Leishmania infantum JPCM5 genome chromosome 12.
Eukaryota; Euglenozoa; Kinetoplastida; Trypanosomatidae; Leishmaniinae; Leishmania.
Chromosome and gene copy number variation allow major structural change between species and strains of Leishmania
Comparative genomic analysis of three Leishmania species that cause diverse human disease
Submitted (16-JUL-2015) National Center for Biotechnology Information, NIH, Bethesda, MD 20894, USA
Submitted (24-JAN-2011) to the INSDC. Aslett M., Pathogen Sequencing Unit, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, Cambridgeshire, CB10 1SA, UNITED KINGDOM
PROVISIONAL REFSEQ: This record has not yet been subject to final\nNCBI review. The reference sequence is identical to FR796444.\nOn Jul 14, 2011 this sequence version replaced gi:146080474.\nData release policy http://www.sanger.ac.uk/legal/#t_2.
putative translation initiation factor EIF-2b alpha subunit
putative cysteine peptidase, Clan CA, family C19
putative proteasome regulatory ATPase subunittcc1l8.3
serine/threonine protein phosphatase-like protein
putative NADH:flavin oxidoreductase/NADH oxidase
metallo-peptidase, Clan MA(E), Family M1
puromycin-sensitive aminopeptidase-like protein
arginine N-methyltransferase-like protein