Mouse polyclonal antibody raised against a full-length human ZCCHC12 protein. ZCCHC12 (NP_776159.1, 1 a.a. ~ 402 a.a) full-length human protein. (H00170261-B01P) - Products - Abnova

Galactose-1-phosphate uridylyltransferase (or GALT) is an enzyme (EC 2.7.7.12) responsible for converting ingested galactose to glucose. Galactose-1-phosphate uridylyltransferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely: UDP-glucose + galactose 1-phosphate ⇌ {\displaystyle \rightleftharpoons } glucose 1-phosphate + UDP-galactose The expression of GALT is controlled by the actions of the FOXO3 gene. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. galactose glucose GALT catalyzes the second reaction of the Leloir pathway of galactose metabolism through ping pong bi-bi kinetics with a double displacement mechanism. This means that the net reaction consists of two reactants and two products (see the reaction above) and it proceeds by the following mechanism: the enzyme reacts with one ...

Because galactose-1-phosphate uridyl transferase has been reported to be elevated in the blood of patients with mongolism (21 trisomy), assay of this enzyme in the erythrocytes and leukocytes was performed in patients with the Philadelphia chromosome. Twenty normal individuals and 16 patients with the Ph1 chromosome were studied; 15 of the latter had chronic myelogenous leukemia and 1 had an unusual myeloproliferative disorder. The mean leukocyte enzyme level in the Ph1 group was not different from that in the normal group. The mean erythrocyte enzyme level in the Ph1 group was higher than that in the normal group; this difference might have been due to a younger population of red cells in the Ph1 patients.. To interpret the results, three postulates are presented. First, the relationship between chromosome 21 and this enzyme activity may be obscured by other controlling factors. Second, the long arm of this chromosome may play no role in transferase activity. Third, there may be no reduction of ...

A gene encoding glucose-1-phosphate uridylyltransferase (EC 2.7.7.9) was isolated from Streptococcus mutans. A cell extract of Escherichia coli expressing the cloned gene exhibited glucose-1-phosphate uridylyltransferase activity. The enzyme catalyses the conversion of D-glucose 1-phosphate and UTP into UDP-D-glucose. Rabbit antiserum against the serotype-c-specific antigen did not react with autoclaved extracts from mutant cells in which the cloned gene was insertionally inactivated. The glucose content of the cell-wall preparation purified from the mutant was very much lowered, whereas there was no observable decrease in the content of rhamnose. When the mutant strain was grown in an acidic environment, its cell viability was much lower than that of the wild-type. These results suggest that UDP-D-glucose functions not only as an immediate precursor of the serotype-c-specific antigen of S. mutans (as a glucose donor for side-chain formation), but is also important for the organism's viability in

Modifies, by uridylylation and deuridylylation, the PII regulatory proteins (GlnB and homologs), in response to the nitrogen status of the cell that GlnD senses through the glutamine level. Under low glutamine levels, catalyzes the conversion of the PII proteins and UTP to PII-UMP and PPi, while under higher glutamine levels, GlnD hydrolyzes PII-UMP to PII and UMP (deuridylylation). Thus, controls uridylylation state and activity of the PII proteins, and plays an important role in the regulation of nitrogen fixation and metabolism.

Modifies, by uridylylation and deuridylylation, the PII regulatory proteins (GlnB and homologs), in response to the nitrogen status of the cell that GlnD senses through the glutamine level. Under low glutamine levels, catalyzes the conversion of the PII proteins and UTP to PII-UMP and PPi, while under higher glutamine levels, GlnD hydrolyzes PII-UMP to PII and UMP (deuridylylation). Thus, controls uridylylation state and activity of the PII proteins, and plays an important role in the regulation of nitrogen assimilation and metabolism.

d). This pattern is strongly conserved, implying that there is a functional significance to the arrangement. It is possible that the conserved residues define a binding site for an unknown ligand. Since the potential pocket is on the opposite side of the β-sheet to the ATP site, such a ligand might function as an allosteric effector regulating PII function by modulating access to the ATP-binding site. An alternative and more speculative interpretation is that the conserved residues are important in stabilizing a conformational change in the molecule. Such a change might occur during interaction with partner proteins. In this case, the hydrophobic side chains currently separated from one another and forming an open pocket might be brought into contact, forming an interdentate cross-link and making the PII protein significantly more rigid.. The interacting partners of the PII in Neisseria are currently unknown. However, given the structural conservation of the protein, some candidates can be ...

