PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 2550078-5 1989 Ca2+ (2-20 mM) and glycerol (10-20%) increased the degree of crosslinking at pH 6.0 both in vesicular and in solubilized sarcoplasmic reticulum, presumably by promoting interactions between ATPase molecules; at pH 7.5 the effect of Ca2+ was less pronounced. Glycerol 19-27 dynein axonemal heavy chain 8 Homo sapiens 190-196 11725924-0 2001 Reduced activities of divalent cation activated ATP-ase and 5"-nucleotidase in glycerol induced acute renal failure. Glycerol 79-87 dynein axonemal heavy chain 8 Homo sapiens 48-55 1832831-3 1991 Ratio of ATPase or phosphatase activity and formation of phosphoenzyme intermediate was constant during purification after the first glycerol density gradient centrifugation. Glycerol 133-141 dynein axonemal heavy chain 8 Homo sapiens 9-15 2148684-5 1990 Glycerol gradient sedimentation showed that the purified ATPase sedimented at an s20,w of 7 S, and polyacrylamide gel electrophoresis under denaturing conditions reveals two polypeptides with relative molecular weights of 83,000 and 68,000. Glycerol 0-8 dynein axonemal heavy chain 8 Homo sapiens 57-63 1837235-5 1991 Glycerol and low temperature presumably reduce stacking by interfering with the interactions between the hydrophilic headgroups of Ca(2+)-ATPase molecules in adjacent lamellae, while not affecting or promoting the ordering of ATPase molecules within the individual sheets. Glycerol 0-8 dynein axonemal heavy chain 8 Homo sapiens 138-144 4031048-1 1985 A method for the continuous measurement of ATP hydrolysis (ATPase) by demembranated muscle fibres has been applied to isometrically held, glycerol-extracted flight muscle fibres from the water-bug Lethocerus, under conditions of high MgATP, neutral pH, and varying ionic strength, Ca2+ and extension. Glycerol 138-146 dynein axonemal heavy chain 8 Homo sapiens 59-65 2839505-3 1988 In this report we show that the ATPase remains associated with the factor upon glycerol gradient sedimentation. Glycerol 79-87 dynein axonemal heavy chain 8 Homo sapiens 32-38 2451665-7 1988 The stabilization of the ATPase activity in the presence of detergents is the combined effect of high Ca2+ (20 mM) and a relatively high glycerol concentration (20%). Glycerol 137-145 dynein axonemal heavy chain 8 Homo sapiens 25-31 2451665-8 1988 Ethylene glycol, glucose, sucrose, or myoinositol can substitute for glycerol with preservation of ATPase activity for several weeks in the presence of 20 mM Ca2+.Ca2+-induced association between ATPase molecules may be an essential requirement for preservation of enzymatic activity, both in intact sarcoplasmic reticulum and in solubilized preparations. Glycerol 69-77 dynein axonemal heavy chain 8 Homo sapiens 196-202 2966149-1 1988 The characteristics of glycerol-induced inhibition of the dynein ATPase extracted from Tetrahymena cilia were investigated. Glycerol 23-31 dynein axonemal heavy chain 8 Homo sapiens 65-71 2966149-2 1988 Fifty percent inhibition was observed at about 15% (v/v) glycerol with the 22S dynein Mg-ATPase. Glycerol 57-65 dynein axonemal heavy chain 8 Homo sapiens 89-95 2966149-4 1988 The glycerol-induced inhibition of the 22S dynein Mg-ATPase was not influenced by pH or by raising the ionic strength of the assay solution. Glycerol 4-12 dynein axonemal heavy chain 8 Homo sapiens 53-59 2966149-9 1988 Glycerol reduced the sensitivity of the dynein ATPase to the vanadate-induced inhibition. Glycerol 0-8 dynein axonemal heavy chain 8 Homo sapiens 47-53 2966149-11 1988 If it is assumed that the rate constants of the ATP hydrolysis step are not affected by glycerol, it may be implied that the phosphate release from the E.ADP.P1 intermediate was decelerated by glycerol and that the deceleration of the phosphate release paralleled the reduction of the overall ATPase