A non-essential amino acid that is involved in the metabolic control of cell functions in nerve and brain tissue. It is biosynthesized from ASPARTIC ACID and AMMONIA by asparagine synthetase. (From Concise Encyclopedia Biochemistry and Molecular Biology, 3rd ed)
An enzyme that catalyzes the formation of asparagine from ammonia and aspartic acid, in the presence of ATP. EC 6.3.1.1.
A hydrolase enzyme that converts L-asparagine and water to L-aspartate and NH3. EC 3.5.1.1.
One of the non-essential amino acids commonly occurring in the L-form. It is found in animals and plants, especially in sugar cane and sugar beets. It may be a neurotransmitter.
A non-essential amino acid present abundantly throughout the body and is involved in many metabolic processes. It is synthesized from GLUTAMIC ACID and AMMONIA. It is the principal carrier of NITROGEN in the body and is an important energy source for many cells.
An amidohydrolase that removes intact asparagine-linked oligosaccharide chains from glycoproteins. It requires the presence of more than two amino-acid residues in the substrate for activity. This enzyme was previously listed as EC 3.2.2.18.
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.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
An enzyme that activates aspartic acid with its specific transfer RNA. EC 6.1.1.12.
A transfer RNA which is specific for carrying asparagine to sites on the ribosomes in preparation for protein synthesis.
Organic compounds that generally contain an amino (-NH2) and a carboxyl (-COOH) group. Twenty alpha-amino acids are the subunits which are polymerized to form proteins.
Genetically engineered MUTAGENESIS at a specific site in the DNA molecule that introduces a base substitution, or an insertion or deletion.
The chemical or biochemical addition of carbohydrate or glycosyl groups to other chemicals, especially peptides or proteins. Glycosyl transferases are used in this biochemical reaction.
A class of enzymes that catalyze the formation of a bond between two substrate molecules, coupled with the hydrolysis of a pyrophosphate bond in ATP or a similar energy donor. (Dorland, 28th ed) EC 6.
Enzymes that catalyze the joining of glutamine-derived ammonia and another molecule. The linkage is in the form of a carbon-nitrogen bond. EC 6.3.5.
Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations.
The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence.
An ASPARTIC ACID residue in polypeptide chains that is linked at the beta-carboxyl group instead of at the normal, alpha-carboxyl group, polypeptide linkage. It is a result of the spontaneous decomposition of aspartic acid or ASPARAGINE residues.
The rate dynamics in chemical or physical systems.
The naturally occurring or experimentally induced replacement of one or more AMINO ACIDS in a protein with another. If a functionally equivalent amino acid is substituted, the protein may retain wild-type activity. Substitution may also diminish, enhance, or eliminate protein function. Experimentally induced substitution is often used to study enzyme activities and binding site properties.
The parts of a macromolecule that directly participate in its specific combination with another molecule.
Enzymes that catalyze the transfer of nitrogenous groups, primarily amino groups, from a donor, generally an amino acid, to an acceptor, usually a 2-oxoacid. EC 2.6.
Models used experimentally or theoretically to study molecular shape, electronic properties, or interactions; includes analogous molecules, computer-generated graphics, and mechanical structures.
A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc.
An essential amino acid that is required for the production of HISTAMINE.
The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups.
The degree of similarity between sequences of amino acids. This information is useful for the analyzing genetic relatedness of proteins and species.
A characteristic feature of enzyme activity in relation to the kind of substrate on which the enzyme or catalytic molecule reacts.
Carbohydrates consisting of between two (DISACCHARIDES) and ten MONOSACCHARIDES connected by either an alpha- or beta-glycosidic link. They are found throughout nature in both the free and bound form.
Proteins which contain carbohydrate groups attached covalently to the polypeptide chain. The protein moiety is the predominant group with the carbohydrate making up only a small percentage of the total weight.
The facilitation of a chemical reaction by material (catalyst) that is not consumed by the reaction.
The characteristic 3-dimensional shape of a protein, including the secondary, supersecondary (motifs), tertiary (domains) and quaternary structure of the peptide chain. PROTEIN STRUCTURE, QUATERNARY describes the conformation assumed by multimeric proteins (aggregates of more than one polypeptide chain).
Proteins prepared by recombinant DNA technology.
A colorless alkaline gas. It is formed in the body during decomposition of organic materials during a large number of metabolically important reactions. Note that the aqueous form of ammonia is referred to as AMMONIUM HYDROXIDE.
The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells.
The sequence of carbohydrates within POLYSACCHARIDES; GLYCOPROTEINS; and GLYCOLIPIDS.
Organic compounds containing the -CO-NH2 radical. Amides are derived from acids by replacement of -OH by -NH2 or from ammonia by the replacement of H by an acyl group. (From Grant & Hackh's Chemical Dictionary, 5th ed)
The removal of an amino group (NH2) from a chemical compound.
The level of protein structure in which combinations of secondary protein structures (alpha helices, beta sheets, loop regions, and motifs) pack together to form folded shapes called domains. Disulfide bridges between cysteines in two different parts of the polypeptide chain along with other interactions between the chains play a role in the formation and stabilization of tertiary structure. Small proteins usually consist of only one domain but larger proteins may contain a number of domains connected by segments of polypeptide chain which lack regular secondary structure.
An element with the atomic symbol N, atomic number 7, and atomic weight [14.00643; 14.00728]. Nitrogen exists as a diatomic gas and makes up about 78% of the earth's atmosphere by volume. It is a constituent of proteins and nucleic acids and found in all living cells.
The largest class of organic compounds, including STARCH; GLYCOGEN; CELLULOSE; POLYSACCHARIDES; and simple MONOSACCHARIDES. Carbohydrates are composed of carbon, hydrogen, and oxygen in a ratio of Cn(H2O)n.
The normality of a solution with respect to HYDROGEN ions; H+. It is related to acidity measurements in most cases by pH = log 1/2[1/(H+)], where (H+) is the hydrogen ion concentration in gram equivalents per liter of solution. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
Any of various enzymatically catalyzed post-translational modifications of PEPTIDES or PROTEINS in the cell of origin. These modifications include carboxylation; HYDROXYLATION; ACETYLATION; PHOSPHORYLATION; METHYLATION; GLYCOSYLATION; ubiquitination; oxidation; proteolysis; and crosslinking and result in changes in molecular weight and electrophoretic motility.
Established cell cultures that have the potential to propagate indefinitely.
Liquid chromatographic techniques which feature high inlet pressures, high sensitivity, and high speed.
Intermediates in protein biosynthesis. The compounds are formed from amino acids, ATP and transfer RNA, a reaction catalyzed by aminoacyl tRNA synthetase. They are key compounds in the genetic translation process.
Members of the class of compounds composed of AMINO ACIDS joined together by peptide bonds between adjacent amino acids into linear, branched or cyclical structures. OLIGOPEPTIDES are composed of approximately 2-12 amino acids. Polypeptides are composed of approximately 13 or more amino acids. PROTEINS are linear polypeptides that are normally synthesized on RIBOSOMES.
A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
The characteristic 3-dimensional shape of a carbohydrate.
A low-energy attractive force between hydrogen and another element. It plays a major role in determining the properties of water, proteins, and other compounds.
The arrangement of two or more amino acid or base sequences from an organism or organisms in such a way as to align areas of the sequences sharing common properties. The degree of relatedness or homology between the sequences is predicted computationally or statistically based on weights assigned to the elements aligned between the sequences. This in turn can serve as a potential indicator of the genetic relatedness between the organisms.
A mutation caused by the substitution of one nucleotide for another. This results in the DNA molecule having a change in a single base pair.
Electrophoresis in which a polyacrylamide gel is used as the diffusion medium.
A modified nucleoside which is present in the first position of the anticodon of tRNA-tyrosine, tRNA-histidine, tRNA-asparagine and tRNA-aspartic acid of many organisms. It is believed to play a role in the regulatory function of tRNA. Nucleoside Q can be further modified to nucleoside Q*, which has a mannose or galactose moiety linked to position 4 of its cyclopentenediol moiety.
The process in which substances, either endogenous or exogenous, bind to proteins, peptides, enzymes, protein precursors, or allied compounds. Specific protein-binding measures are often used as assays in diagnostic assessments.
The study of crystal structure using X-RAY DIFFRACTION techniques. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Partial proteins formed by partial hydrolysis of complete proteins or generated through PROTEIN ENGINEERING techniques.
A colorless, odorless, highly water soluble vinyl monomer formed from the hydration of acrylonitrile. It is primarily used in research laboratories for electrophoresis, chromatography, and electron microscopy and in the sewage and wastewater treatment industries.
A transfer RNA which is specific for carrying aspartic acid to sites on the ribosomes in preparation for protein synthesis.
The region of an enzyme that interacts with its substrate to cause the enzymatic reaction.
Extrachromosomal, usually CIRCULAR DNA molecules that are self-replicating and transferable from one organism to another. They are found in a variety of bacterial, archaeal, fungal, algal, and plant species. They are used in GENETIC ENGINEERING as CLONING VECTORS.
The level of protein structure in which regular hydrogen-bond interactions within contiguous stretches of polypeptide chain give rise to alpha helices, beta strands (which align to form beta sheets) or other types of coils. This is the first folding level of protein conformation.
The sum of the weight of all the atoms in a molecule.
Process of generating a genetic MUTATION. It may occur spontaneously or be induced by MUTAGENS.
Enzymes that catalyze the transfer of hexose groups. EC 2.4.1.-.
Derivatives of GLUTAMIC ACID. Included under this heading are a broad variety of acid forms, salts, esters, and amides that contain the 2-aminopentanedioic acid structure.
Proteins found in any species of bacterium.
A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
Conjugated protein-carbohydrate compounds including mucins, mucoid, and amyloid glycoproteins.
Derivatives of acetic acid with one or more fluorines attached. They are almost odorless, difficult to detect chemically, and very stable. The acid itself, as well as the derivatives that are broken down in the body to the acid, are highly toxic substances, behaving as convulsant poisons with a delayed action. (From Miall's Dictionary of Chemistry, 5th ed)
An enzyme that catalyzes the transfer of methyl groups from S-adenosylmethionine to free carboxyl groups of a protein molecule forming methyl esters. EC 2.1.1.-.
A non-essential amino acid. It is found primarily in gelatin and silk fibroin and used therapeutically as a nutrient. It is also a fast inhibitory neurotransmitter.

