A Purine Nucleoside Hydrolase from Trypanosoma Gambiense, Purification and Properties
Overview
Tropical Medicine
Authors
Affiliations
A purine nucleoside hydrolase from Trypanosoma gambiense was purified 160-fold. Preferred substrates of the reaction were adenosine, inosine and guanosine with a maximum of activity at pH 5.4. Competitive inhibitors of the adenosine hydrolysis were dimethylallyl adenosine, 6-methylmercaptopurine riboside, tubercidin, formycin B, 6-mercaptopurine riboside and deoxyadenosine. A metabolic scheme of adenosine nomophosphate salvage synthesis is discussed.
Structure, Oligomerization and Activity Modulation in N-Ribohydrolases.
Degano M Int J Mol Sci. 2022; 23(5).
PMID: 35269719 PMC: 8910321. DOI: 10.3390/ijms23052576.
Enzymatic Transition States and Drug Design.
Schramm V Chem Rev. 2018; 118(22):11194-11258.
PMID: 30335982 PMC: 6615489. DOI: 10.1021/acs.chemrev.8b00369.
Guranowski A Plant Physiol. 1982; 70(2):344-9.
PMID: 16662492 PMC: 1067146. DOI: 10.1104/pp.70.2.344.
Allen T, Ullman B Nucleic Acids Res. 1993; 21(23):5431-8.
PMID: 8265360 PMC: 310582. DOI: 10.1093/nar/21.23.5431.
Purine metabolism in the protozoan parasite Eimeria tenella.
Wang C, Simashkevich P Proc Natl Acad Sci U S A. 1981; 78(11):6618-22.
PMID: 6273876 PMC: 349100. DOI: 10.1073/pnas.78.11.6618.