"Amino Acid Sequence" 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.
The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.
| Descriptor ID |
D000595
|
| MeSH Number(s) |
G02.111.570.060 L01.453.245.667.060
|
| Concept/Terms |
Amino Acid Sequence- Amino Acid Sequence
- Protein Structure, Primary
- Primary Protein Structure
- Primary Protein Structures
- Protein Structures, Primary
- Structure, Primary Protein
- Structures, Primary Protein
- Sequences, Amino Acid
- Amino Acid Sequences
- Sequence, Amino Acid
|
Below are MeSH descriptors whose meaning is more general than "Amino Acid Sequence".
Below are MeSH descriptors whose meaning is more specific than "Amino Acid Sequence".
This graph shows the total number of publications written about "Amino Acid Sequence" by people in this website by year, and whether "Amino Acid Sequence" 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 |
|---|
| 1994 | 0 | 4 | 4 |
| 1995 | 0 | 4 | 4 |
| 1996 | 0 | 5 | 5 |
| 1997 | 1 | 9 | 10 |
| 1998 | 0 | 1 | 1 |
| 1999 | 0 | 5 | 5 |
| 2000 | 0 | 5 | 5 |
| 2001 | 0 | 8 | 8 |
| 2002 | 0 | 2 | 2 |
| 2003 | 0 | 11 | 11 |
| 2004 | 0 | 4 | 4 |
| 2005 | 0 | 2 | 2 |
| 2006 | 0 | 7 | 7 |
| 2007 | 0 | 3 | 3 |
| 2008 | 0 | 7 | 7 |
| 2009 | 0 | 10 | 10 |
| 2010 | 0 | 5 | 5 |
| 2011 | 0 | 7 | 7 |
| 2012 | 0 | 13 | 13 |
| 2013 | 0 | 10 | 10 |
| 2014 | 0 | 9 | 9 |
| 2015 | 0 | 12 | 12 |
| 2016 | 0 | 5 | 5 |
| 2017 | 0 | 5 | 5 |
| 2018 | 0 | 2 | 2 |
| 2019 | 0 | 4 | 4 |
| 2020 | 0 | 1 | 1 |
| 2021 | 0 | 3 | 3 |
| 2023 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Amino Acid Sequence" by people in Profiles.
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Whole genome analysis of two sympatric human Mansonella: Mansonella perstans and Mansonella sp "DEUX". Front Cell Infect Microbiol. 2023; 13:1159814.
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Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome. J Am Soc Nephrol. 2021 03; 32(3):580-596.
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Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1-Associated Diseases. Genes (Basel). 2021 01 21; 12(2).
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Longitudinal high-throughput TCR repertoire profiling reveals the dynamics of T-cell memory formation after mild COVID-19 infection. Elife. 2021 01 05; 10.
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CASC3 promotes transcriptome-wide activation of nonsense-mediated decay by the exon junction complex. Nucleic Acids Res. 2020 09 04; 48(15):8626-8644.
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Complementing the intrinsic repertoire of Ustilago maydis for degradation of the pectin backbone polygalacturonic acid. J Biotechnol. 2020 Jan 10; 307:148-163.
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Low mutational load in pediatric medulloblastoma still translates into neoantigens as targets for specific T-cell immunotherapy. Cytotherapy. 2019 09; 21(9):973-986.
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Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma. Nat Commun. 2019 03 29; 10(1):1459.
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Smut infection of perennial hosts: the genome and the transcriptome of the Brassicaceae smut fungus Thecaphora thlaspeos reveal functionally conserved and novel effectors. New Phytol. 2019 05; 222(3):1474-1492.
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Recessive mutations in the neuronal isoforms of DST, encoding dystonin, lead to abnormal actin cytoskeleton organization and HSAN type VI. Hum Mutat. 2019 01; 40(1):106-114.
MeSH information
