ALEPH: A Network-oriented approach for the generation of fragment-based libraries and for structure interpretation
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1107/S2059798320001679 http://hdl.handle.net/11449/198597 |
Resumo: | The 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. |
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Repositório Institucional da UNESP |
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spelling |
ALEPH: A Network-oriented approach for the generation of fragment-based libraries and for structure interpretationALEPHbioinformaticscharacteristic vectorfold clusteringfoldingfragment-based librariesX-ray phasingThe 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.Crystallographic Methods Institute of Molecular Biology of Barcelona (IBMB-CSIC) Barcelona Science Park, Helix Building, Baldiri Reixac 15Departamento de Física e Biofísica Instituto de Biociências Universidade Estadual Paulista (UNESP)Icrea Institució Catalana de Recerca i Estudis Avançats, Passeig Lluís Companys 23Department of Haematology Cambridge Institute for Medical Research University of Cambridge, Hills RoadDepartamento de Física e Biofísica Instituto de Biociências Universidade Estadual Paulista (UNESP)Barcelona Science ParkUniversidade Estadual Paulista (Unesp)Institució Catalana de Recerca i Estudis AvançatsUniversity of CambridgeMedina, AnaTriviño, JosepBorges, Rafael J. [UNESP]Millán, ClaudiaUsón, IsabelSammito, Massimo D.2020-12-12T01:17:10Z2020-12-12T01:17:10Z2020-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article193-208http://dx.doi.org/10.1107/S2059798320001679Acta Crystallographica Section D: Structural Biology, v. 76, p. 193-208.2059-7983http://hdl.handle.net/11449/19859710.1107/S20597983200016792-s2.0-85081042742Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengActa Crystallographica Section D: Structural Biologyinfo:eu-repo/semantics/openAccess2021-10-22T17:19:43Zoai:repositorio.unesp.br:11449/198597Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:09:25.547702Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
ALEPH: A Network-oriented approach for the generation of fragment-based libraries and for structure interpretation |
title |
ALEPH: A Network-oriented approach for the generation of fragment-based libraries and for structure interpretation |
spellingShingle |
ALEPH: A Network-oriented approach for the generation of fragment-based libraries and for structure interpretation Medina, Ana ALEPH bioinformatics characteristic vector fold clustering folding fragment-based libraries X-ray phasing |
title_short |
ALEPH: A Network-oriented approach for the generation of fragment-based libraries and for structure interpretation |
title_full |
ALEPH: A Network-oriented approach for the generation of fragment-based libraries and for structure interpretation |
title_fullStr |
ALEPH: A Network-oriented approach for the generation of fragment-based libraries and for structure interpretation |
title_full_unstemmed |
ALEPH: A Network-oriented approach for the generation of fragment-based libraries and for structure interpretation |
title_sort |
ALEPH: A Network-oriented approach for the generation of fragment-based libraries and for structure interpretation |
author |
Medina, Ana |
author_facet |
Medina, Ana Triviño, Josep Borges, Rafael J. [UNESP] Millán, Claudia Usón, Isabel Sammito, Massimo D. |
author_role |
author |
author2 |
Triviño, Josep Borges, Rafael J. [UNESP] Millán, Claudia Usón, Isabel Sammito, Massimo D. |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Barcelona Science Park Universidade Estadual Paulista (Unesp) Institució Catalana de Recerca i Estudis Avançats University of Cambridge |
dc.contributor.author.fl_str_mv |
Medina, Ana Triviño, Josep Borges, Rafael J. [UNESP] Millán, Claudia Usón, Isabel Sammito, Massimo D. |
dc.subject.por.fl_str_mv |
ALEPH bioinformatics characteristic vector fold clustering folding fragment-based libraries X-ray phasing |
topic |
ALEPH bioinformatics characteristic vector fold clustering folding fragment-based libraries X-ray phasing |
description |
The 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. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-12-12T01:17:10Z 2020-12-12T01:17:10Z 2020-03-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1107/S2059798320001679 Acta Crystallographica Section D: Structural Biology, v. 76, p. 193-208. 2059-7983 http://hdl.handle.net/11449/198597 10.1107/S2059798320001679 2-s2.0-85081042742 |
url |
http://dx.doi.org/10.1107/S2059798320001679 http://hdl.handle.net/11449/198597 |
identifier_str_mv |
Acta Crystallographica Section D: Structural Biology, v. 76, p. 193-208. 2059-7983 10.1107/S2059798320001679 2-s2.0-85081042742 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Acta Crystallographica Section D: Structural Biology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
193-208 |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129026174222336 |