pE-DB: a database of structural ensembles of intrinsically disordered and of unfolded proteins

dc.contributor.authorVaradi, Mihaly
dc.contributor.authorKosol, Simone
dc.contributor.authorLebrun, Pierre
dc.contributor.authorValentini, Erica
dc.contributor.authorBlackledge, Martin
dc.contributor.authorDunker, A. Keith
dc.contributor.authorFelli, Isabella C.
dc.contributor.authorForman-Kay, Julie D.
dc.contributor.authorKriwacki, Richard W.
dc.contributor.authorPierattelli, Roberta
dc.contributor.authorSussman, Joel
dc.contributor.authorSvergun, Dmitri I.
dc.contributor.authorUversky, Vladimir N.
dc.contributor.authorVendruscolo, Michele
dc.contributor.authorWishart, David
dc.contributor.authorWright, Peter E.
dc.contributor.authorTompa, Peter
dc.contributor.departmentBiochemistry and Molecular Biology, School of Medicine
dc.date.accessioned2025-04-28T15:26:47Z
dc.date.available2025-04-28T15:26:47Z
dc.date.issued2014
dc.description.abstractThe goal of pE-DB (http://pedb.vib.be) is to serve as an openly accessible database for the deposition of structural ensembles of intrinsically disordered proteins (IDPs) and of denatured proteins based on nuclear magnetic resonance spectroscopy, small-angle X-ray scattering and other data measured in solution. Owing to the inherent flexibility of IDPs, solution techniques are particularly appropriate for characterizing their biophysical properties, and structural ensembles in agreement with these data provide a convenient tool for describing the underlying conformational sampling. Database entries consist of (i) primary experimental data with descriptions of the acquisition methods and algorithms used for the ensemble calculations, and (ii) the structural ensembles consistent with these data, provided as a set of models in a Protein Data Bank format. PE-DB is open for submissions from the community, and is intended as a forum for disseminating the structural ensembles and the methodologies used to generate them. While the need to represent the IDP structures is clear, methods for determining and evaluating the structural ensembles are still evolving. The availability of the pE-DB database is expected to promote the development of new modeling methods and leads to a better understanding of how function arises from disordered states.
dc.eprint.versionFinal published version
dc.identifier.citationVaradi M, Kosol S, Lebrun P, et al. pE-DB: a database of structural ensembles of intrinsically disordered and of unfolded proteins. Nucleic Acids Res. 2014;42(Database issue):D326-D335. doi:10.1093/nar/gkt960
dc.identifier.urihttps://hdl.handle.net/1805/47516
dc.language.isoen_US
dc.publisherOxford University Press
dc.relation.isversionof10.1093/nar/gkt960
dc.relation.journalNucleic Acids Research
dc.rightsAttribution-NonCommercial 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.sourcePMC
dc.subjectIntrinsically disordered proteins
dc.subjectProtein unfolding
dc.subjectX-ray diffraction
dc.titlepE-DB: a database of structural ensembles of intrinsically disordered and of unfolded proteins
dc.typeArticle
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Varadi2013Database-CCBYNC.pdf
Size:
8.87 MB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
2.04 KB
Format:
Item-specific license agreed upon to submission
Description: