Disruptability [+]

Species Disruptability Reference Submitter
P. falciparum 3D7
26118996 Theo Sanderson, Wellcome Trust Sanger Institute

Mutant phenotypes [+]

Species Stage Phenotype Reference Submitter
P. berghei ANKA Asexual
PlasmoGEM (Barseq) Imported from PlasmoGEM
P. falciparum 3D7 Asexual
Invasion defect
26118996 (Conditional)
DD tag
Theo Sanderson, Wellcome Trust Sanger Institute

Imaging data (from Malaria Metabolic Pathways)

Stage-specific subcellular localization of PfFKBP35 and PfCnA proteins. Stages of parasite growth are indicated on the right. Both proteins (green) were probed with their primary antibody followed by FITC-conjugated secondary antibody. Nuclei (red) were stained with TO-PRO-3 iodide. All panels are super-impositions of the two stains, showing intracellular location of the proteins relative to the nucleus. Note that yellow or orange indicatesco-localization of green and red, signifying nuclear location of the protein, whereas green indicates cytoplasmic location. A significant amount of PfFKBP35 translocated to the nucleus as the rings differentiated into trophozoites and schizonts. PfCN, on the other hand, remained essentially in the cytoplasm when expressed. Kumar R, Adams B, Musiyenko A, Shulyayeva O, Barik S. The FK506-bindingprotein of the malaria parasite, Plasmodium falciparum, is a FK506-sensitive chaperone with FK506-independent calcineurin-inhibitory activity. Mol Biochem Parasitol. 2005 141(2):163-73. Copyright Elsevier

See original on MMP

More information

PlasmoDB PKNH_1230400
GeneDB PKNH_1230400
Malaria Metabolic Pathways Localisation images
Pathways mapped to
Previous ID(s) PK14_2322w, PKH_125460
Orthologs PBANKA_1315400 , PCHAS_1318700 , PF3D7_1451700 , PVP01_1255300 , PVX_117895 , PY17X_1319200
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