Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:3.6.3.1 (Mg2+-ATPase)
 1,484 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The total ATPase activity of the rabbit skeletal muscle nuclei was established to be a sum of activities of two ATPases--Mg2+ and Mg2+, Ca2+-ATPases. The latter composes 50% of total ATPase activity for skeletal muscles nuclei of the normal rabbits and 30% for skeletal muscles nuclei of the rabbits with muscular dystrophy. Mg+, Ca2+-ATPase of the skeletal muscle nuclei is activated by calcium ions within a range of 10(-6)--10(-4) M and is inhibited with its concentration of 0.5-10(-3) M and higher. Sodium and potassium ions activate Mg2+, Ca2+-ATPase. Inhibition of Mg2+-ATPase is observed for the skeletal muscle nuclei of the rabbits in norm with the presence of 80 mM of Na+ and 70 mM of K+ in the incubation medium. Under experimental muscular dystrophy such an effect is not observed in connection with the fact that the concentration of monovalent cations in the incubation medium does not exceed 60 mM. The ATPase activity in nuclei of the rabbit skeletal muscles may be also manifested in the presence of Mn2+ greater than Ca2+ greater than Ba2+. A problem is under discussion as to substitution of ions Mg2+ by ions Mn2+, Ca2+, Ba2+ in manifestation of the Mg2+ATPase activity for the skeletal muscle nuclei of the normal rabbits and of those with experimental dystrophy.
 ...
PMID:[Mg 2+, Ca 2+-ATPase of skeletal muscle nuclei in normal rabbits and in rabbits with experimental muscular dystrophy]. 12 61

The properties and localization of ATPase system in nuclei of skeletal muscle of normal rabbit and of those with experimental muscle dystrophy were studied by electron cytochemistry. The product of cytochemical reaction of ATP hydrolysis, which is a marker of ATPase activity localization in nuclear ultrastructures, was detected on the nuclear membrane, in chromatin and in the nucleolus, ATPase activity in the nuclei was detected in the presence of both, Mg2+ and Ca2+. Addition to the incubation medium, originally containing Mg2+, Na+ and K+, resulted in an increased formation of the product reaction in all the nuclear ultrastructures in both in the norm and under experimental muscle dystrophy. However, specific inhibitor of Mg2+, Na+, K+-ATPase--ouabain--suggests the absence in the nuclei of skeletal muscles of rabbit of transport ATPase working in the "Na-pump" system. The results of experiments with a specific complex of Ca2+--EGTA allow to suppose that Mg2+, Ca2+-ATPase of skeletal muscle nuclei of normal rabbits is localized in the nucleoplasm, whereas Mg2+-ATPase is found on the nuclear membrane. Using EGTA we failed to detected the localization of Mg2+, Ca2+-ATPase in nuclear ultrastructures upon experimental muscular dystrophy.
 ...
PMID:[Electron-cytochemical study of the localization and properties of ATPases in the isolated nuclei of rabbit skeletal muscle under normal conditions and in experimental muscular dystrophy]. 14 28

The cation-stimulated ATPase activities of erythrocyte membranes from patients with myotonic muscular dystrophy (MyD) were compared with the activities in age- and sex-matched controls. The enzymes included ouabain-sensitive ATPase, Mg2+-ATPase and Ca2+ + Mg2+-ATPase. Sampling and processing of the materials from patients with MyD and controls were simultaneously done in each experiment. The enzyme activities were varied with or without EGTA in the reaction medium, or with different temperatures for membrane storage, but no significant differences between MyD and control were observed in any conditions. The present study indicates no specific abnormality of the cation-stimulated ATPase activities of erythrocyte membranes in MyD.
 ...
PMID:Erythrocyte membrane cation-stimulated ATPase activities in myotonic muscular dystrophy. 612 Feb 17

The activity of [Na+ + K+] Mg2+-ATPase of muscle surface membrane was investigated in 20 cases of the Duchenne type of progressive muscular dystrophy; it was found to be diminished and to have a changed reactivity to ouabain. There was nothing like it in cases of limb-girdle dystrophy and neurogenic muscular atrophies investigated for the purpose of comparisons, whereas in some cases of myotonic dystrophy and myotonia congenita the activity of the ATPase was indeed depressed, but the response to ouabain invariably remained normal.
 ...
PMID:[Na+ + K+] Mg2+-ATPase of muscle plasma membranes in Duchenne muscular dystrophy. 625 58