Hemoglobin Providence. A human hemoglobin variant occurring in two forms in vivo. (1/1939)

Hemoglobin Providence Asn and Hemoglobin Providence Asp are two abnormal hemoglobins which apparently arise from a single genetic change that substitutes asparagine for lysine at position 82 (EF6) in the beta chain of human hemoglobin. The second form appears to be thr result of a partial in vivo deamidation of the asparagine situated at position beta 82. Cellulose acetate and citrate agar electrophoresis of hemolysates from patients with this abnormality shows three bands. Globin chain electrophoresis at acid and alkaline pH shows three beta chains. These three chains correspond to the normal beta A chain and two abnormal beta chains. Sequence analysis indicates that the two abnormal chains differ from beta A at only position beta 82. In the two abnormal chains, the residue which is normally lysine is substituted either by asparagine or by aspartic acid. These substitutions are notable because beta 82 lysine is one of the residues involved in 2,3-diphosphoglycerate binding. Additionally, beta 82 lysine is typically invariant in hemoglobin beta chain sequences. Sequence data on the two forms of Hemoglobin Providence are given in this paper. The functional properties of these two forms are described in the next paper.  (+info)

Merbarone, a catalytic inhibitor of DNA topoisomerase II, induces apoptosis in CEM cells through activation of ICE/CED-3-like protease. (2/1939)

Merbarone (5-[N-phenyl carboxamido]-2-thiobarbituric acid) is an anticancer drug that inhibits the catalytic activity of DNA topoisomerase II (topo II) without damaging DNA or stabilizing DNA-topo II cleavable complexes. Although the cytotoxicity of the complex-stabilizing DNA-topo II inhibitors such as VP-16 (etoposide) has been partially elucidated, the cytotoxicity of merbarone is poorly understood. Here, we report that merbarone induces programmed cell death or apoptosis in human leukemic CEM cells, characterized by internucleosomal DNA cleavage and nuclear condensation. Treatment of CEM cells with apoptosis-inducing concentrations of merbarone caused activation of c-Jun NH2-terminal kinase/stress-activated protein kinase, c-jun gene induction, activation of caspase-3/CPP32-like protease but not caspase-1, and the proteolytic cleavage of poly(ADP-ribose) polymerase. Treatment of CEM cells with a potent inhibitor of caspases, Z-Asp-2. 6-dichlorobenzoyloxymethyl-ketone, inhibited merbarone-induced caspase-3/CPP32-like activity and apoptosis in a dose-dependent manner. These results indicate that the catalytic inhibition of topo II by merbarone leads to apoptotic cell death through a caspase-3-like protease-dependent mechanism. These results further suggest that c-Jun and c-Jun NH2-terminal kinase/stress-activated protein kinase signaling may be involved in the cytotoxicity of merbarone.  (+info)

Distortion of the L-->M transition in the photocycle of the bacteriorhodopsin mutant D96N: a time-resolved step-scan FTIR investigation. (3/1939)

The D96N mutant of bacteriorhodopsin has often been taken as a model system to study the M intermediate of the wild type photocycle due to the long life time of the corresponding intermediate of the mutant. Using time-resolved step-scan FTIR spectroscopy in combination with a sample changing wheel we investigated the photocycle of the mutant with microsecond time resolution. Already after several microseconds an intermediate similar to the MN state is observed, which contrasts with the M state of the wild type protein. At reduced hydration M and N intermediates similar to those of wild type BR can be detected. These results have a bearing on the interpretation of the photocycle of this mutant. A mechanism is suggested for the fast rise of MN which provides some insight into the molecular events involved in triggering the opening of the cytosolic channel also of the wild type protein.  (+info)

Interaction of asparagine and EGF in the regulation of ornithine decarboxylase in IEC-6 cells. (4/1939)

Our laboratory has shown that asparagine (ASN) stimulates both ornithine decarboxylase (ODC) activity and gene expression in an intestinal epithelial cell line (IEC-6). The effect of ASN is specific, and other A- and N-system amino acids are almost as effective as ASN when added alone. In the present study, epidermal growth factor (EGF) was unable to increase ODC activity in cells maintained in a salt-glucose solution (Earle's balanced salt solution). However, the addition of ASN (10 mM) in the presence of EGF (30 ng/ml) increased the activity of ODC 0.5- to 4-fold over that stimulated by ASN alone. EGF also showed induction of ODC with glutamine and alpha-aminoisobutyric acid, but ODC induction was maximum with ASN and EGF. Thus the mechanism of the interaction between ASN and EGF is important for understanding the regulation of ODC under physiological conditions. Therefore, we examined the expression of the ODC gene and those for several protooncogenes under the same conditions. Increased expression of the genes for c-Jun and c-Fos but not for ODC occurred with EGF alone. The addition of ASN did not further increase the expression of the protooncogenes, but the combination of EGF and ASN further increased the expression of ODC over that of ASN alone. Western analysis showed no significant difference in the level of ODC protein in Earle's balanced salt solution, ASN, EGF, or EGF plus ASN. Addition of cycloheximide during ASN and ASN plus EGF treatment completely inhibited ODC activity without affecting the level of ODC protein. These results indicated that 1) the increased expression of protooncogenes in response to EGF is independent of increases in ODC activity and 2) potentiation between EGF and ASN on ODC activity may not be due to increased gene transcription but to posttranslational regulation and the requirement of ongoing protein synthesis involving a specific factor dependent on ASN.  (+info)

Glycosylation of asparagine-28 of recombinant staphylokinase with high-mannose-type oligosaccharides results in a protein with highly attenuated plasminogen activator activity. (5/1939)

The properties of recombinant staphylokinase (SakSTAR) expressed in Pichia pastoris cells have been determined. The single consensus N-linked oligosaccharide linkage site in SakSTAR (at Asn28 of the mature protein) was occupied in approximately 50% of the expressed protein with high-mannose-type oligosaccharides. The majority of these glycans ranged in polymerization state from Man8GlcNAc2 to Man14GlcNAc2, with the predominant species being Man10GlcNAc2 and Man11GlcNAc2. Glycosylated SakSTAR (SakSTARg) did not differ from its aglycosyl form in its aggregation state in solution, its thermal denaturation properties, its ability to form a complex with human plasmin (hPm), the amidolytic properties of the respective SakSTAR-hPm complexes, or its ability to liberate the amino-terminal decapeptide required for formation of a functional SakSTAR-hPm plasminogen activator complex. However, this latter complex with SakSTARg showed a greatly reduced ability to activate human plasminogen (hPg) as compared with the same complex with the aglycosyl form of SakSTAR. We conclude that glycosylation at Asn28 does not affect the structural properties of SakSTAR or its ability to participate in the formation of an active enzymatic complex with hPm, but it is detrimental to the ability of the SakSTAR-hPm complex to serve as a hPg activator. This is likely due to restricted access of hPg to the active site of the SakSTARg-hPm complex.  (+info)

The presence of pseudouridine in the anticodon alters the genetic code: a possible mechanism for assignment of the AAA lysine codon as asparagine in echinoderm mitochondria. (6/1939)

It has been inferred from DNA sequence analyses that in echinoderm mitochondria not only the usual asparagine codons AAU and AAC, but also the usual lysine codon AAA, are translated as asparagine by a single mitochondrial (mt) tRNAAsn with the anticodon GUU. Nucleotide sequencing of starfish mt tRNAAsn revealed that the anticodon is GPsiU, U35 at the anticodon second position being modified to pseudouridine (Psi). In contrast, mt tRNALys, corresponding to another lysine codon, AAG, has the anticodon CUU. mt tRNAs possessing anti-codons closely related to that of tRNAAsn, but responsible for decoding only two codons each-tRNAHis, tRNAAsp and tRNATyr-were found to possess unmodified U35 in all cases, suggesting the importance of Psi35 for decoding the three codons. Therefore, the decoding capabilities of two synthetic Escherichia coli tRNAAla variants with the anticodon GPsiU or GUU were examined using an E.coli in vitro translation system. Both tRNAs could translate not only AAC and AAU with similar efficiency, but also AAA with an efficiency that was approximately 2-fold higher in the case of tRNAAlaGPsiU than tRNAAlaGUU. These findings imply that Psi35 of echinoderm mt tRNAAsn actually serves to decode the unusual asparagine codon AAA, resulting in the alteration of the genetic code in echinoderm mitochondria.  (+info)

L-Asparagine synthetase in serum as a marker for neoplasia. (7/1939)

