Disruptability [+]

Species Disruptability Reference Submitter
P. falciparum 3D7
Refractory
USF piggyBac screen (Insert. mut.) USF PiggyBac Screen
P. berghei ANKA
Possible
PlasmoGEM (Barseq) PlasmoGEM

Mutant phenotypes [+]

Species Stage Phenotype Reference Submitter
P. berghei ANKA Asexual
No difference
PlasmoGEM (Barseq) PlasmoGEM

Imaging data (from Malaria Metabolic Pathways)

Localization of LipA–GFP fusion and LplA–GFP fusion constructs overexpressed in P. falciparum. A. The first N-terminal 339 nucleotides of the lipA gene were cloned in frame with green fluorescent protein (GFP). The peptide confers transit of GFP into an organelle distinct from the mitochondrion as shown by co-staining the parasites with MitoTracker CMX Ros. The figure demonstrates the morphological changes of the apicoplast throughout the erythrocytic cycle of the parasites. Phase: phase-contrast image MitoTracker: image. Merge: merge of phase-contrast, GFP and rhodamine channel. B. The first N-terminal 357 nucleotides of the lplA-GFP targets to the mitochondrion. The co-localization of GFP and MitoTracker fluorescence suggests that the LplA N-terminal extension represents mitochondrial targeting sequence. taken of mitochondrion using the rhodamine channel.Wrenger C, Müller S. The human malaria parasite Plasmodium falciparum has distinct organelle-specific lipoylation pathways. Mol Microbiol. 2004 53:103-13.

See original on MMP

More information

PlasmoDB PF3D7_1344600
GeneDB PF3D7_1344600
Malaria Metabolic Pathways Localisation images
Pathways mapped to
Previous ID(s) MAL13P1.220
Orthologs PBANKA_1357500 , PCHAS_1362100 , PKNH_1256700 , PVP01_1210200 , PVX_083125 , PY17X_1363200
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