| 영문 | glycogen | 한글 | 글리코겐, 당원 |
|---|---|---|---|
| 설명 | 동물에서 탄수화물의 저장형태로 주로 간에 대부분이 저장되어 있고 근육에 조금 있다. 포도당으로 분해되어 이용된다. |
||
| GFFS | glycogen and fat-free solid |
|---|---|
| GSD | genetically significant dose; Gerstmann-Straussler disease; glutathione synthetase deficiency; glyco... |
| GSD-0 | glycogen storage disease-zero |
| GT1-GT10 | glycogen storage disease, types 1 to 10 |
| MLG | mesiolingual groove; mitochondrial lipid glycogen |
| PI3-kinases | Phosphatidylinositide 3-kinases |
|---|---|
| PI3-Kinases | Phosphoinositide 3-Kinases |
| GSK-3 beta | I)/glycogen synthase kinase-3 beta |
| GSK3 | Glycogen Synthase Kinase 3 |
| GS | Glycogen synthase |
| glycogen synthase | <enzyme> An enzyme of the transferase class that catalyses the reaction of udpglucose and (1,4-alpha-d-glucosyl)n to yield udp and 1,4-alpha-d-glucosyl)n+1. The reaction is highly regulated by allosteric effectors, by phosphorylation reactions, and by insulin. Chemical name: UDPglucose:glycogen 4-alpha-D-glucosyltransferase Registry number: EC 2.4.1.11 (12 Dec 1998) |
|---|---|
| glycogen synthase-d phosphatase | <enzyme> An enzyme that catalyses the conversion of phosphorylated, inactive glycogen synthase d to active dephosphoglycogen synthase I. Chemical name: (UDPglucose:glycogen 4-alpha-D-glucosyltransferase-D) phosphohydrolase Registry number: EC 3.1.3.42 (12 Dec 1998) |
| cyclic AMP-dependent protein kinases | <enzyme> A group of enzymes that are dependent on cyclic AMP and catalyze the phosphorylation of serine or threonine residues on proteins. Registry number: EC 2.7.10.- (12 Dec 1998) |
| cyclic GMP-dependent protein kinases | <enzyme> A group of enzymes that are dependent on cyclic GMP and catalyses the phosphorylation of serine or threonine residues of proteins. Registry number: EC 2.7.10.- (12 Dec 1998) |
| cyclic nucleotide-regulated protein kinases | <enzyme> A group of enzymes that catalyses the phosphorylation of serine or threonine residues of proteins and is dependent on cyclic nucleotides. Registry number: EC 2.7.10.- (12 Dec 1998) |
| cyclin-dependent kinases | Protein kinases that control cell cycle progression in all eukaryotes and require physical association with cyclins to achieve full enzymatic activity. Cyclin-dependent kinases are regulated by phosphorylation and dephosphorylation events. (12 Dec 1998) |
| protein kinases | <enzyme> A family of enzymes that catalyze the conversion of ATP and a protein to ADP and a phosphoprotein. Chemical name: ATP-protein phosphotransferase Registry number: EC 2.7.1.37 (12 Dec 1998) |
| protein-serine-threonine kinases | <enzyme> A group of enzymes that catalyses the phosphorylation of serine or threonine residues in proteins, with ATP or other nucleotides as phosphate donors. Registry number: EC 2.7.10 (12 Dec 1998) |
| src-family kinases | <enzyme> Family of non-receptor protein-tyrosine kinases homologous to src. They are closely related intracellular enzymes that participate in signal transduction pathways in a variety of haemopoietic cells and especially their surface receptors. Registry number: EC 2.7.1.- (12 Dec 1998) |
| brancher glycogen storage disease | Type of glycogen storage disease, due to deficiency of amylo-1,4-1,6-transglucosidase (brancher enzyme). Synonym: brancher deficiency glycogenosis, debrancher deficiency. (05 Mar 2000) |
| glycogen | <biochemistry> Branched polymer of D glucose (mostly _(1-4) linked, but some _(1-6) at branch points). Size range very variable, up to 10exp5 glucose units. Major short term storage polymer of animal cells and is particularly abundant in the liver and to a lesser extent in muscle. In the electron microscope glycogen has a characteristic asterisk or star appearance. (18 Nov 1997) |
| glycogen debranching enzyme system | 1,4-alpha-d-glucan-1,4-alpha-d-glucan 4-alpha-d-glucosyltransferase/dextrin 6 alpha-d-glucanohydrolase. An enzyme system having both 4-alpha-glucanotransferase (ec 2.4.1.25) and amylo-1,6-glucosidase (ec 3.2.1.33) activities. As a transferase it transfers a segment of a 1,4-alpha-d-glucan to a new 4-position in an acceptor, which may be glucose or another 1,4-alpha-d-glucan. As a glucosidase it catalyses the endohydrolysis of 1,6-alpha-d-glucoside linkages at points of branching in chains of 1,4-linked alpha-d-glucose residues. Amylo-1,6-glucosidase activity is deficient in glycogen storage disease type III. (12 Dec 1998) |
| glycogen granule | Glycogen occurring in cells as beta granule's which average about 300 A |
| glycogen phosphorylase | <enzyme> Enzyme that catalyses the sequential removal of glycosyl residues from glycogen to yield one glucose-1-phosphate per reaction. Its activity is controlled by phosphorylation (by phosphorylase kinase). (21 Jun 2000) |
| glycogen storage disease | <hepatology> A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalised storage of glycogen occurs, sometimes with prominent cardiac involvement. Synonym: glycogenosis (12 Sep 2002) |
Synonyms : Glycogen Synthase Kinase, Kinase, Glycogen Synthase, Kinases, Glycogen Synthase, Synthase Kinase, Glycogen
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|