L-Asparagine synthetase appears in serum approximately 7 days after the s.c. implantation of 1 X 10(5) cells of Leukemia 5178Y/AR (resistant to L-asparaginase) and increases in activity as the neoplasm grows and metastasizes. The principal source of the enzyme is the primary tumor. After intravranial inoculation of tumor, the rate of leakage of the enzyme is more pronounced than when the subcutaneous, intramuscular, or intraperitoneal routes are used. 1-(2-Chloroethyl)-3-cyclohexyl-1-nitrosourea (NSC 79037), a nitro-sourea effective in the palliation of L5178Y/AR, temporarily halts the influx of enzyme into the blood stream, as does surgical excision of the s.c. tumor nodules. Treatment of mice with L-asparaginase within 24 hr of inoculation of the tumor markedly augments both tumor growth and the rate of penetration of L-asparagine synthetase into the circulation. Several other L-asparagine synthetase into the circulation. Several other L-asparaginase-resistant tumors also were found to spill L-asparagine synthetase into the serum, but the correlation between this phenomenon and the specific activity of the enzyme in homogenates of the tumor was imperfect.  (+info)

Conserved polar residues in the transmembrane domain of the human tachykinin NK2 receptor: functional roles and structural implications. (8/1939)

We have studied the effects of agonist and antagonist binding, agonist-induced activation and agonist-induced desensitization of the human tachykinin NK2 receptor mutated at polar residues Asn-51 [in transmembrane helix 1 (TM1)], Asp-79 (TM2) and Asn-303 (TM7), which are highly conserved in the transmembrane domain in the rhodopsin family of G-protein-coupled receptors. Wild-type and mutant receptors were expressed in both COS-1 cells and Xenopus oocytes. The results show that the N51D mutation results in a receptor which, in contrast with the wild-type receptor, is desensitized by the application of a concentration of 1 microM of the partial agonist GR64349, indicating that the mutant is more sensitive to agonist activation than is the wild-type receptor. In addition, we show that, whereas the D79E mutant displayed activation properties similar to those of the wild-type receptor, the D79N and D79A mutants displayed a severely impaired ability to activate the calcium-dependent chloride current. This suggests that it is the negative charge at Asn-79, rather than the ability of this residue to hydrogen-bond, that is critical for the activity of the receptor. Interestingly, the placement of a negative charge at position 303 could compensate for the removal of the negative charge at position 79, since the double mutant D79N/N303D displayed activation properties similar to those of the wild-type receptor. This suggests that these two residues are functionally coupled, and may even be in close proximity in the three-dimensional structure of the human tachykinin NK2 receptor. A three-dimensional model of the receptor displaying this putative interaction is presented.  (+info)