Magrangeas F et al. (1998) Cotranscription and intergenic splicing of human galactose-1-phosphate uridylyltransferase and interleukin-11 receptor alpha-chain genes generate a fusion mRNA in normal cells. Implication for the production of multidomain proteins during evolution.. [^] ...

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UTP-glucose-1-phosphate uridylyltransferase also known as glucose-1-phosphate uridylyltransferase (or UDP-glucose pyrophosphorylase) is an enzyme involved in carbohydrate metabolism. It synthesizes UDP-glucose from glucose-1-phosphate and UTP; i.e., glucose-1-phosphate + UTP ⇌ {\displaystyle \rightleftharpoons } UDP-glucose + pyrophosphate UTP-glucose-1-phosphate uridylyltransferase is an enzyme found in all three domains (bacteria, eukarya, and archaea) as it is a key player in glycogenesis and cell wall synthesis. Its role in sugar metabolism has been studied extensively in plants in order to understand plant growth and increase agricultural production. Recently, human UTP-glucose-1-phosphate uridylyltransferase has been studied and crystallized, revealing a different type of regulation than other organisms previously studied. Its significance is derived from the many uses of UDP-glucose including galactose metabolism, glycogen synthesis, glycoprotein synthesis, and glycolipid synthesis. The ...

contains similarity to Pfam domain PF01704 (UTP--glucose-1-phosphate uridylyltransferase)contains similarity to Interpro domain IPR002618 (UTP--glucose-1-phosphate uridylyltransferase ...

contains similarity to Pfam domain PF01704 (UTP--glucose-1-phosphate uridylyltransferase)contains similarity to Interpro domain IPR002618 (UTP--glucose-1-phosphate uridylyltransferase ...

This fibroblast cell line was established by W.J. Mellman from a skin biopsy of a 6-year-old Black male with galactosemia. This child demonstrated a classic galactosemia picture in infancy and lacks galactose-1-phosphate uridyl transferase activity in his circulating red cells. His older sibling (W.W.) lacks the same enzyme but exhibited no clinical symptoms of galactosemia. [Cell line CHP4, ATCC CCL-133]

A quantitative galactose-1-phosphate uridyltransferase GALT) level is used in addition to the isoelectric focusing for accurate interpretation. If recent GALT test results are not provided, GALT will be automatically performed at an additional charge. However, if previous GALT results are provided, GALT testing will be cancelled and not charged.. See Galactosemia Testing Algorithm in Special Instructions.. ...

Galactose-1-phosphate uridyltransferase is a blood test that measures the level of a substance called GALT, which helps break down milk sugars in your body. A low level of this substance causes a condition called galactosemia.

Staphylococcus aureus; strain: Newman; locus tag: NWMN_RS13790 (NWMN_2395); symbol: gtaB; product: UTP--glucose-1-phosphate uridylyltransferase

Updated: 2019/03/07 14:07:41. Note: The information contained in this handbook is for use by personnel of University of Iowa Health Care. No other use is implied or intended.. Vacutainer® and/or Microtainer® are registered trademarks of Becton, Dickinson & Company.. ...

Cellular adaptability to environmental changes depends on the collective actions of genes, mRNA, proteins and ligands, all of which are components of a genetic network. To understand the dynamics of a gene network in response to temporally and spatially environmental changes, we focus on the galactose utilization network in the yeast Saccharomyces cerevisiae. This network allows yeast cells to metabolize galactose in the absence of glucose and is tightly repressed when glucose is available in the environment. The main question is how the Gal network is activated when glucose is depleted since both sugars cannot be metabolized simultaneously. Using a microfluidic device, we supplied yeast cells with both glucose and galactose before linearly depleting glucose at different rates. We tracked the onset and accumulation of a yellow fluorescent reporter-tagged Gal1p, the first enzyme of the Gal network. Our data shows that the glucose-depletion rate plays an important role in the activation of the ...

