Reference on EC 2.1.1.61 - tRNA 5-(aminomethyl)-2-thiouridylate-methyltransferase
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REF. 
AUTHORS
TITLE
JOURNAL
VOL.
PAGES
YEAR
ORGANISM (UNIPROT)
PUBMED ID
SOURCE
Taya, Y.; Nishimura, S.
Biosynthesis of 5-methylaminomethyl-2-thiouridylate. I. Isolation of a new tRNA-methylase specific for 5-methylaminomethyl-2-thiouridylate
Biochem. Biophys. Res. Commun.
51
1062-1068
1973
Escherichia coli, Escherichia coli B / ATCC 11303
Hagervall, T.G.; Edmonds, C.G.; McCloskey, J.A.; Bjrk, G.R.
Transfer RNA(5-methylaminomethyl-2-thiouridine)-methyltransferase from Escherichia coli K-12 has two enzymatic activities
J. Biol. Chem.
262
8488-8495
1987
Escherichia coli
Hagervall, T.G.; Bjrk, G.R.
Genetic mapping and cloning of the gene (trmC) responsible for the synthesis of tRNA (mnm5s2U)methyltransferase in Escherichia coli K12
Mol. Gen. Genet.
196
201-207
1984
Escherichia coli
Yan, Q.; Guan, M.X.
Identification and characterization of mouse TRMU gene encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase
Biochim. Biophys. Acta
1676
119-126
2004
Mus musculus (Q9DAT5), Mus musculus
Yan, Q.; Bykhovskaya, Y.; Li, R.; Mengesha, E.; Shohat, M.; Estivill, X.; Fischel-Ghodsian, N.; Guan, M.X.
Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutations
Biochem. Biophys. Res. Commun.
342
1130-1136
2006
Homo sapiens (O75648), Homo sapiens
Zeharia, A.; Shaag, A.; Pappo, O.; Mager-Heckel, A.M.; Saada, A.; Beinat, M.; Karicheva, O.; Mandel, H.; Ofek, N.; Segel, R.; Marom, D.; Roetig, A.; Tarassov, I.; Elpeleg, O.
Acute infantile liver failure due to mutations in the TRMU gene
Am. J. Hum. Genet.
85
401-407
2009
Homo sapiens
Meng, F.; Cang, X.; Peng, Y.; Li, R.; Zhang, Z.; Li, F.; Fan, Q.; Guan, A.S.; Fischel-Ghosian, N.; Zhao, X.; Guan, M.X.
Biochemical evidence for a nuclear modifier allele (A10S) in TRMU (methylaminomethyl-2-thiouridylate-methyltransferase) related to mitochondrial tRNA modification in the phenotypic manifestation of deafness-associated 12S rRNA mutation
J. Biol. Chem.
292
2881-2892
2017
Homo sapiens
Grover, Z.; Lewindon, P.; Clousten, A.; Shaag, A.; Elpeleg, O.; Coman, D.
Hepatic copper accumulation a novel feature in transient infantile liver failure due to TRMU mutations?
JIMD Rep.
21
109-113
2015
Homo sapiens
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