Genome location: Pf3D7_13_v3:2,786,609..2,789,345(+)
Genome classification: Core
Product Description: membrane associated histidine-rich protein 1
SignalP Peptide: N/A
# Transmembrane Domains: 1
EC Numbers: None
Curated GO (PlasmoDB):
Type | GO Term | Name |
---|---|---|
Component | GO:0020036 | Maurer's cleft |
Component | GO:1903561 | extracellular vesicle |
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 | no data | N/A | N/A |
Ring | no data | 2.15 | 0.30 |
Trophozoite | no data | 0.53 | 0.77 |
Schizont | no data | 0.35 | 0.82 |
Gametocyte | no data | 0.35 | 0.82 |
More info:
Old (Pf3D7v3) Gene ID: PF3D7_1370300
Resistome Missense Mutations: None
Resistome Compounds with Missense Mutations: None
Resistome # Samples with Disruptive Mutations: 0 (0 missense, 0 "interesting" missense)
Zhang Phenotype: Non - Mutable in CDS *tentative
MIS: 0.964 | MFS: -2.237 | #Insertions: 0
PlasmoGEM Phenotype: N/A
RMgmDB ABS Phenotype: Different from wild type (Pb ortholog: PBANKA_1145900)
Modification: Disrupted | RMgm-3165
More info: PhenoPlasm Link
AlphaFill Uniprot ID: C0H5L9
"Best" AlphaFill ligand hit: No AlphaFill hits
No associated EC numbersNo evidence of orthology to BindingDB entries
MalariaGEN Pf7 (worldwide samples) # unique SNV/indels:
Homozygous genotype calls only
variant type | common | rare | doubleton | singleton |
---|---|---|---|---|
synonymous | 2 | 13 | 3 | 15 |
disruptive | 25 | 19 | 6 | 41 |
missense | 13 | 4 | 3 | 18 |
Any inclusion in genotype call
variant type | common | rare | doubleton | singleton |
---|---|---|---|---|
synonymous | 9 | 12 | 11 | 14 |
disruptive | 33 | 44 | 27 | 73 |
missense | 14 | 13 | 14 | 46 |
PlasmoDB Total SNPs: 87
Non-coding: 49 | Synonymous: 21 | Nonsynonymous: 17 | Stop Codon: 0
PMID | Title | Authors | DOI/Link |
---|---|---|---|
12815049 | MAHRP-1, a novel Plasmodium falciparum histidine-rich protein, bindsferriprotoporphyrin IX and localizes to the Maurer's clefts. | Spycher C, Klonis N, ..., Beck HP | 10.1074/jbc.M305851200 |
28944300 | Proteomic analysis of extracellular vesicles from a Plasmodium falciparum Kenyanclinical isolate defines a core parasite secretome. | Abdi A, Yu L, ..., Rayner J | 10.12688/wellcomeopenres.11910.2 |
31476617 | A High-Resolution Map of SBP1 Interactomes in Plasmodium falciparum-infectedErythrocytes. | Takano R, Kozuka-Hata H, ..., Kato K | 10.1016/j.isci.2019.07.035 |
32184257 | Role of Plasmodium falciparum Protein G EXP07 in Maurer's Cleft Morphology, Knob Architecture, and P. falciparum E MP1 Trafficking | McHugh E, Carmo OMS, ..., Dixon MWA | 10.1128/mBio.03320-19 |
27225796 | The machinery underlying malaria parasite virulence is conserved between rodentand human malaria parasites | De Niz M, Ullrich AK, ..., Spielmann T | 10.1038/ncomms11659 |
16705161 | Genesis of and trafficking to the Maurer's clefts of Plasmodiumfalciparum-infected erythrocytes | Spycher C, Rug M, ..., Tilley L | 10.1128/MCB.00095-06 |
18410498 | The Maurer's cleft protein MAHRP1 is essential for trafficking of PfEMP1 to thesurface of Plasmodium falciparum-infected erythrocytes | Spycher C, Rug M, ..., Beck HP | 10.1111/j.1365-2958.2008.06235.x |
19166814 | A Maurer's cleft-associated Plasmodium falciparum membrane-associatedhistidine-rich protein peptide specifically interacts with the erythrocytemembrane | Garcia J, Curtidor H, ..., Patarroyo ME | 10.1016/j.bbrc.2009.01.050 |