Proteomes · Leishmania infantum
- Proteome IDUP000008153
- StatusReference proteome
- Number of entries
- Gene count
- Taxonomy | StrainLeishmania infantum | JPCM5
- Genome assembly and annotation
- Genome representationFull
- Completeness (CPD)Standard
- BUSCOSingleDuplicatedFragmentedMissingn:130 · euglenozoa_odb10C:100% (S:100% D:0%) F:0% M:0%
Description
Leishmania is a genus of trypanosomatid parasites that are intracellular pathogens of the immune system and are the causative agents of the disease Leishmaniasis, which is an infectious disease that is transmitted by the bite of certain species of sand fly.
Over 20 Leishmania species can infect humans and cause a spectrum of diseases. The symptoms range from disfiguring cutaneous and mucocutaneous lesions to visceral disease affecting the hematopoietic organs. Leishmaniasis affects the populations of 88 tropical and subtropical countries worldwide, and there is currently no vaccine and few effective drugs for it.
Leishmania infantum is an Old World pathogen, being present in Africa, Europe and Asia, and is the primary cause of visceral leishmaniasis in the Mediterranean region.
The reference proteome of Leishmania infantum is derived from the genome sequence published in 2007. The size of the haploid genome is 32Mb consisting 36 chromosomes.
Components
Component name | Genome accession(s) | Protein count | |
---|---|---|---|
Chromosome 1 | FR796433 | 81 | |
Chromosome 2 | FR796434 | 73 | |
Chromosome 3 | FR796435 | 95 | |
Chromosome 4 | FR796436 | 125 | |
Chromosome 5 | FR796437 | 120 | |
Chromosome 6 | FR796438 | 133 | |
Chromosome 7 | FR796439 | 128 | |
Chromosome 8 | FR796440 | 117 | |
Chromosome 9 | FR796441 | 160 | |
Chromosome 10 | FR796442 | 140 | |
Chromosome 11 | FR796443 | 132 | |
Chromosome 12 | FR796444 | 113 | |
Chromosome 13 | FR796445 | 162 | |
Chromosome 14 | FR796446 | 153 | |
Chromosome 15 | FR796447 | 158 | |
Chromosome 16 | FR796448 | 172 | |
Chromosome 17 | FR796449 | 155 | |
Chromosome 18 | FR796450 | 166 | |
Chromosome 19 | FR796451 | 168 | |
Chromosome 20 | FR796452 | 176 | |
Chromosome 21 | FR796453 | 222 | |
Chromosome 22 | FR796454 | 162 | |
Chromosome 23 | FR796455 | 191 | |
Chromosome 24 | FR796456 | 239 | |
Chromosome 25 | FR796457 | 253 | |
Chromosome 26 | FR796458 | 262 | |
Chromosome 27 | FR796459 | 260 | |
Chromosome 28 | FR796460 | 316 | |
Chromosome 29 | FR796461 | 292 | |
Chromosome 30 | FR796462 | 371 | |
Chromosome 31 | FR796463 | 324 | |
Chromosome 32 | FR796464 | 405 | |
Chromosome 33 | FR796465 | 338 | |
Chromosome 34 | FR796466 | 422 | |
Chromosome 35 | FR796467 | 531 | |
Chromosome 36 | FR796468 | 725 | |
Unassembled WGS sequence | CACT01000000 | 40 |