| Species | Disruptability | Reference | Submitter | |
|---|---|---|---|---|
| P. yoelii yoelii 17X |
Refractory |
RMgm-4810 | Imported from RMgmDB | |
| P. berghei ANKA |
Refractory |
RMgm-1400 | Imported from RMgmDB | |
| P. berghei ANKA |
Refractory |
RMgm-323 | Imported from RMgmDB | |
| P. berghei ANKA |
Refractory |
RMgm-324 | Imported from RMgmDB | |
| P. falciparum 3D7 |
Refractory |
18452584 | Theo Sanderson, Wellcome Trust Sanger Institute | |
| P. falciparum 3D7 |
Possible |
USF piggyBac screen (Insert. mut.) | USF PiggyBac Screen | |
| Species | Stage | Phenotype | Reference | Submitter |
|---|---|---|---|---|
| P. berghei ANKA | Asexual |
Attenuated |
PlasmoGEM (Barseq) | PlasmoGEM |
| P. falciparum 3D7 | Asexual |
Egress defect |
33500341 DiCre system \'GCα-null parasites cannot synthesize cGMP or mobilize calcium, a cGMP-dependent protein kinase (PKG)-driven requirement for egress. Using chemical complementation with a cGMP analogue and point mutagenesis of a crucial conserved residue within the P4-ATPase domain, we show that P4-ATPase activity is upstream of and linked to cGMP synthesis. Collectively, our results demonstrate that GCα is a critical regulator of PKG and that its associated P4-ATPase domain plays a primary role in generating cGMP for merozoite egress.\' |
Theo Sanderson, Francis Crick Institute |
| PlasmoDB | PY17X_0911700 |
| GeneDB | PY17X_0911700 |
| Malaria Metabolic Pathways | Localisation images Pathways mapped to |
| Previous ID(s) | null |
| Orthologs | PBANKA_0910300 , PCHAS_0711600 , PF3D7_1138400 , PKNH_0936600 , PVP01_0939400 , PVX_092535 |
| Google Scholar | Search for all mentions of this gene |