Interaction of mitochondrial initiation factor 2 with mitochondrial fMet-tRNA.
about
Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translationRole of the N- and C-terminal extensions on the activity of mammalian mitochondrial translational initiation factor 3.Structure and Activity of Human Mitochondrial Peptide Deformylase, a Novel Cancer TargetMitochondrial translation initiation machinery: conservation and diversificationThe role of formylated peptides and formyl peptide receptor 1 in governing neutrophil function during acute inflammationALDH1L2 is the mitochondrial homolog of 10-formyltetrahydrofolate dehydrogenaseClinical and functional characterisation of the combined respiratory chain defect in two sisters due to autosomal recessive mutations in MTFMTInhibition of human peptide deformylase disrupts mitochondrial functionBiochemical characterization of pathogenic mutations in human mitochondrial methionyl-tRNA formyltransferaseAn N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase.Mitochondrial transcript maturation and its disordersMechanism of protein biosynthesis in mammalian mitochondria.High throughput gene complementation screening permits identification of a mammalian mitochondrial protein synthesis (ρ(-)) mutant.Structure-Based Drug Design of Small Molecule Peptide Deformylase Inhibitors to Treat Cancer.The interaction of mammalian mitochondrial translational initiation factor 3 with ribosomes: evolution of terminal extensions in IF3mt.Roles of the N- and C-terminal domains of mammalian mitochondrial initiation factor 3 in protein biosynthesis.FDH: an aldehyde dehydrogenase fusion enzyme in folate metabolism.Methylene tetrahydrofolate dehydrogenase/cyclohydrolase and the synthesis of 10-CHO-THF are essential in Leishmania major.The enzymes of the 10-formyl-tetrahydrofolate synthetic pathway are found exclusively in the cytosol of the trypanosomatid parasite Leishmania major.Protein biosynthesis in mitochondriaA disease-causing point mutation in human mitochondrial tRNAMet results in tRNA misfolding leading to defects in translational initiation and elongation.Kinetic modelling of mitochondrial translation.
P2860
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P2860
Interaction of mitochondrial initiation factor 2 with mitochondrial fMet-tRNA.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Interaction of mitochondrial initiation factor 2 with mitochondrial fMet-tRNA.
@en
type
label
Interaction of mitochondrial initiation factor 2 with mitochondrial fMet-tRNA.
@en
prefLabel
Interaction of mitochondrial initiation factor 2 with mitochondrial fMet-tRNA.
@en
P2860
P356
P1476
Interaction of mitochondrial initiation factor 2 with mitochondrial fMet-tRNA.
@en
P2093
Angela C Spencer
Linda L Spremulli
P2860
P304
P356
10.1093/NAR/GKH886
P577
2004-10-11T00:00:00Z