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http://purl.uniprot.org/citations/33670179http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/33670179http://www.w3.org/2000/01/rdf-schema#comment"Fumarylacetoacetate hydrolase (FAH) is the fifth enzyme in the tyrosine catabolism pathway. A deficiency in human FAH leads to hereditary tyrosinemia type I (HT1), an autosomal recessive disorder that results in the accumulation of toxic metabolites such as succinylacetone, maleylacetoacetate, and fumarylacetoacetate in the liver and kidney, among other tissues. The disease is severe and, when untreated, it can lead to death. A low tyrosine diet combined with the herbicidal nitisinone constitutes the only available therapy, but this treatment is not devoid of secondary effects and long-term complications. In this study, we targeted FAH for the first-time to discover new chemical modulators that act as pharmacological chaperones, directly associating with this enzyme. After screening several thousand compounds and subsequent chemical redesign, we found a set of reversible inhibitors that associate with FAH close to the active site and stabilize the (active) dimeric species, as demonstrated by NMR spectroscopy. Importantly, the inhibitors are also able to partially restore the normal phenotype in a newly developed cellular model of HT1."xsd:string
http://purl.uniprot.org/citations/33670179http://purl.org/dc/terms/identifier"doi:10.3390/ijms22041789"xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/author"Mato J.M."xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/author"Millet O."xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/author"Lopitz-Otsoa F."xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/author"Lain A."xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/author"Sanz-Parra A."xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/author"Gil-Martinez J."xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/author"Bernardo-Seisdedos G."xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/author"Macias I."xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/author"Fernandez-Ramos D."xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/author"Unione L."xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/name"Int J Mol Sci"xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/pages"1789"xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/title"Therapeutic Targeting of Fumaryl Acetoacetate Hydrolase in Hereditary Tyrosinemia Type I."xsd:string
http://purl.uniprot.org/citations/33670179http://purl.uniprot.org/core/volume"22"xsd:string
http://purl.uniprot.org/citations/33670179http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/33670179
http://purl.uniprot.org/citations/33670179http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/33670179
http://purl.uniprot.org/uniprot/#_A0A384P5L6-mappedCitation-33670179http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33670179
http://purl.uniprot.org/uniprot/#_B7Z4W2-mappedCitation-33670179http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33670179
http://purl.uniprot.org/uniprot/#_P16930-mappedCitation-33670179http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33670179
http://purl.uniprot.org/uniprot/#_P35505-mappedCitation-33670179http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33670179
http://purl.uniprot.org/uniprot/A0A384P5L6http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/33670179