Amino Acid Sequence
"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
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MeSH Number(s) |
G02.111.570.060 L01.453.245.667.060
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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
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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 |
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1980 | 0 | 1 | 1 | 1984 | 0 | 3 | 3 | 1985 | 0 | 4 | 4 | 1986 | 0 | 4 | 4 | 1987 | 0 | 2 | 2 | 1988 | 0 | 3 | 3 | 1989 | 0 | 2 | 2 | 1990 | 0 | 8 | 8 | 1991 | 0 | 4 | 4 | 1992 | 0 | 7 | 7 | 1993 | 0 | 5 | 5 | 1994 | 0 | 4 | 4 | 1995 | 0 | 9 | 9 | 1996 | 0 | 9 | 9 | 1997 | 0 | 14 | 14 | 1998 | 0 | 9 | 9 | 1999 | 0 | 13 | 13 | 2000 | 1 | 11 | 12 | 2001 | 0 | 8 | 8 | 2002 | 0 | 19 | 19 | 2003 | 0 | 12 | 12 | 2004 | 0 | 14 | 14 | 2005 | 1 | 12 | 13 | 2006 | 0 | 11 | 11 | 2007 | 1 | 12 | 13 | 2008 | 0 | 8 | 8 | 2009 | 0 | 9 | 9 | 2010 | 1 | 6 | 7 | 2011 | 0 | 8 | 8 | 2012 | 0 | 8 | 8 | 2013 | 0 | 4 | 4 | 2014 | 0 | 4 | 4 | 2015 | 0 | 8 | 8 | 2016 | 0 | 3 | 3 | 2017 | 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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Kilpatrick LE, Friedman-Ohana R, Alcobia DC, Riching K, Peach CJ, Wheal AJ, Briddon SJ, Robers MB, Zimmerman K, Machleidt T, Wood KV, Woolard J, Hill SJ. Real-time analysis of the binding of fluorescent VEGF165a to VEGFR2 in living cells: Effect of receptor tyrosine kinase inhibitors and fate of internalized agonist-receptor complexes. Biochem Pharmacol. 2017 Jul 15; 136:62-75.
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Smith IN, Briggs JM. Structural mutation analysis of PTEN and its genotype-phenotype correlations in endometriosis and cancer. Proteins. 2016 Nov; 84(11):1625-1643.
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Shen Y, Liu M, Wang L, Li Z, Taylor DC, Li Z, Zhang M. Identification, duplication, evolution and expression analyses of caleosins in Brassica plants and Arabidopsis subspecies. Mol Genet Genomics. 2016 Apr; 291(2):971-88.
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Kanan Y, Al-Ubaidi MR. Identification of Tyrosine O Sulfated Proteins in Cow Retina and the 661W Cell Line. Adv Exp Med Biol. 2016; 854:649-54.
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Canning P, Ruan Q, Schwerd T, Hrdinka M, Maki JL, Saleh D, Suebsuwong C, Ray S, Brennan PE, Cuny GD, Uhlig HH, Gyrd-Hansen M, Degterev A, Bullock AN. Inflammatory Signaling by NOD-RIPK2 Is Inhibited by Clinically Relevant Type II Kinase Inhibitors. Chem Biol. 2015 Sep 17; 22(9):1174-84.
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Storer Samaniego C, Suh JH, Chattopadhyay A, Olivares K, Guy N, Sivils JC, Dey P, Yumoto F, Fletterick RJ, Strom AM, Gustafsson JÅ, Webb P, Cox MB. The FKBP52 Cochaperone Acts in Synergy with ß-Catenin to Potentiate Androgen Receptor Signaling. PLoS One. 2015; 10(7):e0134015.
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Hoffmann C, Castro M, Rinken A, Leurs R, Hill SJ, Vischer HF. Ligand Residence Time at G-protein-Coupled Receptors-Why We Should Take Our Time To Study It. Mol Pharmacol. 2015 Sep; 88(3):552-60.
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Orhan E, Dalkara D, Neuillé M, Lechauve C, Michiels C, Picaud S, Léveillard T, Sahel JA, Naash MI, Lavail MM, Zeitz C, Audo I. Genotypic and phenotypic characterization of P23H line 1 rat model. PLoS One. 2015; 10(5):e0127319.
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Kim Y, Makowska-Grzyska M, Gorla SK, Gollapalli DR, Cuny GD, Joachimiak A, Hedstrom L. Structure of Cryptosporidium IMP dehydrogenase bound to an inhibitor with in vivo antiparasitic activity. Acta Crystallogr F Struct Biol Commun. 2015 May; 71(Pt 5):531-8.
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Najjar M, Suebsuwong C, Ray SS, Thapa RJ, Maki JL, Nogusa S, Shah S, Saleh D, Gough PJ, Bertin J, Yuan J, Balachandran S, Cuny GD, Degterev A. Structure guided design of potent and selective ponatinib-based hybrid inhibitors for RIPK1. Cell Rep. 2015 Mar 24; 10(11):1850-60.
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