Niveles de CK en la sangre – examen usado para medir la creatina kinasa, una [.. .] y aumento en los niveles de creatina quinasa (un indicador de daño [ ]. Prueba de quinasa creatina: análisis de sangre realizado para detectar niveles elevados de proteínas musculares o enzimas llamadas quinasa creatina (CK. Las medidas de la actividad total o de la isoenzima 2 (CKMM) de la creatina cinasa (CK) constituyen los marcadores biológicos más empleados de lesión.
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Allosteric regulation Cooperativity Enzyme inhibitor Enzyme activator. Apart from the two mitochondrial CK isoenzyme forms, that is, ubiquitous mtCK present in non-muscle tissues and sarcomeric mtCK present in sarcomeric musclequinasx are three cytosolic CK isoforms present in the cytosol, depending on the tissue.
Ornithine aminotransferase Ornithine decarboxylase Agmatinase.
Furthermore, the isoenzyme determination has been used extensively as an indication for myocardial damage in heart attacks. Saccharopine dehydrogenase Glutaryl-CoA dehydrogenase.
Translation of “creatina quinasa” in English
Quinxsa pros-kinase Protein-histidine tele-kinase Histidine kinase. From Wikipedia, the free encyclopedia. The mitochondrial creatine kinase CK m is present in the mitochondrial intermembrane space, where it regenerates phosphocreatine PCr from mitochondrially generated ATP and creatine Cr imported from the cytosol.
Theo Wallimann at the Biol. Ferritin Serum iron Transferrin saturation Total iron-binding capacity Transferrin Transferrin receptor.
Both mitochondrial CK isoforms are building highly symmetrical octameric structures with 4-fold symmetry. Mitochondrial membrane transport protein Mitochondrial permeability transition pore Mitochondrial carrier. This page was last edited on 17 Decemberat Creatine kinase Crystal structure of human brain-type creatine kinase with ADP and creatine.
Finally, high CK in the blood may be an indication of damage to CK-rich tissue, such as in rhabdomyolysismyocardial infarctionmyositis and myocarditis. Chemical pathology EC 2. ETH Zurich and by Dr. Clinically, creatine kinase is assayed in blood tests as a marker of damage of CK-rich tissue cgeatin as in myocardial infarction heart attackrhabdomyolysis severe muscle breakdownmuscular dystrophyautoimmune myositidesand acute kidney injury.
Histidine ammonia-lyase Urocanate hydratase Formiminotransferase cyclodeaminase. Guanidinoacetate N-methyltransferase Creatine kinase. Isoenzyme patterns differ in tissues. Essential amino acids are in Capitals.
The functional entity of the latter two mitochondrial CK isoforms is an octamer quihasa of four dimers each. In tissues and cells uqinasa consume ATP rapidly, especially skeletal musclebut also brain, photoreceptor cells of the retinahair cells of the inner earspermatozoa and smooth musclePCr serves as an energy reservoir for the qiunasa buffering and regeneration of ATP in situas well as for intracellular energy transport by the PCr shuttle or circuit.
The atomic structure of cytosolic brain-type BB-CK was solved at 1. Methionine adenosyltransferase Adenosylhomocysteinase regeneration of methionine: Views Read Edit View history.
This means creatine kinase in blood may be elevated in a wide range of clinical conditions including the use of medication such as statins ; endocrine disorders such as hypothyroidism ;  and skeletal muscle diseases and disorders including malignant hyperthermia and neuroleptic malignant syndrome.
creatina quinasa – Translation into English – examples Spanish | Reverso Context
Aspartate transaminase Glutamate dehydrogenase Pyruvate dehydrogenase complex. Cholesterol side-chain cleavage enzyme Steroid beta-hydroxylase Aldosterone synthase Frataxin. Adenylate kinase Creatine kinase.
Branched-chain amino acid aminotransferase Branched-chain alpha-keto acid dehydrogenase complex Enoyl-CoA hydratase 3-hydroxyisobutyryl-CoA hydrolase 3-hydroxyisobutyrate dehydrogenase Methylmalonate semialdehyde dehydrogenase. Retrieved from ” https: Cleveland Clinic Journal of Medicine.
In the cells, the “cytosolic” CK enzymes consist of two subunits, which can be either B brain type or M muscle type. The genes for these subunits are located on different chromosomes: Molecular and Cellular Biochemistry. B on 14q32 and M on 19q Carbamoyl phosphate synthetase I Ornithine transcarbamylase N-Acetylglutamate synthase. Branched-chain amino acid aminotransferase Branched-chain alpha-keto acid dehydrogenase complex 3-hydroxymethylbutyryl-CoA dehydrogenase. Ribose-phosphate diphosphokinase Thiamine diphosphokinase.
Carnitine palmitoyltransferase I Long-chain-fatty-acid—CoA ligase.