Bovine prothrombin contains three asparagine-linked sugar chains in 1 molecule. The sugar chains were quantitatively released from the polypeptide backbone by hydrazinolysis. All of the oligosaccharides thus obtained contain N-acetylneuraminic acid.
We have derived a novel method to assess compositional biases in biological sequences, which is based on finding the lowest-probability subsequences for a given residue-type set. As a case study, the distribution of prion-like glutamine/asparagine-rich ((Q+N)-rich) domains (which are linked to amyloidogenesis) was assessed for budding and fission yeasts and four other eukaryotes. We find more than 170 prion-like (Q+N)-rich regions in budding yeast, and, strikingly, many fewer in fission yeast. Also, some residues, such as tryptophan or isoleucine, are unlikely to form biased regions in any eukaryotic proteome.
A variety of unconventional translational and posttranslational mechanisms contribute to the production of antigenic peptides, thereby increasing the diversity of the peptide repertoire presented by MHC class I molecules. Here, we describe a class I-restricted peptide that combines several posttranslational modifications. It is derived from tyrosinase and recognized by tumor-infiltrating lymphocytes isolated from a melanoma patient. This unusual antigenic peptide is made of two noncontiguous tyrosinase fragments that are spliced together in the reverse order. In addition, it contains two aspartate residues that replace the asparagines encoded in the tyrosinase sequence. We confirmed that this peptide is naturally presented at the surface of melanoma cells, and we showed that its processing sequentially requires translation of tyrosinase into the endoplasmic reticulum and its retrotranslocation into the cytosol, where deglycosylation of the two asparagines by peptide-N-glycanase turns them into
Translations: Asparagīna Amino Acid, Asparaginas aminorūgšties, Asparagina aminoacizi, Asparagin Aminokiselinska, Amino Acid Asparagine, Asparaginy aminokwasów, Asparagine एमिनो एसिड, Aminoácido asparagina, Аспарагин Аминокислоты, Ασπαραγίνη Αμινοξύ, الهليونين الأحماض الأمينية, 아스파라긴 아미노산, Asparagin aminokyselin, Asparagina Asam Amino, Asparagine Amino acid, 天冬酰胺氨基酸, Asparagina Aminoàcids, Asparagin Amino Acid, Asparagín aminokyselín, Amminoacido asparagina, אספרגין חומצה אמינו, Asparagin Amino Acid, Аспарагин амино киселина, アスパラギンアミノ酸, Acide aminé asparagine, Asparagin Amino Acid, Asparagin Amino Acid, Asparaginer Amino Acid, Asparagina Aminoácidos, Аспарагін Амінокислоти, Asparagiini Aminohappo, Аспарагин амино ...
The structure of synC can be divided into three subdomains (Figure 1D): the amino‐terminal subdomain (residues 110‐223), the central subdomain (residues 246‐308) and the carboxy‐terminal subdomain (residues 224‐245 and 309‐420). The core of the amino‐terminal subdomain is a four‐stranded parallel β‐sheet (β1, β2, β6, β7), which is flanked by a helical loop (residues 124‐137) and helix α1. It resembles the nucleotide‐binding motif (NAD motif) found in numerous enzymes that bind substrates at the carboxyl end of the parallel β‐sheet. The parallel arrangement of helices α1 and α2 and their connection by strand β7 are remarkably well conserved in synC and GSHase. Even more remarkable is the existence of a cis‐asparagine residue at the carboxyl end of strand β7 in both synC (Asn214) and GSHase (Asn114). As the cis conformation is extremely rare in peptide bonds preceding residues other than proline, the use of cis‐asparagine at equivalent positions in synC and ...
Although bafilomycin induced HIF-1α levels under normoxic conditions, it has little effect on the expressions of HIF-1 targeted genes. This effect of bafilomycin on HIF-1α could be suspected of the factor-inhibiting HIF (FIH). In the absence of a hypoxic signal, HIF-1α can be inactivated by FIH. FIH hydroxylates an asparagine residue (Asn803) within the transactivation domain of HIF-1α, which blocks its recruitment of p300 coactivator (Lando et al., 2002). Moreover, under hypoxic conditions, asparagine hydroxylation is inhibited due to limited oxygen, and HIF-1α remains unmodified and activated. This seems to be one of the reasons why HIF-1α induced by bafilomycin has little transcriptional activity; similarly, HIF-1α induced by heat shock was found to have no transcriptional activity (Katschinski et al., 2002). However, HIF-1α induced by bafilomycin induced p21 transcription. Recently, Koshiji et al. (2004) demonstrated the mechanism of p21 induction by HIF-1α (i.e., c-Myc represses ...
The amino acid asparagine was until now considered non-essential because it is produced naturally by the body. However, researchers found that it is essential for normal brain development.
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The researchers narrow it down to a single change in the outer coat of the virus. S139N - the switch in amino acids from serine to asparagine at position 139 in the membrane protein (PrM). This change was sufficient to help Zika virus infect brain cells from both humans and mice efficiently. Contributing to an unprecedented outbreak.. Reference. 1. A single mutation in the prM protein of Zika virus contributes to fetal microcephaly.Yuan L, Huang XY, Liu ZY, Zhang F, Zhu XL, Yu JY, Ji X, Xu YP, Li G, Li C, Wang HJ, Deng YQ, Wu M, Cheng ML, Ye Q, Xie DY, Li XF, Wang X, Shi W, Hu B, Shi PY, Xu Z, Qin CF. Science. 2017 Sep 28. pii: eaam7120. doi: 10.1126/science.aam7120.. ...
This sequence change replaces histidine with asparagine at codon 6717 of the SYNE1 protein (p.His6717Asn). The histidine residue is highly conserved and there is a small physicochemical difference between histidine and asparagine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with SYNE1-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be disruptive, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance ...
Alg6 - Alg6 (untagged ORF) - Rat asparagine-linked glycosylation 6, alpha-1,3-glucosyltransferase homolog (S. cerevisiae) (Alg6), (10 ug) available for purchase from OriGene - Your Gene Company.
Asparagine is an amino acid, which has recently been rumored to aid the spread of breast cancer. Trials on mice have shown that low-asparagine diets, combined with blocking asparagine production in the body, greatly reduced the breast cancers ability to spread.. ...
This gene encodes an enzyme that catalyzes hydrolysis of an N(4)-(acetyl-beta-D-glucosaminyl) asparagine residue to N-acetyl-beta-D-glucosaminylamine and a peptide containing an aspartate residue. The encoded enzyme may play a role in the proteasome-mediated degradation of misfolded glycoproteins. Multiple transcript variants encoding different isoforms have been found for this gene ...
Looking for online definition of Asparagine-linked glycosylation protein 6 homolog in the Medical Dictionary? Asparagine-linked glycosylation protein 6 homolog explanation free. What is Asparagine-linked glycosylation protein 6 homolog? Meaning of Asparagine-linked glycosylation protein 6 homolog medical term. What does Asparagine-linked glycosylation protein 6 homolog mean?
The asparaginyl hydroxylase FIH [factor inhibiting HIF (hypoxia-inducible factor)] was first identified as a protein that inhibits transcriptional activation by HIF, through hydroxylation of an asparagine residue in the CAD (C-terminal activation domain). More recently, several ARD [AR (ankyrin repeat) domain]-containing proteins were identified as FIH substrates using FIH interaction assays. Although the function(s) of these ARD hydroxylations is unclear, expression of the ARD protein Notch1 was shown to compete efficiently with HIF CAD for asparagine hydroxylation and thus to enhance HIF activity. The ARD is a common protein domain with over 300 examples in the human proteome. However, the extent of hydroxylation among ARD proteins, and the ability of other members to compete with HIF-CAD for FIH, is not known. In the present study we assay for asparagine hydroxylation in a bioinformatically predicted FIH substrate, the targeting subunit of myosin phosphatase, MYPT1. Our results confirm hydroxylation
Activity of the hypoxia-inducible factor (HIF) complex is controlled by oxygen-dependent hydroxylation of prolyl and asparaginyl residues. Hydroxylation of specific prolyl residues by 2-oxoglutarate (2-OG)-dependent oxygenases mediates ubiquitinylation and proteasomal destruction of HIF-alpha. Hydroxylation of an asparagine residue in the C-terminal transactivation domain (CAD) of HIF-alpha abrogates interaction with p300, preventing transcriptional activation. Yeast two-hybrid assays recently identified factor inhibiting HIF (FIH) as a protein that associates with the CAD region of HIF-alpha. Since FIH contains certain motifs present in iron- and 2-OG-dependent oxygenases we investigated whether FIH was the HIF asparaginyl hydroxylase. Assays using recombinant FIH and HIF-alpha fragments revealed that FIH is the enzyme that hydroxylates the CAD asparagine residue, that the activity is directly inhibited by cobalt(II) and limited by hypoxia, and that the oxygen in the alcohol of the hydroxyasparagine
Asparagine (Asn) is one of the 20 most common natural amino acids on Earth. It has carboxamide as the side chains functional group. Asparagine is not an essential amino acid, which means that it can be synthesized from central metabolic pathway intermediates in humans and is not required in the diet. The precursor to asparagine is oxaloacetate. Oxaloacetate is converted to aspartate using a transaminase enzyme. The enzyme transfers the amino group from glutamate to oxaloacetate producing alpha-ketoglutarate and aspartate. The enzyme asparagine synthetase produces asparagine, AMP, glutamate, and pyrophosphate from aspartate, glutamine, and ATP. In the asparagine synthetase reaction, ATP is used to activate aspartate, forming beta-aspartyl-AMP. Glutamine donates an ammonium group which reacts with beta-aspartyl-AMP to form asparagine and free AMP. Since the asparagine side chain can make efficient hydrogen bond interactions with the peptide backbone, asparagines are often found near the beginning ...
Background Polyglutamine expansion is responsible for several neurodegenerative disorders, among which Huntington disease is the most well-known. Studies in the yeast model demonstrated that both aggregation and toxicity of a huntingtin (htt) protein with an expanded polyglutamine region strictly depend on the presence of the prion form of Rnq1 protein ([PIN+]), which has a glutamine/asparagine-rich domain. Principal Findings Here, we showed that aggregation and toxicity of mutant htt depended on [PIN+] only quantitatively: the presence of [PIN+] elevated the toxicity and the levels of htt detergent-insoluble polymers. In cells lacking [PIN+], toxicity of mutant htt was due to the polymerization and inactivation of the essential glutamine/asparagine-rich Sup35 protein and related inactivation of another essential protein, Sup45, most probably via its sequestration into Sup35 aggregates. However, inhibition of growth of [PIN+] cells depended on Sup35/Sup45 depletion only partially, suggesting that
