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Results 1 - 10 of 16 > >>
EC Number Application Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 2.7.3.2biotechnology stability of immobilized enzyme 642382
Display the word mapDisplay the reaction diagram Show all sequences 2.7.3.2biotechnology use as biomarker of sperm cell membrane degradation 642426
Display the word mapDisplay the reaction diagram Show all sequences 2.7.3.2diagnostics enzyme is clinically important as an indicator of myocardial and skeletal muscle disorders and for the diagnosis of acute myocardial infarction 661528
Display the word mapDisplay the reaction diagram Show all sequences 2.7.3.2medicine changes in the kinetics of the creatine kinase shuttle are sensitive markers of cardiac energetics 762027
Display the word mapDisplay the reaction diagram Show all sequences 2.7.3.2medicine enzyme properties relevant for analysis 642388
Display the word mapDisplay the reaction diagram Show all sequences 2.7.3.2medicine ethylmalonic acid accumulates in patients affected by short-chain acyl-CoA dehydrogenase deficiency and other diseases. Ethylmalonic acid inhibits the activity of respiratory chain complexes and also inhibits creatine kinase at concentrations o 1 mM and 5 mM and may therefore compromise energy metabolism in skeletal muscle 675781
Display the word mapDisplay the reaction diagram Show all sequences 2.7.3.2medicine increased troponin I levels in the presence of rest pain and normal creatine kinase is not a spurious finding, but may actually be a marker of advanced coronary artery disease. However, some of these patients may also have nonsignificant coronary artery disease 688203
Display the word mapDisplay the reaction diagram Show all sequences 2.7.3.2medicine levels of both free and protein-bound 4-hydroxy-2-nonenal are increased in alzheimer’s disease brain. 4-Hydroxy-2-nonenal inhibitis creatine kinase dose-dependently and forms adducts with specific amino acids including the active site residues H66, H191, C283, and H296 673067
Display the word mapDisplay the reaction diagram Show all sequences 2.7.3.2medicine mutations in the dysferlin gene cause several muscular dystrophy phenotypes including limb girdle 2B, Miyoshi myopathy, and distal anterior compartment myopathy. These disorders are characterized by autosomal recessive inheritance, early adult onset, and elevated levels of serum creatine kinase 689192
Display the word mapDisplay the reaction diagram Show all sequences 2.7.3.2medicine neurotoxicitiy of L-arginine in hyperargininemia may in part be due to inhibition of creatine kinase 675783
Results 1 - 10 of 16 > >>