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http://purl.uniprot.org/citations/28154144http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28154144http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28154144http://www.w3.org/2000/01/rdf-schema#comment"The exact function of human gasdermin-B (GSDMB), which regulates differentiation and growth of epithelial cells, is yet to be elucidated. In human epidermal growth factor receptor 2 (HER2)-positive breast cancer, GSDMB gene amplification and protein overexpression indicate a poor response to HER2-targeted therapy. Genome-wide association studies revealed a correlation between GSDMB SNPs and an increased susceptibility to Crohn's disease, ulcerative colitis, and asthma. The N- and C-terminal domains of all gasdermins possess lipid-binding and regulatory activities, respectively. Inflammatory caspases cleave gasdermin-D in the interdomain linker but not GSDMB. The cleaved N-terminal domain binds phosphoinositides and cardiolipin, forms membrane-disrupting pores, and executes pyroptosis. We show that both full-length GSDMB and the N-terminal domain bind to nitrocellulose membranes immobilized with phosphoinositides or sulfatide, but not with cardiolipin. In addition, the GSDMB N-terminal domain binds liposomes containing sulfatide. The crystal structure of the GSDMB C-terminal domain reveals the structural impact of the amino acids encoded by SNPs that are linked to asthma and inflammatory bowel disease (IBD). A loop that carries the polymorphism amino acids corresponding to healthy individuals (Gly299:Pro306) exhibits high conformational flexibility, whereas the loop carrying amino acids found in individuals with increased disease risk (Arg299:Ser306) exhibits a well-defined conformation and higher positive surface charge. Apoptotic executioner caspase-3, -6, and -7, but not the inflammatory caspases, cleave GSDMB at 88DNVD91 within the N-terminal domain. Selective sulfatide binding may indicate possible function for GSDMB in the cellular sulfatide transport."xsd:string
http://purl.uniprot.org/citations/28154144http://purl.org/dc/terms/identifier"doi:10.1073/pnas.1616783114"xsd:string
http://purl.uniprot.org/citations/28154144http://purl.org/dc/terms/identifier"doi:10.1073/pnas.1616783114"xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/author"Herzberg O."xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/author"Herzberg O."xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/author"Kulakova L."xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/author"Kulakova L."xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/author"Chao K.L."xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/author"Chao K.L."xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/name"Proc. Natl. Acad. Sci. U.S.A."xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/name"Proc. Natl. Acad. Sci. U.S.A."xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/pages"E1128-E1137"xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/pages"E1128-E1137"xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/title"Gene polymorphism linked to increased asthma and IBD risk alters gasdermin-B structure, a sulfatide and phosphoinositide binding protein."xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/title"Gene polymorphism linked to increased asthma and IBD risk alters gasdermin-B structure, a sulfatide and phosphoinositide binding protein."xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/volume"114"xsd:string
http://purl.uniprot.org/citations/28154144http://purl.uniprot.org/core/volume"114"xsd:string
http://purl.uniprot.org/citations/28154144http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/28154144
http://purl.uniprot.org/citations/28154144http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/28154144
http://purl.uniprot.org/citations/28154144http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/28154144
http://purl.uniprot.org/citations/28154144http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/28154144