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Asparagine. Molecular model of the amino acid asparagine. Its chemical formula is C4.H8.N2.O3. Atoms are represented as spheres and are colour- coded: carbon (blue), hydrogen (gold), oxygen (red) and nitrogen (dark blue). Amino acids are the building blocks of proteins. Asparagine is a non-essential amino acid. It can be synthesised by the body and so does not need to come from the diet. Asparagine plays an important role in the folding of protein molecules into their secondary structures (alpha helices and beta sheets). Some proteins (such as haemoglobin, the oxygen- carrying pigment in human blood) cannot function without being folded into the correct shape. - Stock Image A611/0042
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Asparagine-linked sugar chains of glycoproteins in calf thymocyte plasma membrane. Isolation and fractionation of oligosaccharides liberated by hydrazinolysis.:Isolation and Fractionation of Oligosaccharides Liberated by Hydrazinolysis (1980 ...
The mechanism by which asparaginase inhibits the 6C3HED tumor is probably not directly related to the cellular concentration of asparagine, since the concentration of asparagine decreases in resistant tumors, spleen, and liver, as well as in susceptible tumors. Amino acids other than asparagine may be affected by asparaginase because of the variety of metabolic relationships of the amino acids. In this study, analyses of all the amino acids of resistant 6C3HED tumor, susceptible 6C3HED tumor, spleen, and liver were undertaken.. Most of the amino acids of the susceptible tumor increased from 2- to 40-fold, while only slight changes occurred in the resistant tumor. The most dramatic change was a decrease in glycine in the susceptible tumor. No parallel change in glycine occurred in the resistant tumor, the spleen, or the liver. It is suggested that the susceptible tumor may synthesize glycine from asparagine; consequently, the decrease in asparagine is followed by a decrease in cellular glycine. ...
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The researchers narrow it down to a single change in the outer coat of the virus. S139N - the switch in amino acids from serine to asparagine at position 139 in the membrane protein (PrM). This change was sufficient to help Zika virus infect brain cells from both humans and mice efficiently. Contributing to an unprecedented outbreak.. Reference. 1. A single mutation in the prM protein of Zika virus contributes to fetal microcephaly.Yuan L, Huang XY, Liu ZY, Zhang F, Zhu XL, Yu JY, Ji X, Xu YP, Li G, Li C, Wang HJ, Deng YQ, Wu M, Cheng ML, Ye Q, Xie DY, Li XF, Wang X, Shi W, Hu B, Shi PY, Xu Z, Qin CF. Science. 2017 Sep 28. pii: eaam7120. doi: 10.1126/science.aam7120.. ...
Most core residues of coiled coils are hydrophobic. Occasional polar residues are thought to lower stability, but impart structural specificity. The coiled coils of trimeric autotransporter adhesins (TAAs) are conspicuous for their large number of polar residues in position d of the core, which often leads to their prediction as natively unstructured regions. The most frequent residue, asparagine ([email protected]), can occur in runs of up to 19 consecutive heptads, frequently in the motif [I/V]xxNTxx. In the Salmonella TAA, SadA, the core asparagines form rings of interacting residues with the following threonines, grouped around a central anion. This conformation is observed generally in [email protected] layers from trimeric coiled coils of known structure. Attempts to impose a different register on the motif show that the asparagines orient themselves specifically into the core, even against conflicting information from flanking domains. When engineered into the GCN4 leucine zipper, [email protected] layers progressively ...
Product Number , 75190706. CAS Number , 5794-24-1. EC , 218-163-3. Molecular Formula , C4H8N2O3Ï H2O. Molecular Weight , 150.14. Storage Temp , +20°C. Harmonized Tariff code , 29241900900. Signal Word , ...
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BioAssay record AID 253508 submitted by ChEMBL: Concentration of compound inhibiting Lys103-Asn mutant HIV-1(IIIB) induced cytopathicity in CEM cell culture by 50%.
Research into the chemical biology of bromodomains has been driven by the development of acetyl-lysine mimetics. The ligands are typically anchored by binding to a highly conserved asparagine residue. Atypical bromodomains, for which the asparagine is mutated, have thus far proven elusive targets, including
Zotik an jî anûs di anatomî de ew qulika dervayî ji rektum (ji latînî hatiye, ango rast). Zotik beşeke navende di qûnê mirov de û beşa dawî ji sîstema givêrdarê (hezmê) de ku mayînên laşê wek gû (feces bi Înglîzî) ji têne avêtin ku ji bi Înglîzî defaction tê gotin, û ev jî erkeke bingeh û gelek pêwîste ji erkên (fanksiyonên) zûtik û qûn di laşê mirov de. Zotik roleke di zayenditî de dilîze di kirdarê anal seks ango kirdarê zayendî bi riya qûn yan qûnetî (lotî) ku li pir civaktiyên wek civaktiyên misilmana gune ye û dijî olê Îslamê ye. Bi riya zûtik çend înfeksiyonan peyda dibe wek şêrpençîr (cancer). Bo tendirustiya zûtik û qûn pakî (paqijî) divê bi av û sabûn pey destavê û di serşûştinê ne bi pelê tuwelêtê ku baş paqij nake. ...
Aspartate-Ammonia Ligase: An enzyme that catalyzes the formation of asparagine from ammonia and aspartic acid, in the presence of ATP. EC 6.3.1.1.
அஸ்பரஜின் (Asparagine) (அ) அஸ்பரமைடு [குறுக்கம்: Asn (அ) N; அஸ்பார்டிக் அமிலம் (அ) அஸ்பரஜின் அமினோ அமிலத்தை குறிக்கும் மற்றொரு குறுக்கம்: Asx or B][2] புரதங்களில் அடிப்படையாக உள்ள 20 அமினோ அமிலங்களில் ஒன்றாகும். இதனுடைய வாய்பாடு: 2HN-CO-CH2-CH(NH2)-COOH (அ) C4H8N2O3. இது ஒரு அத்தியாவசியமற்ற ஆல்ஃபா அமினோ அமிலமாகும். அஸ்பரஜின் விலங்குகளினால்/மனிதர்களால் தயாரிக்கப்படக்கூடியது. இதன் குறிமுறையன்கள்: AAU மற்றும் AAC. ...
Hydrolysis of an N(4)-(acetyl-beta-D- glucosaminyl)asparagine residue in which the glucosamine residue may be further glycosylated, to yield a (substituted) N-acetyl- beta-D-glucosaminylamine and a peptide containing an aspartate residue ...
1NJE: Partitioning roles of side chains in affinity, orientation, and catalysis with structures for mutant complexes: asparagine-229 in thymidylate synthase.
1NJB: Partitioning roles of side chains in affinity, orientation, and catalysis with structures for mutant complexes: asparagine-229 in thymidylate synthase.
II. LYMPHOMA 6C3HED CELLS CULTURED IN A MEDIUM DEVOID OF L-ASPARAGINE LOSE THEIR SUSCEPTIBILITY TO THE EFFECTS OF GUINEA PIG SERUM IN VIVO ...
Po e ndjekim hap pas hapi ecurinë e analizës së këtij shkruesi që lodhet shumë pa e ditur mirë se çfarë po shkruan, meqë ende nuk i ka fituar aftësitë e mundësitë e duhura me atë përvojë të pakët profesionale në fushën e letërsisë shqipe, e cila është një shkencë serioze dhe me kontribute të lashta sasiore e cilësore. Mbasi vlerat e saja estetiko-artistike janë të njohura me kohë kombëtarisht e botërisht. Le tua lëmë fjalën pjesëve problematike e thelbësore të këtij shkrimi. Shkruesi që në fillim arsyeton, me një analizë jo të thelluar dhe mjaft sipërfaqësore e hera-herës me një kuptim të kundërt me çfarë kumton përmbajtja e poezive të këtij autori, duke e krahasuar përmbajtjen e tyre me disa fjalë të huaja. Konkretisht ai shprehet:Ditarët e mjegullës, një metaforë që në profecinë e saj paralajmëron...ngulmimet e poetit...në imazherinë e shoqërisë e të hapë rrugëkalimet drejt një prosperiteti të dëshirueshëm nën ...
IKSHP tregon si nevojitet të sillemi gjatë festës së Kurban Bajramit - IKSHPK ka udhëzuar qytetarët që në vend se të bëni një udhëtim, qëndroni të lidhur me
Complete Information about ASN 131258 including Assigned Organization, IP range count, and Country range count. Research all IP ranges within ASN 131258 including specific CIDR data, Subnets, and IP address location information.
سیانوباکترها یک گروه منحصر به فرد از باکتری-های فتواتوتروف هستند که برخی از آن‌ها به دلیل ویژگی-های ساختاری، تحمل قابل توجهی به تنش شوری نشان می-دهند. این موجودات نقش مهمی در محیط-های خاکی به ویژه در نواحی خشک و نیمه-خشک ایفا می-کنند. در مطالعه حاضر سیانوباکترهای خاک از مناطق بیابانی ایران جداسازی شده و سپس جدایه-های مقاوم به شرایط فوق شور شناسایی شدند. 40 نمونه خاک از پارک ملی کویر تهیه شد. نمونه-ها پس از کشت در محیط BG11 و ASN III (5/3، 5، 6 و 7 درصد کلرید سدیم) و انکوباسیون در شرایط مناسب دمایی و نور، جداسازی شده و با استفاده از کلیدهای مورفولوژیکی به طور اولیه و سپس با
TY - JOUR. T1 - Amino Acid Templating of Inorganic Networks. T2 - Synthesis and Structure of L-Asparagine Zinc Phosphite, C4N2O3H 8·ZnHPO3. AU - Gordon, Laura E.. AU - Harrison, William T.A.. PY - 2004/3/22. Y1 - 2004/3/22. N2 - C4N2O3H8·ZnHPO 3 is the first zincophosphite framework to be templated by an amino acid (L-asparagine), which bonds to Zn via a carboxyl O atom. It contains infinite, homochiral, helical 4-ring chains of ZnO4 and HPO 3 groups, stabilized by intra- and interchain N-H⋯O hydrogen bonds. Crystal data: C4N2O3H 8·ZnHPO3, Mr = 277.49, orthorhombic, P212121 (No. 19), a = 5.0349(2) Å, b = 9.4539(4) Å, c = 18.6092(8) Å, V = 885,79 (6) Å3, Z = 4.. AB - C4N2O3H8·ZnHPO 3 is the first zincophosphite framework to be templated by an amino acid (L-asparagine), which bonds to Zn via a carboxyl O atom. It contains infinite, homochiral, helical 4-ring chains of ZnO4 and HPO 3 groups, stabilized by intra- and interchain N-H⋯O hydrogen bonds. Crystal data: C4N2O3H 8·ZnHPO3, Mr = ...
The antileukemic activity of l-asparaginase (ASNase), an important component of therapy for acute lymphoblastic leukemia, is thought to result from depletion of serum l-asparagine (Asn). In studies of the pharmacological effects of ASNase, investigators have reported prolonged reduction in the serum concentration of Asn after the administration of ASNase. Such measurements may not be valid because ASNase present in the blood sample may hydrolyze Asn before its determination. We examined recovery of [U-14C]Asn from blood samples with and without various concentrations of added ASNase. In the presence of ≥0.01 IU/ml of ASNase, the amount of [U-14C]Asn recovered was ,15% of that without ASNase. Utilizing this assay, we studied the effect of 2 known inhibitors of ASNase in an attempt to improve Asn recovery. In the presence of aspartic β semialdehyde (ASA), or 5-diazo-4-oxo-l-norvaline (DONV), and up to 1.0 IU/ml ASNase, Asn levels remained at ,90% of control. ASA prevented the hydrolysis of ...
