GO_REF:0000002
Gene Ontology annotation through association of InterPro records with GO terms
GO_REF:0000024
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000044
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
GO_REF:0000117
Electronic Gene Ontology annotations created by ARBA machine learning models
PMID:22658674
Insights into RNA biology from an atlas of mammalian mRNA-binding proteins.
PMID:22681889
The mRNA-bound proteome and its global occupancy profile on protein-coding transcripts.
PMID:25838379
Ribosome. The structure of the human mitochondrial ribosome.
PMID:27023846
Structure and Function of the Mitochondrial Ribosome.
PMID:34800366
Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context.
Reactome:R-HSA-5419261
55S ribosome with peptidyl-tRNA in A site binds GFM1:GTP
Reactome:R-HSA-5419264
MTRF1L (MTRF1a) or ICT1 binds stop codon in 55S ribosome:mRNA:peptidyl-tRNA
Reactome:R-HSA-5419271
55S ribosome:MTRF1L hydrolyzes peptidyl-tRNA bond and GTP is hydrolyzed
Reactome:R-HSA-5419273
Hydrolysis of GTP and dissociation of 28S and 39S subunits
Reactome:R-HSA-5419277
GFM2:GTP binds 55S ribosome:mRNA:tRNA:MRRF releasing mRNA and tRNA
Reactome:R-HSA-5419281
MRRF binds 55S ribosome:mRNA:tRNA
Reactome:R-HSA-9937394
55S ribosome:MTRF1 hydrolyzes peptidyl-tRNA bond and GTP is hydrolyzed
Reactome:R-HSA-9937412
Stalled 55S mitochondrial ribosome is dissociated to yield 28S subunit and 39S subunit:mRNA:peptidyl-tRNA:tRNA
Reactome:R-HSA-9937415
MTRF1 and GTP bind 55S ribosome:MT-CO1,MT-ND6 mRNA:peptidyl-tRNA at P-site:tRNA at E-site
Reactome:R-HSA-9937719
ICT1 hydrolyzes the peptidyl-tRNA bond of the nascent polypeptide
Reactome:R-HSA-9937724
55S mitochondrial ribosome:non-stop mRNA binds ICT1 (MRPL58)
PMID:25556185
Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia.