Structure of the N‐terminal domain of the protein Expansion: an `Expansion' to the Smad MH2 fold. (1st April 2015)
- Record Type:
- Journal Article
- Title:
- Structure of the N‐terminal domain of the protein Expansion: an `Expansion' to the Smad MH2 fold. (1st April 2015)
- Main Title:
- Structure of the N‐terminal domain of the protein Expansion: an `Expansion' to the Smad MH2 fold
- Authors:
- Beich‐Frandsen, Mads
Aragón, Eric
Llimargas, Marta
Benach, Jordi
Riera, Antoni
Pous, Joan
Macias, Maria J. - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Gene‐expression changes observed in <italic>Drosophila</italic> embryos after inducing the transcription factor Tramtrack led to the identification of the protein Expansion. Expansion contains an N‐terminal domain similar in sequence to the MH2 domain characteristic of Smad proteins, which are the central mediators of the effects of the TGF‐β signalling pathway. Apart from Smads and Expansion, no other type of protein belonging to the known kingdoms of life contains MH2 domains. To compare the Expansion and Smad MH2 domains, the crystal structure of the Expansion domain was determined at 1.6 Å resolution, the first structure of a non‐Smad MH2 domain to be characterized to date. The structure displays the main features of the canonical MH2 fold with two main differences: the addition of an α‐helical region and the remodelling of a protein‐interaction site that is conserved in the MH2 domain of Smads. Owing to these differences, to the new domain was referred to as Nα‐MH2. Despite the presence of the Nα‐MH2 domain, Expansion does not participate in TGF‐β signalling; instead, it is required for other activities specific to the protostome phyla. Based on the structural similarities to the MH2 fold, it is proposed that the Nα‐MH2 domain should be classified as a new member of the Smad/FHA superfamily.</p> </abstract>
- Is Part Of:
- Acta crystallographica. Volume 71:Part 4(2015:Apr.)
- Journal:
- Acta crystallographica
- Issue:
- Volume 71:Part 4(2015:Apr.)
- Issue Display:
- Volume 71, Issue 4, Part 4 (2015)
- Year:
- 2015
- Volume:
- 71
- Issue:
- 4
- Part:
- 4
- Issue Sort Value:
- 2015-0071-0004-0004
- Page Start:
- 844
- Page End:
- 853
- Publication Date:
- 2015-04-01
- Subjects:
- Biomolecules -- Structure -- Periodicals
Physical biochemistry -- Periodicals
X-ray crystallography -- Periodicals
Crystallography -- Periodicals
572 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://www.blackwell-synergy.com/loi/ayd ↗
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http://www.iucr.ac.uk/journals/acta/actad.html ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1107/S1399004715001443 ↗
- Languages:
- English
- ISSNs:
- 0907-4449
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0612.022000
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British Library STI - ELD Digital store - Ingest File:
- 3363.xml