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1.
Beilstein J Org Chem ; 20: 931-939, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38711584

RESUMO

The remediation of the carbohydrate data of the Protein Data Bank (PDB) has brought numerous enhancements to the findability and interpretability of deposited glycan structures, yet crucial quality indicators are either missing or hard to find on the PDB pages. Without a way to access wider glycochemical context, problematic structures may be taken as fact by keen but inexperienced scientists. The Privateer software is a validation and analysis tool that provides access to a number of metrics and links to external experimental resources, allowing users to evaluate structures using carbohydrate-specific methods. Here, we present the Privateer database, a free resource that aims to complement the growing glycan content of the PDB.

2.
Acta Crystallogr F Struct Biol Commun ; 80(Pt 2): 30-35, 2024 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-38265073

RESUMO

Owing to the difficulties associated with working with carbohydrates, validating glycan 3D structures prior to deposition into the Protein Data Bank has become a staple of the structure-solution pipeline. The Privateer software provides integrative methods for the validation, analysis, refinement and graphical representation of 3D atomic structures of glycans, both as ligands and as protein modifiers. While Privateer is free software, it requires users to install any of the structural biology software suites that support it or to build it from source code. Here, the Privateer web app is presented, which is always up to date and available to be used online (https://privateer.york.ac.uk) without installation. This self-updating tool, which runs locally on the user's machine, will allow structural biologists to simply and quickly analyse carbohydrate ligands and protein glycosylation from a web browser whilst retaining all confidential information on their devices.


Assuntos
Carboidratos , Aplicativos Móveis , Carboidratos/química , Cristalografia por Raios X , Glicosilação , Polissacarídeos/química
3.
Acta Crystallogr D Struct Biol ; 79(Pt 6): 449-461, 2023 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-37259835

RESUMO

The Collaborative Computational Project No. 4 (CCP4) is a UK-led international collective with a mission to develop, test, distribute and promote software for macromolecular crystallography. The CCP4 suite is a multiplatform collection of programs brought together by familiar execution routines, a set of common libraries and graphical interfaces. The CCP4 suite has experienced several considerable changes since its last reference article, involving new infrastructure, original programs and graphical interfaces. This article, which is intended as a general literature citation for the use of the CCP4 software suite in structure determination, will guide the reader through such transformations, offering a general overview of the new features and outlining future developments. As such, it aims to highlight the individual programs that comprise the suite and to provide the latest references to them for perusal by crystallographers around the world.


Assuntos
Proteínas , Software , Proteínas/química , Cristalografia por Raios X , Substâncias Macromoleculares
4.
Acta Crystallogr D Struct Biol ; 79(Pt 6): 462-472, 2023 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-37219590

RESUMO

The oligosaccharides in N-glycosylation provide key structural and functional contributions to a glycoprotein. These contributions are dependent on the composition and overall conformation of the glycans. The Privateer software allows structural biologists to evaluate and improve the atomic structures of carbohydrates, including N-glycans; this software has recently been extended to check glycan composition through the use of glycomics data. Here, a broadening of the scope of the software to analyse and validate the overall conformation of N-glycans is presented, focusing on a newly compiled set of glycosidic linkage torsional preferences harvested from a curated set of glycoprotein models.


Assuntos
Oligossacarídeos , Polissacarídeos , Polissacarídeos/química , Oligossacarídeos/química , Glicoproteínas/química , Glicosilação , Glicômica , Configuração de Carboidratos
6.
Beilstein J Org Chem ; 16: 2523-2533, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-33093930

RESUMO

The heterogeneity, mobility and complexity of glycans in glycoproteins have been, and currently remain, significant challenges in structural biology. These aspects present unique problems to the two most prolific techniques: X-ray crystallography and cryo-electron microscopy. At the same time, advances in mass spectrometry have made it possible to get deeper insights on precisely the information that is most difficult to recover by structure solution methods: the full-length glycan composition, including linkage details for the glycosidic bonds. The developments have given rise to glycomics. Thankfully, several large scale glycomics initiatives have stored results in publicly available databases, some of which can be accessed through API interfaces. In the present work, we will describe how the Privateer carbohydrate structure validation software has been extended to harness results from glycomics projects, and its use to greatly improve the validation of 3D glycoprotein structures.

7.
Curr Opin Struct Biol ; 62: 70-78, 2020 06.
Artigo em Inglês | MEDLINE | ID: mdl-31874387

RESUMO

The methodology underpinning the construction, refinement, validation and analysis of atomic models of glycoproteins and protein-carbohydrate complexes has received a long-overdue boost in the last five years. This is a very timely development, as the resolution revolution in electron cryo-microscopy is now routinely delivering structures of key glycomedical importance, with a three-dimensional precision where X-ray crystallographic methods have traditionally floundered. This review will focus on the new software developments that have been introduced in the past two years, and their impact on the field of structural glycobiology in terms of published structures.


Assuntos
Microscopia Crioeletrônica/métodos , Glicômica/métodos , Glicoproteínas/química , Software , Modelos Moleculares , Estrutura Molecular
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