PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 2549975-1 1989 Changes in 5"-nucleotidase activity were calculated on the basis of alterations in ATP, ADP, phosphocreatine, Pi, Mg2+, IMP and AMP, determined by using 31P n.m.r. Inosine Monophosphate 120-123 5' nucleotidase, ecto Rattus norvegicus 11-26 2537081-3 1989 Moreover, in the presence of MgCl2, NaCl and IMP, purified rat liver 5"-nucleotidase catalyzed the phosphorylation of c3Ado to 3-deazaadenosine 5"-monophosphate (c3AMP). Inosine Monophosphate 45-48 5' nucleotidase, ecto Rattus norvegicus 69-84 2844163-2 1988 A 5"-nucleotidase with a strong preference for AMP over IMP was characterized in homogenates and subcellular fractions of pigeon heart by using concentrations of ATP, ADP and AMP which mimicked those present in the ischaemic tissue. Inosine Monophosphate 56-59 5' nucleotidase, ecto Rattus norvegicus 2-17 2830790-4 1988 It exhibits phosphatase activity toward 5"-AMP, 5"-IMP, and 5"-GMP, but not toward 2"- and 3"-AMP and corresponds therefore to a 5"-nucleotidase. Inosine Monophosphate 48-54 5' nucleotidase, ecto Rattus norvegicus 129-144 16369729-8 2006 The activity of ecto-5"-nucleotidase increased 2-fold in diabetic cells resulting in a rise of the activity ratio of ecto-5"-nucleotidase/adenosine deaminase from 28 to 56.These results indicate that in rat cardiomyocytes diabetes alters activities of adenosine metabolizing enzymes in such a way that conversion of AMP to IMP is favored in the cytosolic compartment, whereas the capability to produce adenosine extracellularly is increased. Inosine Monophosphate 323-326 5' nucleotidase, ecto Rattus norvegicus 16-36 16369729-8 2006 The activity of ecto-5"-nucleotidase increased 2-fold in diabetic cells resulting in a rise of the activity ratio of ecto-5"-nucleotidase/adenosine deaminase from 28 to 56.These results indicate that in rat cardiomyocytes diabetes alters activities of adenosine metabolizing enzymes in such a way that conversion of AMP to IMP is favored in the cytosolic compartment, whereas the capability to produce adenosine extracellularly is increased. Inosine Monophosphate 323-326 5' nucleotidase, ecto Rattus norvegicus 117-137 12785725-6 2003 In the presence of ATP, which acts both as an activator of IMP-GMP-specific 5"-nucleotidase and as substrate of nucleoside mono- and di-phosphokinases, no IDP and ITP are formed. Inosine Monophosphate 59-62 5' nucleotidase, ecto Rattus norvegicus 76-91 3017317-1 1986 The rate of hydrolysis of IMP (0.5 mM) by cytosol 5"-nucleotidase from Artemia embryos was increased up to 7-fold by concentrations of around 10 microM diadenosine tetraphosphate (Ap4A). Inosine Monophosphate 26-29 5' nucleotidase, ecto Rattus norvegicus 50-65 7082301-17 1982 The modifications of these effectors can also explain the increased inhibition of the cytoplasmic 5"-nucleotidase, shown by the accumulation of IMP in the absence of coformycin, in hepatocytes from starved rats. Inosine Monophosphate 144-147 5' nucleotidase, ecto Rattus norvegicus 98-113 622078-8 1978 However, several findings indicated that the In was derived from IMP by catabolism by 5"-nucleotidase (NTase): (1) IMP decreased as In increased and (2) the inhibitors of NTase, adenosine monophosphate and thymidine triphosphate, reduced the generation of In by over 90% without inhibiting purine nucleoside phosphorylase. Inosine Monophosphate 65-68 5' nucleotidase, ecto Rattus norvegicus 86-101 622078-8 1978 However, several findings indicated that the In was derived from IMP by catabolism by 5"-nucleotidase (NTase): (1) IMP decreased as In increased and (2) the inhibitors of NTase, adenosine monophosphate and thymidine triphosphate, reduced the generation of In by over 90% without inhibiting purine nucleoside phosphorylase. Inosine Monophosphate 65-68 5' nucleotidase, ecto Rattus norvegicus 103-108 622078-8 1978 However, several findings indicated that the In was derived from IMP by catabolism by 5"-nucleotidase (NTase): (1) IMP decreased as In increased and (2) the inhibitors of NTase, adenosine monophosphate and thymidine triphosphate, reduced the generation of In by over 90% without inhibiting purine nucleoside phosphorylase. Inosine Monophosphate 65-68 5' nucleotidase, ecto Rattus norvegicus 171-176 622078-8 1978 However, several findings indicated that the In was derived from IMP by catabolism by 5"-nucleotidase (NTase): (1) IMP decreased as In increased and (2) the inhibitors of NTase, adenosine monophosphate and thymidine triphosphate, reduced the generation of In by over 90% without inhibiting purine nucleoside phosphorylase. Inosine Monophosphate 115-118 5' nucleotidase, ecto Rattus norvegicus 86-101 622078-8 1978 However, several findings indicated that the In was derived from IMP by catabolism by 5"-nucleotidase (NTase): (1) IMP decreased as In increased and (2) the inhibitors of NTase, adenosine monophosphate and thymidine triphosphate, reduced the generation of In by over 90% without inhibiting purine nucleoside phosphorylase. Inosine Monophosphate 115-118 5' nucleotidase, ecto Rattus norvegicus 103-108 622078-8 1978 However, several findings indicated that the In was derived from IMP by catabolism by 5"-nucleotidase (NTase): (1) IMP decreased as In increased and (2) the inhibitors of NTase, adenosine monophosphate and thymidine triphosphate, reduced the generation of In by over 90% without inhibiting purine nucleoside phosphorylase. Inosine Monophosphate 115-118 5' nucleotidase, ecto Rattus norvegicus 171-176 1996974-11 1991 Decavanadate increased the affinity of the soluble 5"-nucleotidase for 5"-IMP. Inosine Monophosphate 71-77 5' nucleotidase, ecto Rattus norvegicus 51-66