Literature DB >> 3807949

Two high affinity nucleoside transporters in Leishmania donovani.

B Aronow, K Kaur, K McCartan, B Ullman.   

Abstract

A rapid sampling kinetic technique has been used to evaluate the nucleoside transport functions of Leishmania donovani. The results indicated that L. donovani promastigotes possessed two independent purine nucleoside transporters with nonoverlapping substrate specificity. The first transported inosine, guanosine, and their analogs, while the second carried adenosine, analogs of adenosine, and the pyrimidine nucleosides, uridine, cytidine, and thymidine. The apparent Km values of the two nucleoside permeases for their purine nucleoside substrates were extraordinarily low, in the micromolar range. The organisms were capable of concentrating purine nucleosides from the medium and converting them to the nucleotide level with great efficiency and rapidity. Inosine and adenosine transport could be distinguished by different sensitivities to sulfhydryl reagents, suggesting structural differences between the two transporters. Finally, the two nucleoside transport systems of L. donovani were virtually refractory to inhibition by 4-nitrobenzylthioinosine and dipyridamole, two potent inhibitors of nucleoside entry into mammalian cells.

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Year:  1987        PMID: 3807949     DOI: 10.1016/0166-6851(87)90066-1

Source DB:  PubMed          Journal:  Mol Biochem Parasitol        ISSN: 0166-6851            Impact factor:   1.759


  21 in total

1.  Point mutations in a nucleoside transporter gene from Leishmania donovani confer drug resistance and alter substrate selectivity.

Authors:  G Vasudevan; B Ullman; S M Landfear
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-15       Impact factor: 11.205

Review 2.  Nucleoside and nucleobase transporters in parasitic protozoa.

Authors:  Scott M Landfear; Buddy Ullman; Nicola S Carter; Marco A Sanchez
Journal:  Eukaryot Cell       Date:  2004-04

3.  Developmentally regulated gene from Leishmania encodes a putative membrane transport protein.

Authors:  B R Cairns; M W Collard; S M Landfear
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

4.  Leishmania mexicana amazonensis: plasma membrane adenine nucleotide translocator and chemotaxis.

Authors:  S Detke; R Elsabrouty
Journal:  Exp Parasitol       Date:  2007-10-22       Impact factor: 2.011

5.  Genetic selection for a highly functional cysteine-less membrane protein using site saturation mutagenesis.

Authors:  Cassandra S Arendt; Keirei Ri; Phillip A Yates; Buddy Ullman
Journal:  Anal Biochem       Date:  2007-03-30       Impact factor: 3.365

6.  Uptake of the antitrypanosomal drug 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine (MDL 73811) by the purine transport system of Trypanosoma brucei brucei.

Authors:  T L Byers; P Casara; A J Bitonti
Journal:  Biochem J       Date:  1992-05-01       Impact factor: 3.857

Review 7.  Pyrimidine metabolism in schistosomes: A comparison with other parasites and the search for potential chemotherapeutic targets.

Authors:  Mahmoud H El Kouni
Journal:  Comp Biochem Physiol B Biochem Mol Biol       Date:  2017-07-21       Impact factor: 2.231

8.  Genetic dissection of pyrimidine biosynthesis and salvage in Leishmania donovani.

Authors:  Zachary N Wilson; Caslin A Gilroy; Jan M Boitz; Buddy Ullman; Phillip A Yates
Journal:  J Biol Chem       Date:  2012-02-24       Impact factor: 5.157

9.  Cloning of Leishmania nucleoside transporter genes by rescue of a transport-deficient mutant.

Authors:  G Vasudevan; N S Carter; M E Drew; S M Beverley; M A Sanchez; A Seyfang; B Ullman; S M Landfear
Journal:  Proc Natl Acad Sci U S A       Date:  1998-08-18       Impact factor: 11.205

10.  Multidrug resistance in Leishmania donovani is conferred by amplification of a gene homologous to the mammalian mdr1 gene.

Authors:  D M Henderson; C D Sifri; M Rodgers; D F Wirth; N Hendrickson; B Ullman
Journal:  Mol Cell Biol       Date:  1992-06       Impact factor: 4.272

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