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Targeting amino acid metabolism has therapeutic implications for aggressive brain tumors. Asparagine is an amino acid that is synthesized by normal cells. However, some cancer cells lack asparagine synthetase (ASNS), the key enzyme for asparagine synthesis. Asparaginase (ASNase) contributes to eradication of acute leukemia by decreasing asparagine levels in serum and cerebrospinal fluid. However, leukemic cells may become ASNase-resistant by up-regulating ASNS. High expression of ASNS has also been associated with biological aggressiveness of other cancers, including gliomas. Here, the impact of enzymatic depletion of asparagine on proliferation of brain tumor cells was determined. ASNase was used as monotherapy or in combination with conventional chemotherapeutic agents. Viability assays for ASNase-treated cells demonstrated significant growth reduction in multiple cell lines. This effect was reversed by glutamine in a dose-dependent manner -- as expected, because glutamine is the main amino ...
Sugar moieties on the cell surface play one of the most important roles in cellular recognition. In order to elucidate the molecular mechanism of these cellular phenomena, assessment of the structure...
A sequence of about forty amino-acid residues found in epidermal growth factor (EGF) has been shown [ (PUBMED:2288911) (PUBMED:6334307) (PUBMED:3534958) (PUBMED:6607417) (PUBMED:3282918) ] to be present in a large number of membrane-bound and extracellular, mostly animal, proteins. Many of these proteins require calcium for their biological function and a calcium-binding site has been found at the N terminus of some EGF-like domains [ (PUBMED:1527084) ]. Calcium-binding may be crucial for numerous protein-protein interactions. For human coagulation factor IX it has been shown [ (PUBMED:7606779) ] that the calcium-ligands form a pentagonal bipyramid. The first, third and fourth conserved negatively charged or polar residues are side chain ligands. The latter is possibly hydroxylated (see aspartic acid and asparagine hydroxylation site) [ (PUBMED:1527084) ]. A conserved aromatic residue, as well as the second conserved negative residue, are thought to be involved in stabilising the calcium-binding ...
A sequence of about forty amino-acid residues found in epidermal growth factor (EGF) has been shown [ (PUBMED:2288911) (PUBMED:6334307) (PUBMED:3534958) (PUBMED:6607417) (PUBMED:3282918) ] to be present in a large number of membrane-bound and extracellular, mostly animal, proteins. Many of these proteins require calcium for their biological function and a calcium-binding site has been found at the N terminus of some EGF-like domains [ (PUBMED:1527084) ]. Calcium-binding may be crucial for numerous protein-protein interactions. For human coagulation factor IX it has been shown [ (PUBMED:7606779) ] that the calcium-ligands form a pentagonal bipyramid. The first, third and fourth conserved negatively charged or polar residues are side chain ligands. The latter is possibly hydroxylated (see aspartic acid and asparagine hydroxylation site) [ (PUBMED:1527084) ]. A conserved aromatic residue, as well as the second conserved negative residue, are thought to be involved in stabilising the calcium-binding ...
HIF plays a central role in the transcriptional response to changes in oxygen availability. The PHD family of oxygen-dependent prolyl hydroxylases plays a pivotal role in regulating HIF stability. The biochemical properties of these enzymes make them well suited to act as oxygen sensors. They also respond to other intracellular signals, including reactive oxygen species, nitric oxide, and certain metabolites, that can modulate the hypoxic response. HIF transcriptional activity is further tuned by FIH1-mediated asparagine hydroxylation. HIF affects signaling pathways that influence development, metabolism, inflammation, and integrative physiology. Accordingly, HIF-modulatory drugs are now being developed for diverse diseases.
Larsen TM, Boehlein SK, Schuster SM, Richards NG, Thoden JB, Holden HM, Rayment I (December 1999). Three-dimensional structure of Escherichia coli asparagine synthetase B: a short journey from substrate to product. Biochemistry. 38 (49): 16146-57. CiteSeerX 10.1.1.453.5998. doi:10.1021/bi9915768. PMID 10587437 ...
Suolinna, E; Tritsch, G; and Hakala, M T., Asparagine (asn) and glutamine (gln) metabolism in sarcoma 180 cells in vitro. Abstr. (1971). Subject Strain Bibliography 1971. 2397 ...
Asparagine is a nonessential amino acid, which means that it is manufactured from other amino acids in the liver; it does not have to be obtained directly through the diet.
Asparagine (abbreviated as Asn or N; Asx or B represent either asparagine or aspartic acid) is one of the 20 most common natural amino acids on Earth. It has carboxamide as the side chains functional group. It is not an essential amino acid. Its codons are AAU and AAC. A reaction between asparagine and reducing sugars or reactive carbonyls produces acrylamide (acrylic amide) in food when heated to sufficient temperature. These products occur in baked goods such as french fries, potato chips, and roasted coffee.
Asparagine synthetase antibody (asparagine synthetase (glutamine-hydrolyzing)) for IHC-P, WB. Anti-Asparagine synthetase pAb (GTX114269) is tested in Human samples. 100% Ab-Assurance.
p>The checksum is a form of redundancy check that is calculated from the sequence. It is useful for tracking sequence updates.,/p> ,p>It should be noted that while, in theory, two different sequences could have the same checksum value, the likelihood that this would happen is extremely low.,/p> ,p>However UniProtKB may contain entries with identical sequences in case of multiple genes (paralogs).,/p> ,p>The checksum is computed as the sequence 64-bit Cyclic Redundancy Check value (CRC64) using the generator polynomial: x,sup>64,/sup> + x,sup>4,/sup> + x,sup>3,/sup> + x + 1. The algorithm is described in the ISO 3309 standard. ,/p> ,p class=publication>Press W.H., Flannery B.P., Teukolsky S.A. and Vetterling W.T.,br /> ,strong>Cyclic redundancy and other checksums,/strong>,br /> ,a href=http://www.nrbook.com/b/bookcpdf.php>Numerical recipes in C 2nd ed., pp896-902, Cambridge University Press (1993),/a>),/p> Checksum:i ...
Background Voltage-dependent block from the NMDA receptor by Mg2+ is usually thought to be central to the unique involvement of this receptor in higher brain functions. hippocampal spatial info processing by attenuating activity-dependent synaptic potentiation in the dentate gyrus. overexpressing an NMDAR defective for Mg2+ block has problems in long-term memory space [7]. However, the role of the Mg2+ block in vertebrates still remains unclear. NMDARs defective for the Mg2+ block cause perinatal lethality in mice expressing these receptors [8]. A single amino acid substitution is known to greatly switch the Mg2+ blockade of the NMDAR. Practical NMDARs are likely hetero-oligomers comprising two types of subunits, GluN1 and GluN2. Each subunit offers four expected membrane-associated segments (M1CM4). A single asparagine residue in M2 is critical for voltage-dependent Mg2+ blockade. Alternative of asparagine 598 of the GluN1 subunit with glutamine strongly reduces the level of sensitivity of the ...
Alpha-1,2-mannosyltransferase, catalyzes sequential addition of the two terminal alpha 1,2-mannose residues to the Man5GlcNAc2-PP-dolichol intermediate during asparagine-linked glycosylation in the ...
Alg1 - Alg1 (untagged) - Mouse asparagine-linked glycosylation 1 homolog (yeast, beta-1,4-mannosyltransferase) (cDNA clone MGC:18946, (10ug) available for purchase from OriGene - Your Gene Company.
Lentivirus with CMV promoter-driven expression of asparagine-linked glycosylation 9, alpha-1,2-mannosyltransferase homolog (S. cerevisiae) (ALG9), transcript variant 1 in pLenti vector with puromycin selection and C-terminal Myc and FLAG tags.
Complete information for ASNS gene (Protein Coding), Asparagine Synthetase (Glutamine-Hydrolyzing), including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium
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Acts only on asparagine-oligosaccharides containing one amino acid, i.e., the asparagine has free alpha-amino and alpha-carboxyl groups [cf. EC 3.5.1.52, peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase ...
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Creative Biolabs has established a platform predict and assess deamidation of antibody therapeutics as part of manufacturability assessment.
ASN1_STRING_new() returns an allocated ASN1_STRING structure. Its type is undefined. ASN1_STRING_type_new() returns an allocated ASN1_STRING structure of type type. ASN1_STRING_free() frees up a. ...
Asparaginasefrom Escherichia coliL-Asparagine amidohydrolaseEC # 3.5.1.1If you need bigger quantities than indicated on the web site, please contact us for a personal offer.
Other names in common use include asparagine synthetase (ADP-forming), and asparagine synthetase (adenosine diphosphate-forming ... Nair PM (September 1969). "Asparagine synthetase from gamma-irradiated potatoes". Archives of Biochemistry and Biophysics. 133 ... L-asparagine The 3 substrates of this enzyme are ATP, L-aspartate, and NH3, whereas its 3 products are ADP, phosphate, and L- ... asparagine. This enzyme belongs to the family of ligases, specifically those forming carbon-nitrogen bonds as acid-D-ammonia ( ...
... on the interior and asparagine (R), Serine (and lysine (K) on the exterior. Asparagine residues may serve as an important ... Kornfeld, R.; Kornfeld, S. (1985). "Assembly of asparagine-linked oligosaccharides" (PDF). Annual Review of Biochemistry. 54: ...
"Entrez Gene: asparagine-linked glycosylation 11". Cipollo, JF; Trimble, RB; Chi, JH; Yan, Q; Dean, N (2001). "The yeast ALG11 ... Asparagine-linked glycosylation protein 11 is an enzyme encoded by the ALG11 gene. Congenital disorder of glycosylation GRCh38 ...
The difucosylation of asparagine-bound N-acetylglucosamine". Eur. J. Biochem. 199 (3): 745-51. doi:10.1111/j.1432-1033.1991. ... The systematic name of this enzyme class is GDP-L-fucose:glycoprotein (L-fucose to asparagine-linked N-acetylglucosamine of N4 ... asparagine The 5 substrates of this enzyme are GDP-L-fucose, [[N4-{N-acetyl-beta-D-glucosaminyl-(1->2)-alpha-D-mannosyl-(1->3 ... asparagine) 3-alpha-L-fucosyl-transferase. Other names in common use include GDP-L-Fuc:N-acetyl-beta-D-glucosaminide alpha1,3- ...
It has fewer aspartate, glutamate, and asparagine. The high ratio of basic to acidic amino acids contributes to the protein's ...
This amino acid was replaced with asparagine. The complication with mutations in the BCKDHA gene is that it disrupts the normal ...
Inhibition of L-'asparagine synthetase in vivo". Biochemical Pharmacology. 25 (16): 1851-8. doi:10.1016/0006-2952(76)90189-1. ... "Reactions of Pseudomonas 7A glutaminase-asparaginase with diazo analogues of glutamine and asparagine result in unexpected ...
