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dc.contributor.authorKursula, Petrien_US
dc.date.accessioned2020-06-17T17:34:27Z
dc.date.available2020-06-17T17:34:27Z
dc.date.issued2019-03-06
dc.PublishedKursula P. Shanks - multidomain molecular scaffolds of the postsynaptic density. Current Opinion in Structural Biology. 2019;54:122-128eng
dc.identifier.issn0959-440X
dc.identifier.issn1879-033X
dc.identifier.urihttps://hdl.handle.net/1956/22695
dc.description.abstractThe postsynaptic density (PSD) is a protein-rich assembly below the postsynaptic membrane, formed of large scaffolding proteins. These proteins carry a combination of protein interaction domains, which may interact with several alternative partners; the structure of the protein assembly can be regulated in an activity-dependent manner. A major scaffolding molecule in the PSD is Shank, a family of three main isoforms with highly similar domain structure. Proteins of the Shank family are targets of mutations in neurological disorders, such as autism and schizophrenia. All the predicted folded domains of Shank have now been crystallized. However, for an understanding of the structure and function of full-length Shank and its complexes in the supramolecular PSD assembly, novel complementary approaches and hybrid techniques must be employed.en_US
dc.language.isoengeng
dc.publisherElseviereng
dc.rightsAttribution CC BYeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.titleShanks - multidomain molecular scaffolds of the postsynaptic densityen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2020-01-29T08:46:18Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2019 The Author
dc.identifier.doihttps://doi.org/10.1016/j.sbi.2019.01.007
dc.identifier.cristin1702934
dc.source.journalCurrent Opinion in Structural Biology


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