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34 Possible Causes for activity, glycolipid, sulfotransferase

  • Alpha-Galactosidase

    Background: GCase activity measured in dried blood spots of PD cases is reduced compared to controls.[n.neurology.org] There is no urinary excretion of glycolipids or mucopolysaccharides. Yet this patient has an accumulation of material in his fibroblasts and renal cells.[ncbi.nlm.nih.gov] […] was sulfated and the percent of enzyme sulfation decreased with increasing amplification, presumably due to the inaccessibility of the enzyme's tyrosine residues for the sulfotransferase[jcb.rupress.org]

  • Metachromatic Leukodystrophy

    SapB-d) are both lipid storage disorders caused by mutations in the PSAP gene that codes for the 65-70 kDa prosaposin protein, which is the precursor for four sphingolipid activator[ncbi.nlm.nih.gov] This disorder is characterized by the lysosomal accumulation of sulfated glycolipids, specifically 3- O -sulfogalactosyl-containing glycolipids (galactocerebroside sulfate[themedicalbiochemistrypage.org] Leyh, Ian Cook and Ting Wang , Structure, dynamics and selectivity in the sulfotransferase family , Drug Metabolism Reviews , 45 , 4 , (423) , (2013) .[doi.org]

  • Bacillus Subtilis

    Membrane lipids, phospholipids, and glycolipids are synthesized from fatty acids.[doi.org] In addition, the cultures showed cellulase activity in carboxy methyl cellulose medium (1.5-1.8mg of reducing sugar24h(-1)ml(-1)) and amylase activity in vitro.[ncbi.nlm.nih.gov] […] peptide binding to S. aureus adhesin SdrC 33 In stock BBa_K1351001 Contactin-4-derived peptide binding to NADH Oxidase of S. pneumoniae 42 In stock BBa_K1351002 Chondroitin 4 sulfotransferase-derived[parts.igem.org]

  • Adenosine

    KEY FINDINGS: Results show that the anticancer effect is not due to A 3 AR activation alone.[ncbi.nlm.nih.gov] Invariant NKT (iNKT) cells A rare subset of lymphocytes that expresses an invariant T-cell receptor that recognizes certain glycolipids when bound to the major histocompatibility[doi.org] By coupling IMPAD1 to the AMP-Glo system, we can measure the activities of sulfotransferases.[ncbi.nlm.nih.gov]

  • Mevalonate Kinase Deficiency

    Finally, we show that pharmacological inactivation of RhoA boosts Rac1 activity, a small GTPase whose activity was earlier implied in MKD pathogenesis.[ncbi.nlm.nih.gov] […] diseases [BR: br08402 ] Immune system diseases Other immune system diseases H00206 Mevalonate kinase deficiency Congenital disorders of metabolism Congenital disorders of lipid/glycolipid[genome.jp] […] nucleosidase Deficiency of amylase Deficiency of amylo-1,6-glucosidase Deficiency of arginine deiminase Deficiency of aromatic-L-amino-acid decarboxylase Deficiency of aryl sulfotransferase[icd9data.com]

  • Eubacterium

    Strain BBSH 797 to the list of active constituents not requiring evaluation.[apvma.gov.au] L-fucose is a desoxyhexose that is a common component of many N- and O-linked glycans and of glycolipids produced by mammalian cells ( Becker and Lowe, 2003 ).[frontiersin.org] Sulfotransferase production was strongly inhibited by phenylphosphate esters.[ncbi.nlm.nih.gov]

  • Farber Disease

    These cells accumulate ceramide as the result of genetic deficiency of acid ceramidase and the ceramidase activator (sap-D), respectively.[ncbi.nlm.nih.gov] One is that the accumulation of glycolipids such as sulfatide and GM3 ganglioside is a secondary event produced by the accumulation of ceramide due to ceramidase deficiency[ncbi.nlm.nih.gov] ., progeroide Form Galactosyltransferase I B4GALT7 5q35.2-q35.3 Spondyloepiphyseale Dysplasie, Typ Omani Chondroitin-6-Sulfotransferase CHST3, C6ST, C6ST1, HSD 10q22.1 Mucopolysaccharidose[de.wikibooks.org]

  • Myoadenylate Deaminase Deficiency

    Adenylate deaminase activity was much lower in cultured human muscle cells than in normal muscle. The activity increased with maturation.[ncbi.nlm.nih.gov] It is worth bearing in mind, however, that not only glycogen but other polysaccharides, as well as neutral mucopolysaccharides, muco- and glycoproteins, glycolipids and some[sites.google.com] […] nucleosidase Deficiency of amylase Deficiency of amylo-1,6-glucosidase Deficiency of arginine deiminase Deficiency of aromatic-L-amino-acid decarboxylase Deficiency of aryl sulfotransferase[icd9data.com]

  • Leishmania

    Terminal, non-reducing, and linear α-galactopyranosyl (α-Gal) epitopes are abundantly found on the plasma membrane glycolipids of L. major known as glycoinositolphospholipids[ncbi.nlm.nih.gov] Moreover, a recombinant gp63 protein was produced and its COX activity tested, confirming that gp63 is the molecule responsible for COX activity.[ncbi.nlm.nih.gov] METHODS: Chemical libraries have been screened against the anti-targets pregnane-X-receptor, sulfotransferase, cytochrome P450 2a6, 2c9, and 3a4 with three different docking[ncbi.nlm.nih.gov]

  • Mannose-Binding Lectin Deficiency

    To examine this hypothesis, complement activation by MBL-binding ligands was studied.[ncbi.nlm.nih.gov] W, D 1 Kruckenberger impact P., Different sialyltransferase activities in human colorectal carcinoma cells from surgical specimens detected by specific glycoprotein and glycolipid[google.dk] It is capable of binding to other repeated structures of sugars present in a wide variety of bacteria and other microorganisms, promoting their elimination by the activation[oalib.com]