1HM8: Crystal structure of Streptococcus pneumoniae N-acetylglucosamine-1-phosphate uridyltransferase bound to acetyl-coenzyme A reveals a novel active site architecture.

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SWISS-MODEL Template Library (SMTL) entry for 4ud4.1. Structural Plasticity of Cid1 Provides a Basis for its RNA Terminal Uridylyl Transferase Activity

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Fortunato, E., Gaspar, D., Duarte, P., Pereira, L., Águas, H., Vicente, A., Dourado, F., Gama, M. & Martins, R., 11 Jul 2016, Bacterial Nanocellulose: From Biotechnology to Bio-Economy. Elsevier Inc., 19 p.. Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review ...

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Fast delivery of ZCCHC5 knockout Human Cell Lines for the study of gene function. Created by CRISPR/Cas9 genome editing. Includes matched wildtype control.

Human ZCCHC6 full-length ORF ( AAH32456.1, 1 a.a. - 412 a.a.) recombinant protein with GST-tag at N-terminal. (H00079670-P01) - Products - Abnova

Complete information for ZCCHC12 gene (Protein Coding), Zinc Finger CCHC-Type Containing 12, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Looking for online definition of galactose 1-phosphate uridylyltransferase in the Medical Dictionary? galactose 1-phosphate uridylyltransferase explanation free. What is galactose 1-phosphate uridylyltransferase? Meaning of galactose 1-phosphate uridylyltransferase medical term. What does galactose 1-phosphate uridylyltransferase mean?

Classic galactosemia (OMIM 230400) is an autosomal recessive disorder that results from profound impairment of galactose-1-phosphate uridylyltransferase (GALT, EC 2.7.7.12), the middle enzyme in the Leloir pathway of galactose metabolism (see review by Fridovich-Keil and Walter, 2008). In most western populations, classic galactosemia occurs with a frequency of at least 1/60,000 live births; the rate is substantially higher in some groups. Infants with classic galactosemia generally appear normal at birth but present with escalating symptoms within days of exposure to dietary galactose, which, as a constituent monosaccharide of lactose, is abundant in breast milk and milk-based formulae. Acute symptoms range from cataracts, failure to thrive, vomiting and diarrhea to hepatomegaly, bleeding abnormalities and Escherichia coli sepsis, which can be lethal. Absent intervention, infants with classic galactosemia often succumb in the neonatal period (see review by Fridovich-Keil and Walter, ...

K01187 malZ; alpha-glucosidase [EC:3.2.1.20] K01187 malZ; alpha-glucosidase [EC:3.2.1.20] K01187 malZ; alpha-glucosidase [EC:3.2.1.20] K01187 malZ; alpha-glucosidase [EC:3.2.1.20] K00963 UGP2; UTP--glucose-1-phosphate uridylyltransferase [EC:2.7.7.9] K00963 UGP2; UTP--glucose-1-phosphate uridylyltransferase [EC:2.7.7.9] K05349 bglX; beta-glucosidase [EC:3.2.1.21] K05350 bglB; beta-glucosidase [EC:3.2.1.21] K05350 bglB; beta-glucosidase [EC:3.2.1.21] K01179 E3.2.1.4; endoglucanase [EC:3.2.1.4] K19668 CBH2; cellulose 1,4-beta-cellobiosidase [EC:3.2.1.91] K01222 E3.2.1.86A; 6-phospho-beta-glucosidase [EC:3.2.1.86] K01222 E3.2.1.86A; 6-phospho-beta-glucosidase [EC:3.2.1.86] K00700 GBE1; 1,4-alpha-glucan branching enzyme [EC:2.4.1.18] K00700 GBE1; 1,4-alpha-glucan branching enzyme [EC:2.4.1.18] K00688 PYG; glycogen phosphorylase [EC:2.4.1.1] K01176 AMY; alpha-amylase [EC:3.2.1.1] K05343 treS; maltose alpha-D-glucosyltransferase / alpha-amylase [EC:5.4.99.16 3.2.1.1] K05343 treS; maltose ...

