 Sequence Homology, Amino Acid
"Sequence Homology, Amino Acid" 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 degree of similarity between sequences of amino acids. This information is useful for the analyzing genetic relatedness of proteins and species.
| Descriptor ID |
D017386
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| MeSH Number(s) |
G02.111.810.200 G05.810.200
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| Concept/Terms |
Sequence Homology, Amino Acid- Sequence Homology, Amino Acid
- Sequence Homology, Protein
- Amino Acid Sequence Homology
- Homology, Protein Sequence
- Homologies, Protein Sequence
- Protein Sequence Homologies
- Sequence Homologies, Protein
- Protein Sequence Homology
Homologous Sequences, Amino Acid- Homologous Sequences, Amino Acid
- Protein Sequence Homologs
- Homologs, Amino Acid Sequence
- Homologs, Protein Sequence
- Homolog, Protein Sequence
- Protein Sequence Homolog
- Sequence Homolog, Protein
- Sequence Homologs, Protein
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Below are MeSH descriptors whose meaning is more general than "Sequence Homology, Amino Acid".
Below are MeSH descriptors whose meaning is more specific than "Sequence Homology, Amino Acid".
This graph shows the total number of publications written about "Sequence Homology, Amino Acid" by people in this website by year, and whether "Sequence Homology, Amino Acid" 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 |
|---|
| 1995 | 0 | 1 | 1 | | 1996 | 0 | 1 | 1 | | 1999 | 0 | 1 | 1 | | 2006 | 0 | 1 | 1 | | 2007 | 0 | 1 | 1 |
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Below are the most recent publications written about "Sequence Homology, Amino Acid" by people in Profiles.
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Thomas HR, Ezzeldin HH, Guarcello V, Mattison LK, Fridley BL, Diasio RB. Genetic regulation of dihydropyrimidinase and its possible implication in altered uracil catabolism. Pharmacogenet Genomics. 2007 Nov; 17(11):973-87.
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Sato H, Miyamoto T, Yogev L, Namiki M, Koh E, Hayashi H, Sasaki Y, Ishikawa M, Lamb DJ, Matsumoto N, Birk OS, Niikawa N, Sengoku K. Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest. J Hum Genet. 2006; 51(6):533-540.
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Magdaleno S, Northcutt GM, Curran T, Kurschner C. mPPP1R16B is a novel mouse protein phosphatase 1 targeting subunit whose mRNA is located in cell bodies and dendrites of neurons in four distinct regions of the brain. Brain Res Gene Expr Patterns. 2002 Oct; 1(3-4):143-9.
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Homayouni R, Rice DS, Curran T. Disabled-1 interacts with a novel developmentally regulated protocadherin. Biochem Biophys Res Commun. 2001 Nov 30; 289(2):539-47.
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Bartnikas TB, Waggoner DJ, Casareno RL, Gaedigk R, White RA, Gitlin JD. Chromosomal localization of CCS, the copper chaperone for Cu/Zn superoxide dismutase. Mamm Genome. 2000 May; 11(5):409-11.
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Hamza I, Klomp LW, Gaedigk R, White RA, Gitlin JD. Structure, expression, and chromosomal localization of the mouse Atox1 gene. Genomics. 2000 Jan 15; 63(2):294-7.
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Homayouni R, Rice DS, Sheldon M, Curran T. Disabled-1 binds to the cytoplasmic domain of amyloid precursor-like protein 1. J Neurosci. 1999 Sep 01; 19(17):7507-15.
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Soltysik-Espanola M, Rogers RA, Jiang S, Kim TA, Gaedigk R, White RA, Avraham H, Avraham S. Characterization of Mayven, a novel actin-binding protein predominantly expressed in brain. Mol Biol Cell. 1999 Jul; 10(7):2361-75.
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Brix LA, Duggleby RG, Gaedigk A, McManus ME. Structural characterization of human aryl sulphotransferases. Biochem J. 1999 Jan 15; 337 ( Pt 2):337-43.
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Talebizadeh Z, Kelley PM, Askew JW, Beisel KW, Smith SD. Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss. Hum Mutat. 1999; 14(6):493-501.
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