Uridine diphosphate galactoseGlcA-beta-(1-2)-D-Man-alpha-(1-3)-D-Glc-beta-(1-4)-D-Glc-alpha-1-diphospho-ditrans,octacis-undecaprenol 4-beta-mannosyltransferase: GlcA-beta-(1->2)-D-Man-alpha-(1->3)-D-Glc-beta-(1->4)-D-Glc-alpha-1-diphospho-ditrans,octacis-undecaprenol 4-beta-mannosyltransferase (, GumI) is an enzyme with system name GDP-mannose:GlcA-beta-(1->2)-D-Man-alpha-(1->3)-D-Glc-beta-(1->4)-D-Glc-alpha-1-diphospho-ditrans,octacis-undecaprenol 4-beta-mannosyltransferase. This enzyme catalyses the following chemical reactionGalactose epimerase deficiencyGlycoside hydrolase family 22: In molecular biology, glycoside hydrolase family 22 is a family of glycoside hydrolases.GalactosemiaGalactoseSoyasapogenol glucuronosyltransferase: Soyasapogenol glucuronosyltransferase (, UGASGT) is an enzyme with system name UDP-D-glucuronate:soyasapogenol 3-O-D-glucuronosyltransferase. This enzyme catalyses the following chemical reactionUDP-D-xylose:beta-D-glucoside alpha-1,3-D-xylosyltransferase: UDP-D-xylose:beta-D-glucoside alpha-1,3-D-xylosyltransferase (, beta-glucoside alpha-1,3-xylosyltransferase) is an enzyme with system name UDP-alpha-D-xylose:beta-D-glucoside 3-alpha-D-xylosyltransferase. This enzyme catalyses the following chemical reactionUridine diphosphate glucuronic acidA-1,4-glucan-protein synthase (UDP-forming): Alpha-1,4-glucan-protein synthase (UDP-forming) (, UDP-glucose:protein glucosyltransferase, glycogen initiator synthase, UDPGlc:protein transglucosylase, UPTG, uridine diphosphoglucose protein transglucosylase I, proglycogen synthase, uridine diphosphoglucose-protein 4-alpha-glucosyltransferase, uridine diphosphoglucose-protein glucosyltransferase, UDP-glucose protein transglucosylase, UDP-glucose-protein glucosyltransferase, uridine diphosphate glucose-protein transglucosylase I) is an enzyme with system name UDP-glucose:protein 4-alpha-glucosyltransferase. This enzyme catalyses the following chemical reactionGalactose oxidase: Galactose oxidase (D-galactose:oxygen 6-oxidoreductase, D-galactose oxidase, beta-galactose oxidase; abbreviated GAO, GAOX, GOase; ) is an enzyme that catalyzes the oxidation of D-galactose in some species of fungi.Pyrimidine metabolism: Pyrimidine biosynthesis occurs both in the body and through organic synthesis.D-xylose reductase: D-xylose reductase (, XylR, XyrA, msXR, dsXR, monospecific xylose reductase, dual specific xylose reductase, NAD(P)H-dependent xylose reductase, xylose reductase) is an enzyme with system name xylitol:NAD(P)+ oxidoreductase. This enzyme catalyses the following chemical reactionUridine triphosphateAbscisate beta-glucosyltransferase: Abscisate beta-glucosyltransferase (, ABA-glucosyltransferase, ABA-GTase, AOG) is an enzyme with system name UDP-D-glucose:abscisate beta-D-glucosyltransferase. This enzyme catalyses the following chemical reactionOST4: In molecular biology, OST4 (Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 4) is a subunit of the oligosaccharyltransferase complex.Microsome: In cell biology, microsomes are vesicle-like artifacts re-formed from pieces of the endoplasmic reticulum (ER) when eukaryotic cells are broken-up in the laboratory; microsomes are not present in healthy, living cells.Burst kinetics: Burst kinetics is a form of enzyme kinetics that refers to an initial high velocity of enzymatic turnover when adding enzyme to substrate. This initial period of high velocity product formation is referred to as the "Burst Phase".Ditrans,polycis-polyprenyl diphosphate synthase ((2E,6E)-farnesyl diphosphate specific): Ditrans,polycis-polyprenyl diphosphate synthase ((2E,6E)-farnesyl diphosphate specific) (, RER2, Rer2p, Rer2p Z-prenyltransferase, Srt1p, Srt2p Z-prenyltransferase, ACPT, dehydrodolichyl diphosphate synthase 1) is an enzyme with system name (2E,6E)-farnesyl-diphosphate:isopentenyl-diphosphate cistransferase (adding 10--55 isopentenyl units). This enzyme catalyses the following chemical reactionUndecaprenyl phosphate N,N'-diacetylbacillosamine 1-phosphate transferase: Undecaprenyl phosphate N,N'-diacetylbacillosamine 1-phosphate transferase (, PglC) is an enzyme with system name UDP-N,N'-diacetylbacillosamine:tritrans,heptacis-undecaprenyl-phosphate N,N'-diacetylbacillosamine transferase. This enzyme catalyses the following chemical reactionL-galactose 1-dehydrogenase: L-galactose 1-dehydrogenase (, L-GalDH, L-galactose dehydrogenase) is an enzyme with system name L-galactose:NAD+ 1-oxidoreductase. This enzyme catalyses the following chemical reactionSteptoean positive carbon isotope excursion: The Steptoean Positive Carbon Isotope Excursion (SPICE) was a geological event which occurred about 500 million years ago at the end of the Cambrian Period. The SPICE event was a sudden reversal of the anoxia (lack of oxygen) that had steadily spread throughout the oceans during the Cambrian which also affected the atmosphere.BilirubinNucleoside-diphosphate