Pathogenic variants in glutamyl-tRNAGln amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder
Abstract Mitochondrial protein synthesis requires charging mt-tRNAs with their cognate amino acids by mitochondrial aminoacyl-tRNA synthetases, with the exception of glutaminyl mt-tRNA (mt-tRNAGln). mt-tRNAGln is indirectly charged by a transamidation reaction involving the GatCAB aminoacyl-tRNA ami...
Similar Items
-
Translation in amino-acid-poor environments is limited by tRNAGln charging
by: Natalya N Pavlova, et al.
Published: (2020-12-01) -
Mitochondrial encephalopathy Due to a Novel Pathogenic Mitochondrial tRNAGln m.4349C>T Variant
by: Kunqian Ji, et al.
Published: (2020-06-01) -
Purification of formylglycinamide ribotide amidotransferase from chicken liver.
by: Mizobuchi, Kiyoshi.
Published: (2024) -
Formylglycinamide Ribonucleotide Amidotransferase from Thermotoga maritima: Structural Insights into Complex Formation
by: Morar, Mariya, et al.
Published: (2012) -
Structure of the essential peptidoglycan amidotransferase MurT/GatD complex from Streptococcus pneumoniae
by: Cécile Morlot, et al.
Published: (2018-08-01)