N-Terminal Acetyltransferase F
"N-Terminal Acetyltransferase F" 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.
An N-terminal acetyltransferase subtype that consists of the Naa60p catalytic subunit. It is found in higher eukayotes and displays a substrate specificity for the N-terminal METHIONINE of peptides where the next amino acid in the chain is either LEUCINE; LYSINE; PHENYALANINE; ISOLEUCINE; or TRYPTOPHANE.
| Descriptor ID |
D063214
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| MeSH Number(s) |
D08.811.913.050.134.423.600
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| Concept/Terms |
N-Terminal Acetyltransferase F- N-Terminal Acetyltransferase F
- N Terminal Acetyltransferase F
- N-Terminal Acetyltransferase Type F
- N Terminal Acetyltransferase Type F
- NatF N-Terminal Acetyltransferase
- N-Terminal Acetyltransferase, NatF
- NatF N Terminal Acetyltransferase
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Below are MeSH descriptors whose meaning is more general than "N-Terminal Acetyltransferase F".
Below are MeSH descriptors whose meaning is more specific than "N-Terminal Acetyltransferase F".
This graph shows the total number of publications written about "N-Terminal Acetyltransferase F" by people in this website by year, and whether "N-Terminal Acetyltransferase F" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "N-Terminal Acetyltransferase F" by people in Profiles.
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Chelban V, Aksnes H, Maroofian R, LaMonica LC, Seabra L, Siggervåg A, Devic P, Shamseldin HE, Vandrovcova J, Murphy D, Richard AC, Quenez O, Bonnevalle A, Zanetti MN, Kaiyrzhanov R, Salpietro V, Efthymiou S, Schottlaender LV, Morsy H, Scardamaglia A, Tariq A, Pagnamenta AT, Pennavaria A, Krogstad LS, Bekkelund ÅK, Caiella A, Glomnes N, Brønstad KM, Tury S, Moreno De Luca A, Boland-Auge A, Olaso R, Deleuze JF, Anheim M, Cretin B, Vona B, Alajlan F, Abdulwahab F, Battini JL, Ipek R, Bauer P, Zifarelli G, Gungor S, Kurul SH, Lochmuller H, Da'as SI, Fakhro KA, Gómez-Pascual A, Botía JA, Wood NW, Horvath R, Ernst AM, Rothman JE, McEntagart M, Crow YJ, Alkuraya FS, Nicolas G, Arnesen T, Houlden H. Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications. Nat Commun. 2024 Mar 13; 15(1):2269.
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