Conformational flexibility and molecular interactions of an archaeal homologue of the Shwachman-Bodian-Diamond syndrome protein

BACKGROUND: Defects in the human Shwachman-Bodian-Diamond syndrome (SBDS) protein-coding gene lead to the autosomal recessive disorder characterised by bone marrow dysfunction, exocrine pancreatic insufficiency and skeletal abnormalities. This protein is highly conserved in eukaryotes and archaea bu...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Ng, C Leong, Waterman, David G, Koonin, Eugene V, Walters, Alison D, Chong, James PJ, Isupov, Michail N, Lebedev, Andrey A, Bunka, David HJ, Stockley, Peter G, Ortiz-Lombardía, Miguel, Antson, Alfred A
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2009
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2695463/
https://ncbi.nlm.nih.gov/pubmed/19454024
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1472-6807-9-32
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