"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
|
| MeSH Number(s) |
G02.111.012.055 G02.111.660.050 G02.607.063.526 G03.040.055 G03.734.050
|
| 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
|
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 |
|---|
| 2008 | 0 | 1 | 1 |
| 2011 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
| 2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Aminoacylation" by people in Profiles.
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Coordination between aminoacylation and editing to protect against proteotoxicity. Nucleic Acids Res. 2023 10 27; 51(19):10606-10618.
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Structural basis of amino acid surveillance by higher-order tRNA-mRNA interactions. Nat Struct Mol Biol. 2019 12; 26(12):1094-1105.
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Kinetic and structural changes in HsmtPheRS, induced by pathogenic mutations in human FARS2. Protein Sci. 2017 Aug; 26(8):1505-1516.
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Unique domain appended to vertebrate tRNA synthetase is essential for vascular development. Nat Commun. 2012 Feb 21; 3:681.
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An exit cavity was crucial to the polymerase activity of the early ribosome. Astrobiology. 2012 Jan; 12(1):57-60.
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A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N). Hum Mutat. 2012 Jan; 33(1):244-53.
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Following translation by single ribosomes one codon at a time. Nature. 2008 Apr 03; 452(7187):598-603.
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In vitro translation of STNV-RNA. Methods Enzymol. 1974; 30:754-61.