kinase: Nucleoside-diphosphate kinases (NDPKs, also NDP Kinase, (poly)nucleotide kinases and nucleoside diphosphokinases) are enzymes that catalyze the exchange of terminal phosphate between different nucleoside diphosphates (NDP) and triphosphates (NTP) in a reversible manner to produce nucleotide triphosphates. Many NDP serve as acceptor while NTP are donors of phosphate group.Glucose transporterGlucosylceramide beta-1,4-galactosyltransferase: Glucosylceramide beta-1,4-galactosyltransferase (, lactosylceramide synthase, uridine diphosphate-galactose:glucosyl ceramide beta 1-4 galactosyltransferase, UDP-Gal:glucosylceramide beta1->4galactosyltransferase, GalT-2, UDP-galactose:beta-D-glucosyl-(1<->1)-ceramide beta-1,4-galactosyltransferase) is an enzyme with system name UDP-alpha-D-galactose:beta-D-glucosyl-(1<->1)-ceramide 4-beta-D-galactosyltransferase. This enzyme catalyses the following chemical reactionLiver sinusoid: A liver sinusoid is a type of sinusoidal blood vessel (with fenestrated, discontinuous endothelium) that serves as a location for the oxygen-rich blood from the hepatic artery and the nutrient-rich blood from the portal vein.SIU SOM Histology GICis-acting replication element: Cis-acting replication elements brings together the 5' and 3' ends during replication of positive sense single stranded RNA viruses (for example Picornavirus, Flavivirus, coronavirus, togaviruses, Hepatitis C virus) and double stranded RNA viruses (for example rotavirus and reovirus).MannosamineChromatographic response function: Chromatographic response function, often abbreviated to CRF, is a coefficient which measures the quality of the separation in the result of a chromatography.Dimethylallyl pyrophosphateManganese deficiency (plant): Manganese (Mn) deficiency is a plant disorder that is often confused with, and occurs with, iron deficiency. Most common in poorly drained soils, also where organic matter levels are high.GlucosamineElectrophoresis (disambiguation): Electrophoresis is the motion of dispersed particles relative to a fluid under the influence of a spatially uniform electric field.Nucleoside-triphosphate-hexose-1-phosphate nucleotidyltransferase: Nucleoside-triphosphate-aldose-1-phosphate nucleotidyltransferase (, NDP hexose pyrophosphorylase, hexose 1-phosphate nucleotidyltransferase, hexose nucleotidylating enzyme, nucleoside diphosphohexose pyrophosphorylase, hexose-1-phosphate guanylyltransferase, GTP:alpha-D-hexose-1-phosphate guanylyltransferase, GDP hexose pyrophosphorylase, guanosine diphosphohexose pyrophosphorylase, NTP:hexose-1-phosphate nucleotidyltransferase) is an enzyme with system name NTP:alpha-D-aldose-1-phosphate nucleotidyltransferase. This enzyme catalyses the following chemical reactionDigitoninSpecificity constant: In the field of biochemistry, the specificity constant (also called kinetic efficiency or k_{cat}/K_{M}), is a measure of how efficiently an enzyme converts substrates into products. A comparison of specificity constants can also be used as a measure of the preference of an enzyme for different substrates (i.NTP binding site: An NTP binding site is a type of binding site found in nucleoside monophosphate (NMP) kinases, N can be adenosine or guanosine. A P-loop is one of the structural motifs common for nucleoside triphosphate (NTP) binding sites, it interacts with the bound nucleotide's phosphoryl groups.LisH domain: In molecular biology, the LisH domain (lis homology domain) is a protein domain found in a large number of eukaryotic proteins, from metazoa, fungi and plants that have a wide range of functions. The recently solved structure of the LisH domain in the N-terminal region of LIS1 depicted it as a novel dimerisation motif, and that other structural elements are likely to play an important role in dimerisation.Galactokinase deficiencyAlkylphenolMagnesium acetateIrinotecanLecithinase: Lecithinase is a type of phospholipase that acts upon lecithin.Alkaliphile: Alkaliphiles are a class of extremophilic microbes capable of survival in alkaline (pH roughly 8.5-11) environments, growing optimally around a pH of 10.Dimethylallyltranstransferase: Dimethylallyltranstransferase is an enzyme that converts dimethylallylpyrophosphate and isopentenyl pyrophosphate into farnesylpyrophosphate. It is also referred to as farnesylpyrophosphate synthase or farnesyldiphosphate synthase.PhenobarbitalGalactose-1-phosphate uridylyltransferase deficiencyCytidineColes PhillipsDNA binding site: DNA binding sites are a type of binding site found in DNA where other molecules may bind. DNA binding sites are distinct from other binding sites in that (1) they are part of a DNA sequence (e.Geranylgeranyl diphosphate reductase: Geranylgeranyl diphosphate reductase (, geranylgeranyl reductase, CHL P) is an enzyme with system name geranylgeranyl-diphosphate:NADP+ oxidoreductase. This enzyme catalises the following chemical reaction