About Gene List

PF3D7_1474800

Genome location: Pf3D7_14_v3:3,066,856..3,069,024(+)

Genome classification: Core

Function and Localization

Product Description: proteasome subunit alpha type-1, putative

SignalP Peptide: N/A

# Transmembrane Domains: 0

EC Numbers: 3.4.25.1 (Proteasome endopeptidase complex)

Curated GO (PlasmoDB):

Type GO Term Name
Component GO:0005737 cytoplasm
Component GO:0005634 nucleus
Component GO:0005839 proteasome core complex
Component GO:0019773 proteasome core complex, alpha-subunit complex
Function GO:0004175 endopeptidase activity
Process GO:0010498 proteasomal protein catabolic process
Process GO:0010499 proteasomal ubiquitin-independent protein catabolic process
Process GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process
Process GO:0006511 ubiquitin-dependent protein catabolic process

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 0.06 0.97
Trophozoite expressed 0.30 0.81
Schizont expressed 0.08 0.94
Gametocyte expressed 0.17 0.90

More info:

Resistome Mutations

Old (Pf3D7v3) Gene ID: PF3D7_1474800

Resistome Missense Mutations: None

Resistome Compounds with Missense Mutations: None

Resistome # Samples with Disruptive Mutations: 0 (0 missense, 0 "interesting" missense)

Essentiality (ABS)

Zhang Phenotype: Non - Mutable in CDS

MIS: 0.196 | MFS: -2.545 | #Insertions: 0

PlasmoGEM Phenotype: Essential (Pb ortholog: PBANKA_1301400)

  • Relative Growth Rate: 0.10 ± nan
  • Confidence: 1.00

RMgmDB ABS Phenotype: N/A

More info: PhenoPlasm Link

Binding Evidence

AlphaFill Uniprot ID: Q8IK90

"Best" AlphaFill ligand hit: No AlphaFill hits

BRENDA EC Inhibitors:

EC # Name EC Inhibitors
3.4.25.1 proteasome endopeptidase complex ATPSDSPSIEDTANH4+EGTATLCKALLNNMDANLVSPI 1PA28...

Orthology to BindingDB Entries:

UniProt Protein Name Species Homology Source BindingDB Ligands
P25786 Proteasome subunit alpha type-1 HOGENOM, OrthoDB CHEMBL4872258CHEMBL4877708
P23639 Proteasome subunit alpha type-2 OrthoDB Carmaphycin A (1)(2S)-N-[(4S)-2,6-dimethyl-3-oxohept-1-en-4-yl]-2-[(2S)-2-hexanamido-3-methylbutanamido]-N',N'-dimethylpentanediamide (4)(2S)-N-[(4S)-2,6-dimethyl-3-oxohept-1-en-4-yl]-2-[(2S)-2-hexanamido-3-methylbutanamido]-N',N'-dimethylpentanediamide (4)Carmaphycin A (1)...
P60900 Proteasome subunit alpha type-6 OrthoDB cid_66069med.21724, Compound 15CPZ analog, 2CPZ analog, 5...

Orthology Information

Ortholog Group (OrthoMCL): OG6_102143

Most Similar Human Ortholog: P25786

TM-align score: 0.92 | RMSD: 1.51

Seq Identity: 0.40 | Length: 243 / 254

All Human Orthologs (OrthoMCL):

Gene ID Description
ENSG00000129084 proteasome 20S subunit alpha 1

Protein Information

Protein Length: 254 | Molecular Weight (kDa): 28.838

UniProt ID(s): Q8IK90

PDB ID(s): 5FMG

Isoelectric Point: 5.42

Protein Domain Annotations:

Source Family ID Description
InterPro IPR000426 Proteasome alpha-subunit, N-terminal domain
InterPro IPR001353 Proteasome, subunit alpha/beta
InterPro IPR029055 Nucleophile aminohydrolases, N-terminal
InterPro IPR035144 Proteasome subunit alpha 1
PFam PF00227 Proteasome, subunit alpha/beta
PFam PF10584 Proteasome alpha-subunit, N-terminal domain
Superfamily SSF56235 Nucleophile aminohydrolases, N-terminal

Genetic Variation

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

Homozygous genotype calls only

variant type common rare doubleton singleton
synonymous 1 27 7 12
disruptive 5 13 6 25
missense 3 13 6 25

Any inclusion in genotype call

variant type common rare doubleton singleton
synonymous 5 39 10 11
disruptive 7 31 25 65
missense 5 28 21 50

PlasmoDB Total SNPs: 161

Non-coding: 150 | Synonymous: 6 | Nonsynonymous: 5 | Stop Codon: 0

Associated Publications

PMID Title Authors DOI/Link
12368864 Genome sequence of the human malaria parasite Plasmodium falciparum. Gardner MJ, Hall N, ..., Barrell B 10.1038/nature01097
30379851 Identification of Plasmodium falciparum nuclear proteins by mass spectrometry andproposed protein annotation. Briquet S, Ourimi A, ..., Vaquero C 10.1371/journal.pone.0205596