N-Terminal Acetyltransferase A
"N-Terminal Acetyltransferase A" 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 Naa10p catalytic subunit and the Naa15p auxiliary subunit. The structure of this enzyme is conserved between lower and higher eukaryotes. It has specificity for N-terminal SERINE; ALANINE; THREONINE; GLYCINE; VALINE; and CYSTINE residues and acts on nascent peptide chains after the removal of the initiator METHIONINE by METHIONYL AMINOPEPTIDASES.
| Descriptor ID |
D063209
|
| MeSH Number(s) |
D08.811.913.050.134.423.100
|
| Concept/Terms |
N-Terminal Acetyltransferase A- N-Terminal Acetyltransferase A
- N Terminal Acetyltransferase A
- NatA N-Terminal Acetyltransferase
- N-Terminal Acetyltransferase, NatA
- NatA N Terminal Acetyltransferase
- N-Terminal Acetyltransferase Type A
- N Terminal Acetyltransferase Type A
|
Below are MeSH descriptors whose meaning is more general than "N-Terminal Acetyltransferase A".
Below are MeSH descriptors whose meaning is more specific than "N-Terminal Acetyltransferase A".
This graph shows the total number of publications written about "N-Terminal Acetyltransferase A" by people in UAMS Profiles by year, and whether "N-Terminal Acetyltransferase A" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "N-Terminal Acetyltransferase A" by people in Profiles over the past ten years.
-
St?ve SI, Blenski M, Stray-Pedersen A, Wierenga KJ, Jhangiani SN, Akdemir ZC, Crawford D, McTiernan N, Myklebust LM, Purcarin G, McNall-Knapp R, Wadley A, Belmont JW, Kim JJ, Lupski JR, Arnesen T. A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy. Eur J Hum Genet. 2018 09; 26(9):1294-1305.