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http://purl.uniprot.org/citations/22802649http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/22802649http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/22802649http://www.w3.org/2000/01/rdf-schema#comment"Interleukin 20 (IL-20) is a pleotropic IL-10 family cytokine that protects epithelial surfaces from pathogens. However, dysregulated IL-20 signaling is implicated in several human pathologies including psoriasis, rheumatoid arthritis, atherosclerosis, and osteoporosis. IL-20, and related cytokines IL-19 and IL-24, designated IL-20 subfamily cytokines (IL-20SFCs), induce cellular responses through an IL-20R1/IL-20R2 (type I) receptor heterodimer, whereas IL-20 and IL-24 also signal through the IL-22R1/IL-20R2 (type II) receptor complex. The crystal structure of the IL-20/IL-20R1/IL-20R2 complex reveals how type I and II complexes discriminate cognate from noncognate ligands. The structure also defines how the receptor-cytokine interfaces are affinity tuned to allow distinct signaling through a receptor complex shared by three different ligands. Our results provide unique insights into the complexity of IL-20SFC signaling that may be critical in the design of mechanistic-based inhibitors of IL-20SFC-mediated inflammatory disease."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.org/dc/terms/identifier"doi:10.1073/pnas.1117551109"xsd:string
http://purl.uniprot.org/citations/22802649http://purl.org/dc/terms/identifier"doi:10.1073/pnas.1117551109"xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/author"Rajashankar K.R."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/author"Rajashankar K.R."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/author"Logsdon N.J."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/author"Logsdon N.J."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/author"Walter M.R."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/author"Walter M.R."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/author"Deshpande A."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/author"Deshpande A."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/author"Harris B.D."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/author"Harris B.D."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/date"2012"xsd:gYear
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/date"2012"xsd:gYear
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/name"Proc. Natl. Acad. Sci. U.S.A."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/name"Proc. Natl. Acad. Sci. U.S.A."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/pages"12704-12709"xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/pages"12704-12709"xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/title"Structural basis for receptor sharing and activation by interleukin-20 receptor-2 (IL-20R2) binding cytokines."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/title"Structural basis for receptor sharing and activation by interleukin-20 receptor-2 (IL-20R2) binding cytokines."xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/volume"109"xsd:string
http://purl.uniprot.org/citations/22802649http://purl.uniprot.org/core/volume"109"xsd:string