"Aminoacylation" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A reaction that introduces an aminoacyl group to a molecule. TRANSFER RNA AMINOACYLATION is the first step in GENETIC TRANSLATION.
Descriptor ID |
D049148
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MeSH Number(s) |
G02.111.012.055 G02.111.660.050 G02.607.063.526 G03.040.055 G03.734.050
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Concept/Terms |
Aminoacylation- Aminoacylation
- Aminoacylations
- Amino Acylation
- Acylation, Amino
- Acylations, Amino
- Amino Acylations
Activation of Amino Acids- Activation of Amino Acids
- Acids Activation, Amino
- Acids Activations, Amino
- Amino Acids Activation
- Amino Acids Activations
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Below are MeSH descriptors whose meaning is more general than "Aminoacylation".
Below are MeSH descriptors whose meaning is more specific than "Aminoacylation".
This graph shows the total number of publications written about "Aminoacylation" by people in this website by year, and whether "Aminoacylation" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2014 | 0 | 1 | 1 |
2017 | 0 | 1 | 1 |
2019 | 0 | 1 | 1 |
2021 | 0 | 1 | 1 |
2023 | 0 | 1 | 1 |
2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Aminoacylation" by people in Profiles.
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A potential role for RNA aminoacylation prior to its role in peptide synthesis. Proc Natl Acad Sci U S A. 2024 Aug 27; 121(35):e2410206121.
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Single-read tRNA-seq analysis reveals coordination of tRNA modification and aminoacylation and fragmentation. Nucleic Acids Res. 2023 02 22; 51(3):e17.
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CMT2N-causing aminoacylation domain mutants enable Nrp1 interaction with AlaRS. Proc Natl Acad Sci U S A. 2021 03 30; 118(13).
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CMT disease severity correlates with mutation-induced open conformation of histidyl-tRNA synthetase, not aminoacylation loss, in patient cells. Proc Natl Acad Sci U S A. 2019 09 24; 116(39):19440-19448.
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Determination of tRNA aminoacylation levels by high-throughput sequencing. Nucleic Acids Res. 2017 Aug 21; 45(14):e133.
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Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures. Am J Hum Genet. 2014 Apr 03; 94(4):547-58.