K01187 malZ; alpha-glucosidase [EC:3.2.1.20] K00963 UGP2; UTP--glucose-1-phosphate uridylyltransferase [EC:2.7.7.9] K00963 UGP2; UTP--glucose-1-phosphate uridylyltransferase [EC:2.7.7.9] K05349 bglX; beta-glucosidase [EC:3.2.1.21] K05349 bglX; beta-glucosidase [EC:3.2.1.21] K05350 bglB; beta-glucosidase [EC:3.2.1.21] K01179 E3.2.1.4; endoglucanase [EC:3.2.1.4] K00703 glgA; starch synthase [EC:2.4.1.21] K00693 GYS; glycogen synthase [EC:2.4.1.11] K00700 GBE1; 1,4-alpha-glucan branching enzyme [EC:2.4.1.18] K00688 PYG; glycogen phosphorylase [EC:2.4.1.1] K01176 AMY; alpha-amylase [EC:3.2.1.1] K05343 treS; maltose alpha-D-glucosyltransferase / alpha-amylase [EC:5.4.99.16 3.2.1.1] K05343 treS; maltose alpha-D-glucosyltransferase / alpha-amylase [EC:5.4.99.16 3.2.1.1] K21574 susB; glucan 1,4-alpha-glucosidase [EC:3.2.1.3] K01182 IMA; oligo-1,6-glucosidase [EC:3.2.1.10] K00705 malQ; 4-alpha-glucanotransferase [EC:2.4.1.25] K16147 glgE; starch synthase (maltosyl-transferring) [EC:2.4.99.16] K00691 ...

Classic galactosemia type I is a metabolic disorder. It causes a low level or lack of an enzyme called galactose-1-phosphate uridyltransferase. This enzyme changes galactose to glucose. Galactose is a simple sugar found in milk products. Glucose is the usable form of sugar in the human body. Since there is not enough of the enzyme, galactose builds up in the blood. This build up can cause severe damage to the liver, kidneys, central nervous system, and other body systems. If undetected, galactosemia is fatal. Type II is a less severe form of this disease due to low levels of galactose kinase. This type may be managed with a few dietary restrictions. It does not carry the risk of neurologic or liver damage. Type III is a form with variable severity due to low levels of galactose epimerase. This type can cause cataracts, delayed growth and development, intellectual disability, liver disease, and kidney problems. This sheet will focus on classic galactosemia.

Dr Lal PathLabs GALACTOSEMIA PANEL 1 in Bangalore is health checkup package includes 4 Tests. ₹100 Cashback and Free Doctor Consultation, Home sample collection and Online reports available. GALACTOSEMIA PANEL 1 in Bangalore covers 4 parameters- GALACTOSEMIA SCREENING, METHOD GALACTOSEMIA PANEL 1 in Bangalore, Patient Value, CONTROL VALUE

Dr Lal PathLabs GALACTOSEMIA PANEL 1 is health checkup package includes 4 Tests. Rs.100 Cashback and Free Doctor Consultation, Free Home sample collection and Online reports available. GALACTOSEMIA PANEL 1 covers 4 parameters- GALACTOSEMIA SCREENING, METHOD GALACTOSEMIA PANEL 1, Patient Value, CONTROL VALUE

In 1931, in a paper on the study of the metabolism of galactose in the human subject, Shay, Schloss and Bell1 concluded that this hexose was best suited for testing the carbohydrate function of the liver. In order for the urinary excretion of this sugar, orally administered, to act as a measure of hepatic carbohydrate function, they considered the following among the necessary conditions: (1) that there be no renal threshold for the excretion of galactose; (2) that galactose utilization remain unmodified by the activity of those endocrine glands known to affect glucose metabolism; (3) that galactose be practically unutilizable ...

Galctose-1-phosphate uridyltransferase (GALT) is an enzyme responsible for one step in this process. When this is absent/deficient galactose cannot be changed to glucose and results in a number of clinical abnormalities. Galactosemia quantitation is a blood test that checks the levels of the enzyme known as GALT.

