Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jürg M. Sommer"'
Publikováno v:
Molecular and Biochemical Parasitology. 76:83-89
A procyclic Trypanosoma brucei double-knockout mutant lacking the ornithine decarboxylase (ODC) gene was transfected with a T. brucei genomic library in the expression vector pTSO-HYG4, which utilizes the PARP promoter and replicates extrachromosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c3ffdaf6ba3c37a9413445d195365ec
https://doi.org/10.1016/0166-6851(95)02543-x
https://doi.org/10.1016/0166-6851(95)02543-x
Publikováno v:
Molecular and Cellular Biology. 10:4545-4554
Glycosomes are microbody organelles found in kinetoplastida, where they serve to compartmentalize the enzymes of the glycolytic pathway. In order to identify the mechanism by which these enzymes are targeted to the glycosome, we have modified the in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::295dbf398119c46fb634c768c5c8f2d0
https://doi.org/10.1128/mcb.10.9.4545
https://doi.org/10.1128/mcb.10.9.4545
Publikováno v:
Experimental parasitology. 85(1)
Among the microbodies found in eukaryotes are the glycosomes of Trypanosoma brucei, thought to be closely related to peroxisomes. Two types of targeting signals for glycosomes have been identified thus far: type 1 at the C-terminus and type 2 at the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b3949f9cdf18a2f0f6cf79dcbdb727d
https://pubmed.ncbi.nlm.nih.gov/9024198
https://pubmed.ncbi.nlm.nih.gov/9024198
Publikováno v:
Molecular and biochemical parasitology. 78(1-2)
Giardia lamblia is one of the most ancient eukaryotes identified to date. It lacks de novo purine biosynthesis and is thought to rely solely on the functions of two salvage enzymes, adenine and guanine phosphoribosyltransferases (APRTase and GPRTase)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::763216bf7412a72eb0efcd69e81f5850
https://pubmed.ncbi.nlm.nih.gov/8813688
https://pubmed.ncbi.nlm.nih.gov/8813688
Publikováno v:
FEBS letters. 350(1)
Import of proteins into the glycosomes of T. brucei resembles the peroxisomal protein import in that C-terminal SKL-like tripeptide sequences can function as targeting signals. Many of the glycosomal proteins do not, however, possess such C-terminal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2a0e3b2230b835301afc9059a13239d
https://pubmed.ncbi.nlm.nih.gov/7914876
https://pubmed.ncbi.nlm.nih.gov/7914876
Autor:
Chao Wang, Jürg M. Sommer
Publikováno v:
Annual review of microbiology. 48
Glycosomes are microbodies found in protozoa belonging to the order Kinetoplastida. These highly specialized organelles compartmentalize most of the glycolytic enzymes normally located in the cytosol of other eukaryotic cells. The recent success in e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c143e2ecf96157ffdb6887e2931340d0
https://pubmed.ncbi.nlm.nih.gov/7826002
https://pubmed.ncbi.nlm.nih.gov/7826002
Publikováno v:
FEBS letters. 316(1)
Glycosomal phosphoglycerate kinase (gPGK) of Trypanosoma brucei differs from the cytoplasmic isozyme (cPGK) in its higher isoelectric point characterized by clusters of positive charges along the polypeptide chain, and a 20 amino acid C-terminal exte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b253753ae95631d7b5807d9a5de44f3
https://pubmed.ncbi.nlm.nih.gov/8422938
https://pubmed.ncbi.nlm.nih.gov/8422938
Publikováno v:
Molecular and cellular biology. 10(9)
Glycosomes are microbody organelles found in kinetoplastida, where they serve to compartmentalize the enzymes of the glycolytic pathway. In order to identify the mechanism by which these enzymes are targeted to the glycosome, we have modified the in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83b4d836c94c600943591f73094e8e56
https://pubmed.ncbi.nlm.nih.gov/2388617
https://pubmed.ncbi.nlm.nih.gov/2388617
Publikováno v:
Human Gene Therapy; 7/01/2004, Vol. 15 Issue 7, p709-715, 7p