activity over a wide range of glycerol concentration. Glycerol 193-201 dynein axonemal heavy chain 8 Homo sapiens 293-299 2966149-11 1988 If it is assumed that the rate constants of the ATP hydrolysis step are not affected by glycerol, it may be implied that the phosphate release from the E.ADP.P1 intermediate was decelerated by glycerol and that the deceleration of the phosphate release paralleled the reduction of the overall ATPase activity over a wide range of glycerol concentration. Glycerol 193-201 dynein axonemal heavy chain 8 Homo sapiens 293-299 3015211-10 1986 Progressive displacement of ATPase activity into three different peaks at 32%, 26% and 20% glycerol was found with increasing detergent concentrations. Glycerol 91-99 dynein axonemal heavy chain 8 Homo sapiens 28-34 2872216-2 1986 The reconstituted liposomes were then subjected to two additional rounds of glycerol density gradient centrifugation, which separate the H+-ATPase-bearing proteoliposomes from ATPase-free liposomes by virtue of their greater density. Glycerol 76-84 dynein axonemal heavy chain 8 Homo sapiens 140-146 6208191-6 1984 Glycerol velocity gradient analysis showed that p30-I sedimented as a 30-kDa species while the p30-II and its associated ATPase sedimented as a 60-kDa species. Glycerol 0-8 dynein axonemal heavy chain 8 Homo sapiens 121-127 6461976-2 1982 Delipidation of the Ca2+-ATPase of sarcoplasmic reticulum membranes by gel chromatography employing ionic detergents (cholate, deoxycholate and mixtures of both) in the presence of glycerol has been studied with respect to residual phospholipids and ATPase activities. Glycerol 181-189 dynein axonemal heavy chain 8 Homo sapiens 250-256 6228071-7 1983 Glycerol (10-30%, v/v) slightly enhanced the ATPase activity maximum and reduced the rate of inactivation essentially only by decreasing the DTNB modification rate. Glycerol 0-8 dynein axonemal heavy chain 8 Homo sapiens 45-51 152310-0 1978 Acceleration of the ATPase activity of glycerol-treated muscle fibers by repeated stretch-release cycles. Glycerol 39-47 dynein axonemal heavy chain 8 Homo sapiens 20-26 159296-1 1979 During the inactivation of the nucleotide-free F1-ATPase at pH 7.0, by p-fluorosulfonyl[14C]benzoyl-5"-adenosine ([14C]FSBA) in the presence of 20% glycerol, about 4.5 g atoms of 14C are incorporated/350,000 g of enzyme. Glycerol 148-156 dynein axonemal heavy chain 8 Homo sapiens 50-56 220891-0 1979 A fluorimetric method for continuously assaying ATPase: application to small specimens of glycerol-extracted muscle fibers. Glycerol 90-98 dynein axonemal heavy chain 8 Homo sapiens 48-54 150416-3 1978 Inactivations of the ATPase with p-fluorosulfonyl[14C]benzoyl-5"-adenosine were most efficiently accomplished with the nucleotide-free enzyme at pH 7.0, in a buffer containing 20% glycerol. Glycerol 180-188 dynein axonemal heavy chain 8 Homo sapiens 21-27 4258110-0 1970 Correlation between tension and ATPase activity in glycerol treated fibers. Glycerol 51-59 dynein axonemal heavy chain 8 Homo sapiens 32-38 140874-1 1977 The Ca2+-ATPase of sarcoplasmic reticulum can be reversibly delipidated by precipitation with polyethyleneglycol in the presence of deoxycholate and glycerol to as low as 4 mol of phospholipid/mol of enzyme polypeptide and can then be reactivated to 90% of its original ATPase activity by the addition of phosphatidylcholine. Glycerol 149-157 dynein axonemal heavy chain 8 Homo sapiens 9-15 145242-9 1977 Glycerol inhibited and salts enhanced the cold inactivation of membrane-bound F1-ATPase. Glycerol 0-8 dynein axonemal heavy chain 8 Homo sapiens 81-87 4236957-0 1969 The coupling of poweroutput and myofibrillar ATPase activity in glycerol-extracted insect fibrillar muscle at varying amplitude of ATP-driven oscillation. Glycerol 64-72 dynein axonemal heavy chain 8 Homo sapiens 45-51