Kinetoplastid parasites compartmentalize the first seven enzymes of glycoly
sis in a peroxisome-like microbody, the glycosome. Genes encoding the most
abundant protein of the glycosomal membrane, GIM5, have been cloned and the
protein characterized. Two genes, GIM5A and GIM5B, encode 26 kDa proteins.
Although many microbody membrane proteins are conserved in evolution, the
only homologues of GIM5 in the available databases are from the closely rel
ated kinetoplastids Trypanosoma cruzi and Leishmania. The N- and C-termini
are conserved between the two genes, and between species, and are oriented
towards the cytosol. They are separated by a short loop that is located bet
ween two transmembrane domains and shows almost no sequence conservation. T
his suggests that the N- and C-terminal domains are more important for func
tion. GIM5 forms dimers in vivo. Overexpression of GIM5B inhibits growth, w
hereas depletion of GIM5 to below 10% of wild-type levels is very rapidly l
ethal. This novel organellar membrane protein is therefore essential for bl
oodstream trypanosome survival.