TY - JOUR. T1 - Ultrasensitive capillary electrophoretic analysis of potentially immunogenic carbohydrate residues in biologics. T2 - Galactose-α-1,3-galactose containing oligosaccharides. AU - Szabo, Zoltan. AU - Guttman, Andras. AU - Bones, Jonathan. AU - Shand, Randi L.. AU - Meh, David. AU - Karger, Barry L.. PY - 2012/6/4. Y1 - 2012/6/4. N2 - With the recent growth of the global monoclonal antibody market, ultrasensitive techniques are required for rapid analysis of possible immunogenic residues, such as galactose-α-1,3-galactose (α-1,3-Gal) on therapeutic proteins expressed in murine or CHO cell lines. We report a capillary electrophoretic approach in conjunction with exoglycosidase digestion for structural elucidation of IgG N-glycans containing the above immunogenic epitope. The method uses commercially available reagents and instrumentation, thus making it readily available for implementation and validation within the biotechnology industry. The method was first evaluated using ...

This gene encodes a member of the galactose-3-O-sulfotransferase protein family. The product of this gene catalyzes sulfonation by transferring a sulfate group to the 3 position of galactose in N-acetyllactosamine in both type 2 (Gal-beta-1-4GlcNAc-R) oligosaccharides and core-2-branched O-glycans, but not on type 1 or core-1-branched structures. This gene, which has also been referred to as GAL3ST2, is different from the GAL3ST2 gene located on chromosome 2 that encodes a related enzyme with distinct tissue distribution and substrate specificities, compared to galactose-3-O-sulfotransferase 3. [provided by RefSeq, Jul 2008 ...

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Explains test for galactosemia, a rare disease passed from parents to children. Covers blood or urine test that checks a newborn for enzymes needed to change galactose from milk into glucose, a sugar used for energy. Explains why and how the test is done.

Dr. Lester Thompson answered: Inherited: Galactosemia is a autosomal recessive inherited condition which causes you to metabolise ...

Learn more about Galactosemia at Doctors Hospital of Augusta DefiniciónCausasFactores de riesgoSíntomasDiagnósticoTratamientoPrevenció...

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We examine the application of statistical model selection methods to reverse-engineering the control of galactose utilization in yeast from DNA microarray experiment data. In these experiments, relationships among gene ...

Arginine Alpha Ketoglutarate joaca un rol important in volumizarea celulelor, astfel incat nutrientii sunt transportati mai bine in muschi. Din acest motiv, Arginine Alpha Ketoglutarate de la MyProtein este un supliment care ajuta la imbunatatirea performantelor fizice si sprijina refacerea musculara dupa antrenament ...

Learn about the causes, symptoms, diagnosis & treatment of Inherited Disorders of Metabolism from the Professional Version of the Merck Manuals.

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Styles tend to not only separate men - because they have their own doctrines and then the doctrine became the gospel truth that you cannot change. But if you do not have a style, if you just say: Well, here I am as a human being, how can I express myself totally and completely? Now, that way you wont create a style, because style is a crystallization. That way, its a process of continuing growth ...

Complete information for ZCCHC18 gene (Protein Coding), Zinc Finger CCHC-Type Containing 18, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Recombinant alpha Ketoglutarate Dehydrogenase (alphaKGDHC) Protein (His tag). Species: Mouse (Murine). Source: Insect Cells. Order product ABIN3135266.

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517 (12 years ago) by duarte: Changed Alignment class so that both alignment and sequence indexing are starting at 1 (before alignment indices were starting at 0). Also mapping is now done through arrays not maps. Changed all other classes using Alignment to accommodate this. NOTE: graph averaging hasnt been tested after the change ...

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DB-ID: Database ID of variant, grouping multiple observations of the same variant together, starting with the HGNC gene symbol, followed by an underscore (_) and a six digit number (e.g. DMD_012345). _000000 is used for variants where DNA was not analysed (change predicted from RNA analysis), variants seen in animal models or variants not seen in humans but functionally tested in vitro ...

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Selecting of format.. Clicking one of the Downlod boxes will download a file in the corresponding format with the selected data columns for the genes shown in the search result.. The copy boxes will give you a link to the file if you want to share it or save for later as a reference. ...

Use Bio-Rads PrimePCR assays, controls, templates for your target gene. Every primer pair is optimized, experimentally validated, and performance guaranteed.