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AttributesValues
rdf:type
rdfs:label
  • CFTR Pathway
rdfs:subClassOf
Semantic_Type
  • Functional Concept
Preferred_Name
  • CFTR Pathway
UMLS_CUI
  • C1511437
BioCarta_ID
  • h_cftrPathway
ALT_DEFINITION
  • The defects in cAMP-regulated chloride channel CTFR are believed to be the major cause for cystic fibrosis. Regulation of CFTR protein by the surface receptor beta adrenergic receptor is mediated through the ezrin/radixin/moesin binding phosphoprotein 50 (EBP50), which binds both the C-termini CFTR and b2AR through their PDZ binding motifs. In the resting state, CFTR, b2AR, and EBP50 exist as a macromolecular complex on the apical surface of epithelial cells. Upon agonist activation of the b2AR, the adenylate cyclase is stimulated through the G protein pathway, leading to an increase in cAMP. The elevated concentration of cAMP activates PKA, which is anchored near CFTR via interaction with Ezrin. The phosphorylation of CFTR by PKA disrupts the complex and leads to compartmentalized and specific signaling of the channel.BIOCARTA
Legacy_Concept_Name
  • CFTR_Pathway
FULL_SYN
  • CFTR PathwayPTNCI
  • Cystic fibrosis transmembrane conductance regulator (CFTR) and beta 2 adrenergic receptor (b2AR) pathwayPTBIOCARTA
code
  • C39027
is someValuesFrom of
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