Role of histidine 191 and asparagine 194". The Journal of Biological Chemistry. 273 (49): 32753-32762. doi:10.1074/jbc.273.49. ...
Ambasta RK, Ai X, Emerson CP (November 2007). "Quail Sulf1 function requires asparagine-linked glycosylation". The Journal of ...
Other names in common use include asparagine synthetase, and L-asparagine synthetase. This enzyme participates in 3 metabolic ... "Asparagine biosynthesis in Lactobacillus arabinosus and its control by asparagine through enzyme inhibition and repression". J ... Webster GC, Varner JE (1955). "Aspartate metabolism and asparagine synthesis in plant systems". J. Biol. Chem. 215: 91-99. PMID ... L-asparagine The 3 substrates of this enzyme are ATP, L-aspartate, and NH3, whereas its 3 products are AMP, diphosphate, and L- ...
Asparagine and aspartic acid are both larger than threonine, and both asparagine and aspartic acid like to be in a turn while ... Aspartic acid and asparagine carry a formal charge. This charge however is negative for aspartic acid and positive for ... Asparagine and aspartic acid are both hydrophilic, while threonine has intermediate hydrophilicity. ... asparagine. Phoratoxin has not been synthesized in a lab yet. It can, however, be extracted from the Phoradendron. Phoratoxin ...
50 mg each asparagine, cystine, leucine, and isoleucine; 40 mg lysine hydrochloride; 30 mg serine; 20 mg each aspartic acid, ...
The least abundant are lysine, methionine, and asparagine. There is less asparagine, isoleucine, and lysine than would be ... Specifically, there is less asparagine, isoleucine, and lysine and more arginine than would be expected for an average protein ...
In N-glycosylation, sugars are attached to nitrogen, typically on the amide side-chain of asparagine. In O-glycosylation, ... For example, inhibition of asparagine-linked, i.e. N-linked, glycosylation can prevent proper glycoprotein folding and full ...
This enzyme participates in alanine and asparagine metabolism. Ibba M, Soll D (2000). "Aminoacyl-tRNA synthesis". Annual Review ... L-asparagine, and tRNAAsx, whereas its 3 products are AMP, diphosphate, and asparaginyl-tRNAAsx. When this enzyme acts on ...
"Glycosidases of the asparagine-linked oligosaccharide processing pathway." Glycobiology 4.2 (1994): 113-125. Herscovics, ...
Asparagine*. N/A. N/A N/A. N/A. N/A. N/A. N/A. N/A. N/A. N/A. N/A. N/A ...
Asparagine Asn N MT-TN 5,657-5,729 H Aspartic acid Asp D MT-TD 7,518-7,585 L ...
Asparagine. Asp. -. NMDA receptors. Small: Amino acids. Glutamate. Glu. Metabotropic glutamate receptors. NMDA receptors, ...
Otherwise histidine, glutamate, asparagine, cysteine are susceptible to methylation. Some of these products include S- ...
... and asparagine". The Biochemistry of Plants. 16: 121-159. Robinson, S. A.; Slade, A. P.; Fox, G. G.; Phillips, R.; Ratcliffe, R ...
"Entrez Gene: asparagine-linked glycosylation 13 homolog (S. cerevisiae)". Gao XD, Tachikawa H, Sato T, Jigami Y, Dean N ( ... It heterodimerizes with asparagine-linked glycosylation 14 (ALG14) homolog to form a functional UDP-GlcNAc glycosyltransferase ... UDP-N-acetylglucosamine transferase subunit ALG13 homolog, also known as asparagine-linked glycosylation 13 homolog, is an ...
Identification of asparagine as the site of ADP-ribosylation". J Biol Chem. 1984;259:749-756. Scovassi, AI; Denegri, M; ... and asparagine have been identified in subsequent works. During DNA damage or cellular stress PARPs are activated, leading to ...
Short day length promotes asparagine formation, whereas glutamine is produced under long day regimes. Darkness favors protein ... Low night temperature conserves glutamine; high night temperature increases accumulation of asparagine because of breakdown. ... breakdown accompanied by high asparagine accumulation. Night temperature modifies the effects due to night length, and soluble ...
The aspartate metabolic pathway is involved in both storage of asparagine and in synthesis of aspartate-family amino acids. ... At night, aspartate is converted to asparagine for storage. Additionally, the aspartate kinase-homoserine dehydrogenase gene is ...
... and asparagine residues. Asparagine, histidine, and arginine residues are involved in catalysis. Human PanK-II isoforms PanK1α ... The middle of the helices is attached by hydrogen bonds between asparagine residues. At the N-terminal end, each helix widens ...
AAA as an asparagine codon in some animal mitochondria. Ohama, T, S. Osawa, K. Watanabe, T.H. Jukes, 1990. J. Molec Evol. 30 ... Asparagine (Asn, N), Aspartic acid (Asp, D), Cysteine (Cys, C), Glutamic acid (Glu, E), Glutamine (Gln, Q), Glycine (Gly, G), ...
"Entrez Gene: asparagine-linked glycosylation 14 homolog (S. cerevisiae)". Chantret I, Dancourt J, Barbat A, Moore SE (March ... Asparagine (N)-glycosylation is an essential modification that regulates protein folding and stability. ALG13 and ALG14 (this ...
... asparagine mutant". Biochemistry. 36 (46): 13979-88. doi:10.1021/bi971004s. PMID 9369469.. ...
2004). "The GTPase-activating protein Rap1GAP uses a catalytic asparagine". Nature. 429 (6988): 197-201. Bibcode:2004Natur.429 ...
... asparagine synthetase (glutamine-hydrolysing), glutamine-dependent asparagine synthetase, asparagine synthetase B, AS, AS-B) is ... AMP + diphosphate + L-asparagine + L-glutamate (overall reaction). (1a) L-glutamine + H2O ⇌. {\displaystyle \rightleftharpoons ... AMP + diphosphate + L-asparagine. The enzyme from Escherichia coli has two active sites6]. ... Asparagine+synthase+(glutamine-hydrolysing) at the US National Library of Medicine Medical Subject Headings (MeSH) ...
Since the asparagine side-chain can form hydrogen bond interactions with the peptide backbone, asparagine residues are often ... The determination of asparagines structure required decades of research. The empirical formula for asparagine was first ... The enzyme asparagine synthetase produces asparagine, AMP, glutamate, and pyrophosphate from aspartate, glutamine, and ATP. In ... Glutamine donates an ammonium group, which reacts with β-aspartyl-AMP to form asparagine and free AMP. Asparagine usually ...
Fructose-asparagine can be prepared by refluxing D-glucose with sodium bisulfite in methanol, and then adding L-asparagine, and ... However, this is not due to fructose-asparagine being an essential nutrient, but rather because fructose-asparagine is toxic to ... contributes to fructose-asparagine but not asparagine utilization". Journal of Bacteriology. 199 (22): e00330-17. doi:10.1128/ ... Fructose-asparagine is a aminodeoxysugar. It takes the form of a pale yellow solid. It decomposes above 120 °C. Fructose- ...
Asparagine synthetase deficiency is a condition that causes neurological problems in affected individuals starting soon after ... aspartic acid to the amino acid asparagine.. In addition to being a component of proteins, asparagine helps to break down toxic ... Asparagine Synthetase Deficiency causes reduced proliferation of cells under conditions of limited asparagine. Mol Genet Metab ... Asparagine synthetase deficiency is caused by mutations in a gene called ASNS. This gene provides instructions for making an ...
First isolated in 1932 from asparagus, from which its name is derived, asparagine is widely distributed in plant proteins. It ... Asparagine, an amino acid closely related to aspartic acid, and an important component of proteins. ... are aspartic acid, asparagine, threonine, and methionine. Aspartic acid and asparagine, which occur in large amounts, can be ... More About Asparagine. 1 reference found in Britannica articles. Assorted References. *proteins* In protein: Structures of ...
Asparagine found in meat, eggs and dairy products is important for normal brain development Asparagine, found in foods such as ...
Other names: L-Asparagine, N,N2-bis(trimethylsilyl)-, trimethylsilyl ester; Asparagine, tris-TMS; Asparagine-3TMS ... Asparagine, 3TMS derivative. *Formula: C13H32N2O3Si3 ...
The asparagine amide group is liberated by the reaction catalyzed by asparaginase (ASPG) and also the amino group of asparagine ... A small multigene family encodes isoenzymes of each step of asparagine metabolism in Arabidopsis, except for asparagine ... Asparagine plays a primary role in nitrogen recycling, storage and transport in developing and germinating seeds, as well as in ... Asparagine Metabolic Pathways in Arabidopsis.. Gaufichon L1, Rothstein SJ2, Suzuki A3. ...
Asparagine, the beta-amido derivative of aspartic acid, is considered a non-essential amino acid. This amino acid plays an ... Asparagine, the beta-amido derivative of aspartic acid, is considered a non-essential amino acid. This amino acid plays an ... On a per-mole basis, asparagine is incorporated into proteins and enzymes at a rate of 4.4 percent with respect to the other ...
Here we demonstrate a role of translational reprogramming in the survival of asparagine-restricted cancer cells. Asparagine ... These studies reveal an axis of adaptation to asparagine deprivation and present a rationale for clinical evaluation of MAPK ... Translational reprogramming during asparagine restriction, via activated MAPK signalling and enhanced translation of activating ... MAPK inhibition attenuates translational induction of ATF4 and the expression of its target asparagine synthetase (ASNS), ...
S)-2-Aminosuccinic acid 4-amide, L-Aspartic acid 4-amide, L-Asparagine ...
This page features an image of asparagine (an amino acid) mixed with and acetaminophen (a common medication). ... Asparagine-Acetaminophen Mixture. Asparagine is one of twenty primary amino acids that occurs naturally in proteins. ... As a crucial building block in major biochemical pathways, asparagine is vital for the metabolism of ammonia in the liver, and ... Interestingly, aspartic acid and asparagine are found in high concentrations in the hippocampus, which is the portion of the ...
L-Asparagine ≥98% (HPLC); CAS Number: 70-47-3; EC Number: 200-735-9; Synonyms: (S)-2-Aminosuccinic acid 4-amide,L-Aspartic acid ... L-asparagine has been used:. *to identify and quantify free amino acids released upon oxidation of proteins and peptides by ... L-asparagine is an uncharged derivative of aspartate. It possesses a polar side chain and is a non-essential amino acid. ...
Asparagine 42 of the conserved endo-inulinase INU2 motif WMNDPN from Aspergillus ficuum plays a role in activity specificity. * ... Vandamme, A. M., Michaux, C., Mayard, A., & Housen, I. (2013). Asparagine 42 of the conserved endo-inulinase INU2 motif WMNDPN ...
Nα-Acetyl-L-asparagine for your research needs. Find product specific information including CAS, MSDS, protocols and references ... Amino Acids & Derivatives, Asparaginase II, Asparagine, Biochemicals and Reagents, Chemical Biology, Chemical Synthesis, Enzyme ...
