretation.
dc.typeArticle
dc.date.updated2020-04-06T00:40:21Z
dc.identifier.doi10.17863/CAM.51193
rioxxterms.versionofrecord10.1107/S2059798320001679
rioxxterms.versionVoR
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0/
dc.contributor.orcidMedina, Ana [0000-0001-7146-8987]
pubs.funder-project-idMinisterio de Economía, Industria y Competitividad, Gobierno de España (BIO2013-49604-EXP, BES-2017-080368, BES-2015-071397, MDM2014-0435-01, BIO2015-64216-P)
pubs.funder-project-idH2020 Marie Skłodowska-Curie Actions (790122)
pubs.funder-project-idFundação de Amparo à Pesquisa do Estado de São Paulo (17/13485-3, 16/24191-8)


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Attribution 4.0 International
Except where otherwise noted, this item's licence is described as Attribution 4.0 International