"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,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2002 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2014 | 0 | 1 | 1 |
| 2015 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Amino Acid Sequence" by people in Profiles.
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Stereospecific control of peptide gas-phase ion chemistry with cis and trans cyclo ornithine residues. J Mass Spectrom. 2018 Feb; 53(2):124-137.
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Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nat Genet. 2017 09; 49(9):1373-1384.
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A novel CHST3 allele associated with spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred. Clin Genet. 2016 07; 90(1):90-5.
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Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes. J Med Genet. 2015 Feb; 52(2):85-94.
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Coding variants in TREM2 increase risk for Alzheimer's disease. Hum Mol Genet. 2014 Nov 01; 23(21):5838-46.
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Association of the VDR translation start site polymorphism and fracture risk in older women. J Bone Miner Res. 2007 May; 22(5):730-6.
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Myelin basic protein: a multifunctional protein. Cell Mol Life Sci. 2006 Sep; 63(17):1945-61.
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Subthreshold changes of voltage-dependent activation of the K(V)7.2 channel in neonatal epilepsy. Neurobiol Dis. 2006 Oct; 24(1):194-201.
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Associations between measles antibody levels and the protein structure of class II human leukocyte antigens. Hum Immunol. 2003 Jul; 64(7):696-707.
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Late pregnancy suppresses relapses in experimental autoimmune encephalomyelitis: evidence for a suppressive pregnancy-related serum factor. J Immunol. 2002 Jul 15; 169(2):1084-91.