=
Note: Conversion is based on the latest values and formulas.
Aspartylglucosaminidase - Wikipedia N (4)- (beta-N-acetylglucosaminyl)-L-asparaginase is an enzyme that in humans is encoded by the AGA gene. [5] Aspartylglucosaminidase is an amidohydrolase enzyme involved in the catabolism of N-linked oligosaccharides of glycoproteins.
Structural basis of aspartylglucosaminuria - ScienceDirect 26 Dec 2008 · Aspartylglucosaminidase (AGA, EC 3.5.1.26) is a lysosomal amidase which plays a role in cleavage of the bonds between an asparagine and an N -acetylglucosamine, and is involved in the degradation of glycoproteins within lysosomes.
Aspartylglucosaminuria, AGU - The Medical Biochemistry Page 1 May 2024 · The N-aspartyl-β-glucosaminidase enzyme is encoded by the AGA gene. The AGA gene is located on chromosome 4q34.3 spanning 13kbp and composed of 9 exons that generate two alternatively spliced mRNAs. These mRNAs encode a 346 amino acid precursor protein (isoform 1) and a 336 amino acid precursor protein (isoform 2).
Nucleotides, codons & amino acids - HGVS Amino acid descriptions. For the complete and official list with further details go to IUPAC-IUBMB site. (NOTE: Formula-images copied from this site)
Functional analyses of active site residues of human lysosomal ... 17 Jun 1996 · Aspartylglucosaminidase (AGA) is a lysosomal asparaginase that participates in the breakdown of glycoproteins by cleaving the amide bond between the asparagine and the oligosaccharide chain.
Molecular pathogenesis of a disease: structural consequences of ... 15 Apr 2001 · Some AGU mutations hit highly conserved amino acids. The nucleophile of AGA, T206, residing in the N-terminus of the β-subunit, is fully conserved across the species (Fig. 2). Other active site residues show high conservation levels as well, but the lysosomal targeting residues, glycosylation sites, and disulfide bridge-forming residues (C64 ...
Nucleic Acids, Protein Synthesis, and Molecular Genetics 4 Apr 1997 · Aspartylglucosaminidase (AGA) is a lysosomal enzyme that catalyzes one of the final steps in the degradation of N-linked glycoproteins. Here we have analyzed the tissue-specific expression and regulation of the human and mouse AGA genes.
Codons and amino acids - HGVS amino acid descriptions - one / three letter code; amino acid properties; PAM-matrix
AGA Enzyme Human | Aspartylglucosaminidase - ProSpec Aspartylglucosaminidase, also known as AGA, takes part in the catabolism of Nlinked oligosaccharides of glycoproteins. AGA is a protein coding gene which cleaves asparagine from N-acetylglucosamines in the lysosomal breakdown of glycoproteins.
Codons Encoding Arginine: Unraveling the Amino Acid's Genetic Code 11 Sep 2024 · Through extensive research, scientists have identified three codons that encode the amino acid arginine: UCG, AGA, and AGG. These codons serve as the molecular blueprints for incorporating arginine into the growing protein chain during translation.
AGA gene - MedlinePlus The AGA gene provides instructions for producing an enzyme called aspartylglucosaminidase. This enzyme is active in lysosomes, which are structures inside cells that act as recycling centers.
AGA gene - MedlinePlus Most AGA gene variants change one amino acid in aspartylglucosaminidase. One variant, found in 98 percent of people with this condition in Finland, replaces the amino acid cysteine with the amino acid serine at position 163 in the enzyme (written as Cys163Ser or C163S).
Activation and Oligomerization of Aspartylglucosaminidase 25 Sep 1998 · We have recently determined the three-dimensional structure of lysosomal aspartylglucosaminidase (AGA), which belongs to a newly discovered family of homologous amidohydrolases, the N-terminal nucleophile hydrolases.
The importance of arginine codons AGA and AGG for the … 8 Jan 2017 · Rare arginine codons AGA and AGG affect the heterologous expression of proteins in Eschericha coli. The tRNAs necessary for protein synthesis are scarce in E. coli strain BL21 (DE3) pLysS and plentiful in strain BL21 (DE3) CodonPlus −RIL.
Entry - *613228 - ASPARTYLGLUCOSAMINIDASE; AGA - OMIM Aspartylglucosaminidase (AGA; EC 3.5.1.26) is a key enzyme in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves the asparagine from the residual N-acetylglucosamines as one of the final steps in the lysosomal breakdown …
The importance of arginine codons AGA and AGG for the … 1 Mar 2017 · Rare arginine codons AGA and AGG affect the heterologous expression of proteins in Eschericha coli. The tRNAs necessary for protein synthesis are scarce in E. coli strain BL21 (DE3) pLysS and plentiful in strain BL21 (DE3) CodonPlus −RIL.
Emergent rules for codon choice elucidated by editing rare arginine ... 20 Sep 2016 · The degeneracy of the genetic code allows nucleic acids to encode amino acid identity as well as noncoding information for gene regulation and genome maintenance. The rare arginine codons AGA and AGG (AGR) present a case study in codon choice, with AGRs encoding important transcriptional and transla …
Expression and Regulation of the Human and Mouse ... Aspartylglucosaminidase (AGA) is a lysosomal enzyme that catalyzes one of the final steps in the degradation of N-linked glycoproteins. Here we have analyzed the tissue-specific expression and regulation of the human and mouse AGA genes. We isolated and characterized human and mouse AGA 5′-flanking sequences including the promoter regions.
Amino Acid and Codon Table - UCSC I n this table, the twenty amino acids found in proteins are listed, along with the single-letter code used to represent these amino acids in protein data bases. The DNA codons representing each amino acid are also listed.