Cargando…
More Than One HMG-CoA Lyase: The Classical Mitochondrial Enzyme Plus the Peroxisomal and the Cytosolic Ones
There are three human enzymes with HMG-CoA lyase activity that are able to synthesize ketone bodies in different subcellular compartments. The mitochondrial HMG-CoA lyase was the first to be described, and catalyzes the cleavage of 3-hydroxy-3-methylglutaryl CoA to acetoacetate and acetyl-CoA, the c...
Autores principales: | Arnedo, María, Latorre-Pellicer, Ana, Lucia-Campos, Cristina, Gil-Salvador, Marta, Antoñanzas-Peréz, Rebeca, Gómez-Puertas, Paulino, Bueno-Lozano, Gloria, Puisac, Beatriz, Pié, Juan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941031/ https://www.ncbi.nlm.nih.gov/pubmed/31817290 http://dx.doi.org/10.3390/ijms20246124 |
Ejemplares similares
-
Characterization of a novel HMG-CoA lyase enzyme with a dual location in endoplasmic reticulum and cytosol
por: Arnedo, María, et al.
Publicado: (2012) -
Differential HMG-CoA lyase expression in human tissues provides clues about 3-hydroxy-3-methylglutaric aciduria
por: Puisac, Beatriz, et al.
Publicado: (2010) -
Human Mitochondrial HMG-CoA Synthase Deficiency: Role of Enzyme Dimerization Surface and Characterization of Three New Patients
por: Puisac, Beatriz, et al.
Publicado: (2018) -
Things are not always what they seem: From Cornelia de Lange to KBG phenotype in a girl with genetic variants in NIPBL and ANKRD11
por: Latorre‐Pellicer, Ana, et al.
Publicado: (2021) -
Evaluating Face2Gene as a Tool to Identify Cornelia de Lange Syndrome by Facial Phenotypes
por: Latorre-Pellicer, Ana, et al.
Publicado: (2020)