About Gene List

PF3D7_0215600 (GET2)

Genome location: Pf3D7_02_v3:642,807..644,902(-)

Genome classification: Core

Function and Localization

Product Description: Golgi to ER traffic protein 2

SignalP Peptide: N/A

# Transmembrane Domains: 3

EC Numbers: None

Curated GO (PlasmoDB):

Type GO Term Name
Function GO:0005515 protein binding

Expression by stage (LR - Le Roch et al., and MCA - Malaria Cell Atlas):

Stage LR class MCA mean MCA prop. zeros
Sporozoite possibly expressed N/A N/A
Ring expressed 0.22 0.89
Trophozoite expressed 0.39 0.76
Schizont expressed 0.11 0.93
Gametocyte expressed 0.33 0.80

More info:

Resistome Mutations

Old (Pf3D7v3) Gene ID: PF3D7_0215600

Resistome Missense Mutations: M364I

Resistome Compounds with Missense Mutations: Suloctidil

Resistome # Samples with Disruptive Mutations: 1 (1 missense, 1 "interesting" missense)

Essentiality (ABS)

Zhang Phenotype: Non - Mutable in CDS

MIS: 0.539 | MFS: -2.467 | #Insertions: 0

PlasmoGEM Phenotype: Slow (Pb ortholog: PBANKA_1212200)

  • Relative Growth Rate: 0.66 ± 0.09
  • Confidence: 6.15

RMgmDB ABS Phenotype: N/A

More info: PhenoPlasm Link

Binding Evidence

AlphaFill Uniprot ID: O96235

"Best" AlphaFill ligand hit: No AlphaFill hits

No associated EC numbers

No evidence of orthology to BindingDB entries

Orthology Information

Ortholog Group (OrthoMCL): OG6_130353

No human ortholog(s)

Genetic Variation

MalariaGEN Pf7 (worldwide samples) # unique SNV/indels:

Homozygous genotype calls only

variant type common rare doubleton singleton
synonymous 3 13 9 14
disruptive 27 59 18 84
missense 17 41 12 59

Any inclusion in genotype call

variant type common rare doubleton singleton
synonymous 7 24 6 18
disruptive 54 129 53 134
missense 27 87 35 66

PlasmoDB Total SNPs: 110

Non-coding: 30 | Synonymous: 42 | Nonsynonymous: 38 | Stop Codon: 0

Protein Information

Protein Length: 403 | Molecular Weight (kDa): 48.274

UniProt ID(s): O96235

PDB ID(s): None

Isoelectric Point: 7.29

Protein Domain Annotations:

Source Family ID Description
InterPro N/A N/A
PFam N/A N/A
Superfamily N/A N/A

Associated Publications

PMID Title Authors DOI/Link
9804551 Chromosome 2 sequence of the human malaria parasite Plasmodium falciparum. Gardner MJ, Tettelin H, ..., Hoffman SL 10.1126/science.282.5391.1126
12368864 Genome sequence of the human malaria parasite Plasmodium falciparum. Gardner MJ, Hall N, ..., Barrell B 10.1038/nature01097
16267556 A protein interaction network of the malaria parasite Plasmodium falciparum. LaCount DJ, Vignali M, ..., Hughes RE 10.1038/nature04104
34780541 A conserved guided entry of tail-anchored pathway is involved in the traffickingof a subset of membrane proteins in Plasmodium falciparum. Kumar T, Maitra S, Rahman A, Bhattacharjee S 10.1371/journal.ppat.1009595
37882342 Proteome-wide abundance profiling of yeast deletion strains for GET pathwaymembers using sample multiplexing Gygi JS, Liu X, Levi BP, Paulo JA 10.1002/pmic.202300303
29661846 The GET pathway can increase the risk of mitochondrial outer membrane proteins tobe mistargeted to the ER Vitali DG, Sinzel M, ..., Rapaport D 10.1242/jcs.211110
37286562 The GET pathway is a major bottleneck for maintaining proteostasis inSaccharomyces cerevisiae Josefson R, Kumar N, ..., Nystrom T 10.1038/s41598-023-35666-8
35231030 The ER membrane complex (EMC) can functionally replace the Oxa1 insertase inmitochondria Gungor B, Flohr T, Garg SG, Herrmann JM 10.1371/journal.pbio.3001380
33443185 Endoplasmic reticulum membrane receptors of the GET pathway are conservedthroughout eukaryotes Asseck LY, Mehlhorn DG, ..., Grefen C 10.1073/pnas.2017636118
37963916 The GET insertase exhibits conformational plasticity and induces membranethinning McDowell MA, Heimes M, ..., Sinning I 10.1038/s41467-023-42867-2
32910895 Structural Basis of Tail-Anchored Membrane Protein Biogenesis by the GETInsertase Complex McDowell MA, Heimes M, ..., Sinning I 10.1016/j.molcel.2020.08.012
25869254 The emerging role of calcium-modulating cyclophilin ligand in posttranslationalinsertion of tail-anchored proteins into the endoplasmic reticulum membrane Yamamoto Y, Sakisaka T 10.1093/jb/mvv035
25368153 Differential gradients of interaction affinities drive efficient targeting andrecycling in the GET pathway Rome ME, Chio US, ..., Shan SO 10.1073/pnas.1411284111
24392163 WRB and CAML are necessary and sufficient to mediate tail-anchored protein targeting to the ER membrane Vilardi F, Stephan M, ..., Schwappach B 10.1371/journal.pone.0085033
25043001 The Get1/2 transmembrane complex is an endoplasmic-reticulum membrane proteininsertase Wang F, Chan C, Weir NR, Denic V 10.1038/nature13471
26926495 Get1p and Get2p are required for maintenance of mitochondrial morphology andnormal cardiolipin levels Joshi AS, Fei N, Greenberg ML 10.1093/femsyr/fow019
29673596 The ER membrane insertase Get1/2 is required for efficient mitophagy in yeast Onishi M, Nagumo S, Iwashita S, Okamoto K 10.1016/j.bbrc.2018.04.114