Species | Disruptability | Reference | Submitter | |
---|---|---|---|---|
P. berghei ANKA |
Possible |
PlasmoGEM (Barseq) | PlasmoGEM | |
P. falciparum 3D7 |
Refractory |
USF piggyBac screen (Insert. mut.) | USF PiggyBac Screen |
Species | Stage | Phenotype | Reference | Submitter |
---|---|---|---|---|
P. falciparum 3D7 | Asexual |
Cell cycle arrest |
https://www.biorxiv.org/content/10.1101/755439v1
(Conditional)
'Stalled during schizont development and failed to produce any merozoites so that there was no associated increase in parasitaemia' |
Theo Sanderson, Francis Crick Institute |
P. falciparum 3D7 | Asexual |
Refractory |
https://www.biorxiv.org/content/10.1101/755439v1 (Conditional) | Theo Sanderson, Francis Crick Institute |
Localization studies of UBA (E1) and UBC (E2). (A,B) IFA experiments, using different parasite stages, show that PfUBA1 and PfUBC localize mainly to the cytosol. (C) When co-immunostained with plasmepsin V (PMV), a Plasmodium ER membrane protein marker, there was noticeable overlap between the two proteins, suggesting UBA1 recruitment to the ER as well. Both UBC and UBA1 are mainly dispersed throughout the cytoplasm with small aggregations scattered throughout the parasite. UBA1 was co-immuno-stained with PMV, an ER membrane marker, showing noticeable overlap between the two proteins.Chung DW, Ponts N, Prudhomme J, Rodrigues EM, Le Roch KG. Characterization of the Ubiquitylating Components of the Human Malaria Parasite's Protein Degradation Pathway. PLoS One. 2012;7(8):e43477.
See original on MMPPlasmoDB | PVX_123920 |
GeneDB | PVX_123920 |
Malaria Metabolic Pathways | Localisation images Pathways mapped to |
Previous ID(s) | Pv123920 |
Orthologs | PBANKA_1440700 , PCHAS_1442700 , PF3D7_1225800 , PKNH_1445200 , PVP01_1444000 , PY17X_1443200 |
Google Scholar | Search for all mentions of this gene |