Rabbit recombinant monoclonal Asparagine synthetase antibody [EP282Y] validated for WB, IHC, ICC/IF and tested in Human, Mouse ... Amino-acid biosynthesis; L-asparagine biosynthesis; L-asparagine from L-aspartate (L-Gln route): step 1/1. ... Anti-Asparagine synthetase antibody [EP282Y] (ab40850) at 1/2000 dilution + K562 cell lysate at 10 µg. Predicted band size : 61 ... Anti-Asparagine synthetase antibody (Alexa Fluor® 647) [EP282Y] (ab207508). Our RabMAb® technology is a patented hybridoma- ...
The amino acid asparagine was until now considered non-essential because it is produced naturally by the body. However, ... For example, asparagine supplement could be given to infants to ensure an adequate level of asparagine in the brain and the ... Asparagine essential for brain development. The amino acid asparagine was until now considered non-essential because it is ... "The cells of the body can do without it because they use asparagine provided through diet. Asparagine, however, is not well ...
Compare Asparagine synthetase ELISA Kits from leading suppliers on Biocompare. View specifications, prices, citations, reviews ... Asparagine synthetase ELISA Kits. The ELISA (enzyme-linked immunosorbent assay) is a well-established antibody-based tool for ... Your search returned 68 Asparagine synthetase ELISA ELISA Kit across 6 suppliers. ...
Properties and functions of asparagine, a non-essential amino acid with a great importance for brain functioning and muscle ... Properties of asparagine. Asparagus is very rich in aspartic acid, a derivative of the amino acid asparagine.. Asparagine has ... Characteristics of asparagine. What is asparagine?. Asparagine is an amino acid from the metabolism of other amino acids, which ... Contraindications of asparagine. Pregnant women or people suffering from liver and kidney diseases should not take asparagine ...
... Mol Microbiol. 1996 Jun;20(5):1001-11. ... aspartate or asparagine; it was resistant to toxic analogues of Glu, Asp, and Asn at concentrations that inhibited growth of ...
Distribution of glutamine and asparagine residues and their near neighbors in peptides and proteins.. A B Robinson and L R ... Distribution of glutamine and asparagine residues and their near neighbors in peptides and proteins. ... Distribution of glutamine and asparagine residues and their near neighbors in peptides and proteins. ... Distribution of glutamine and asparagine residues and their near neighbors in peptides and proteins. ...
In this matter, asparagine attached to anionic linear globular dendrimer G2 (as a biocompatible, biodegradable, and cost- ... Observations revealed that, in addition to successful colon cancer and brain targeting, Gd,sup,3+,/sup,-dendrimer-asparagine, ... Totally, Gd3+-anionic linear globular dendrimer G2-asparagine could be introduced to the cancer imaging/therapy (theranostics) ... for dendrimer, asparagine, and dendrimer-asparagine emphasizes dendrimer-asparagine complexs establishment.. 3.3. Gadolinium ...
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Browse our Asparagine synthetase product catalog backed by our Guarantee+. ... Diseases related to Asparagine synthetase. Discover more about diseases related to Asparagine synthetase.. Leukemia. Malignant ... PTMs for Asparagine synthetase. Learn more about PTMs related to Asparagine synthetase.. Phosphorylation. Acetylation. ... Asparagine synthetase (AS) is a housekeeping enzyme responsible for the production of asparagine from aspartate and glutamine. ...
Belongs to the asparagine synthetase family.ARBA annotation. Automatic assertion according to rulesi ... Amino-acid biosynthesis, Asparagine biosynthesisUniRule annotation. Automatic assertion according to rulesi ... tr,A0A328GGJ6,A0A328GGJ6_MYCTX Asparagine synthetase B OS=Mycobacterium tuberculosis variant pinnipedii OX=194542 GN=asnB PE=3 ...
... to Asparagine synthetase ( P08243,biological,biology supply,biology supplies,biology product ... Rabbit Anti-Asparagine synthetase Monoclonal Antibody, Unconjugated, Clone EP282Y from Abcam,Rabbit monoclonal [EP282Y] ... Antigen: Synthetic peptide corresponding to residues in the C-terminus of Human Asparagine synthetase. Entrez GeneID: 440 SWISS ... Rabbit monoclonal [EP282Y] to Asparagine synthetase (Abpromise for all tested applications). ...
Asparagine Hydroxylation of the HIF Transactivation Domain: A Hypoxic Switch. By David Lando, Daniel J. Peet, Dean A. Whelan, ... Asparagine Hydroxylation of the HIF Transactivation Domain: A Hypoxic Switch. By David Lando, Daniel J. Peet, Dean A. Whelan, ... Asparagine 851 in HIF-2α is highly conserved across species, as is the equivalent Asn803 in HIF-1α (Fig. 3A), suggesting that ... Asparagine Hydroxylation of the HIF Transactivation Domain: A Hypoxic Switch Message Subject. (Your Name) has forwarded a page ...
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1A85: Structure of malonic acid-based inhibitors bound to human neutrophil collagenase. A new binding mode explains apparently anomalous data.
Asparagine is not an essential amino acid. Asparagine is produced when sugars react to heat, for example: baked goods, potato ... Asparagus contains the highest amount of asparagine, where the name comes from. Other foods that contain asparagine include: ... Amino Acid Asparagine, Asparaginy aminokwasów, Asparagine एमिनो एसिड, Aminoácido asparagina, Аспарагин Аминокислоты, Ασπαραγίνη ... Other names: Aspartic Acid, Asparagine. Translations: Asparagīna Amino Acid, Asparaginas aminorūgšties, Asparagina aminoacizi, ...
  • In return, bacteroids act like plant organelles to cycle amino acids back to the plant for asparagine synthesis. (ox.ac.uk)
  • 0.790g asparagine and 0.294g hydroxyproline (both free form amino acids) were found. (priceplow.com)
  • It is also a source of essential amino acids such as leucine, aspartic acid and asparagine. (antakiayoresel.com)
  • The asparagine residue is highly conserved and there is a small physicochemical difference between asparagine and threonine. (utah.edu)
  • This mutation replaces the amino acid asparagine with the amino acid aspartic acid at protein position 314 (written as Asn314Asp or N314D). (medlineplus.gov)
  • Its use in anti-cancer therapy is based on its ability to cleave L-asparagine, an amino acid essential for the growth of lymphoblasts, to ammonia and L-aspartic acid in serum and cerebrospinal fluid. (pjmonline.org)
  • L-asparaginase, produced mainly by microrganisms, cleaves L-asparagine to aspartic acid and ammonia as products. (sci-rep.com)
  • The filtrate was used to determine the L-asparaginase activity through the hydroximate aspartic methodology using L-asparagine as substrate. (sci-rep.com)
  • This sequence change replaces aspartic acid with asparagine at codon 181 of the SDHB protein (p.Asp181Asn). (utah.edu)
  • The present structures in a lipid bilayer revealed the detailed mechanism for the tetrameric assembly of PepT So2 , in which a characteristic extracellular loop (ECL) interacts with two asparagine residues on H12 which were reported to be important for tetramerization and plays an essential role in oligomeric assembly. (rcsb.org)
  • The Protein Deglycosylation Mix II includes the enzymes necessary to remove carbohydrates attached to Asparagine residues, simple core 1 and core 3 O-linked carbohydrates attached to Ser/Thr, and decorated core 1 and 3 O-glycans (with lactosamine extensions). (neb.com)
  • Residues with low binding energy to asparagine (Asn) and high binding energy to glutamine (Gln) were chosen for mutagenesis. (waocp.org)
  • The Company's lead product candidate, eryaspase, which consists of L-asparaginase encapsulated inside donor-derived red blood cells, targets the cancer cell's altered asparagine and glutamine metabolism. (yahoo.com)
  • Ryder, now 4.5 years old, had a condition called Asparagine Synthetase Deficiency Disorder. (cincinnatichildrens.org)
  • Asparagine synthetase (ASNS) catalyses the ATP-dependent conversion of aspartate to asparagine. (biocytogen.com)
  • The asparagine at codon 194 is replaced by threonine, an amino acid with similar properties. (utah.edu)
  • This sequence change replaces asparagine with threonine at codon 194 of the TNNI3 protein (p.Asn194Thr). (utah.edu)
  • Thus, we found that p53 regulates asparagine metabolism and dictates cell survival by generating an auto-amplification loop via asparagine-aspartate-mediated LKB1-AMPK signalling. (biocytogen.com)
  • Our findings highlight a role for LKB1 in sensing asparagine and aspartate and connect asparagine metabolism to the cellular signalling transduction network that modulates cell survival. (biocytogen.com)
  • This sequence change replaces asparagine with lysine at codon 436 of the DSG2 protein (p.Asn436Lys). (utah.edu)
  • The syntheses and crystal structures of six substituted benzenesulfonyl-asparagine derivatives are reported. (elsevier.com)
  • This sequence change replaces asparagine with serine at codon 162 of the BBS2 protein (p.Asn162Ser). (utah.edu)
  • Here, we report that p53 suppresses asparagine synthesis through the transcriptional downregulation of ASNS expression and disrupts asparagine-aspartate homeostasis, leading to lymphoma and colon tumour growth inhibition in vivo and in vitro. (biocytogen.com)
  • Acrylamide forms when the amino acid asparagine reacts with sugar in foods. (vitacost.com)
  • The application protects the company's work over the last two years in developing baker's yeast strains (Saccharomyces cerevisiae) that reduces acrylamide by up to 95 per cent in a variety of food products by degrading the precursor compound asparagine. (foodmag.com.au)
  • Acrylamide is not added to foods, but forms naturally from the amino acid asparagine when foods are heated above 120 °C (e.g. baking, roasting, or frying). (foodmag.com.au)
  • Renaissance Ingredients' AR yeast strains are traditional baker's yeast with an accelerated natural ability to consume asparagine, thereby reducing acrylamide. (foodmag.com.au)
  • L-asparagine aminohydrolase) catalyzes the deamination of L-asparagine (Asn) to L-aspartate and ammonia. (pjmonline.org)
  • At the time the patent was filed, it was universally believed that the daptomycin compound included the L-isomer of asparagine. (jdsupra.com)
  • In particular, because the "specification as a whole" made clear that the compound being claimed as "Formula 3" was always intended to be the prior art compound daptomycin, "D-asparagine was covered both before and after correction. (jdsupra.com)
  • eIF4B enhances ATF4 expression and contributes to cellular adaptation to asparagine limitation in BRAF-mutated A375 melanoma. (or.jp)
  • Since lymphoblasts are unable to produce endogenous L-asparagine, starvation for this amino acid leads to the death of these cells (Kotzia and Labrou, 2007). (pjmonline.org)
  • Mechanistically, asparagine and aspartate regulate AMPK-mediated p53 activation by physically binding to LKB1 and oppositely modulating LKB1 activity. (biocytogen.com)