About Gene List

PF3D7_1233900 (SENP1)

Genome location: Pf3D7_12_v3:1,407,068..1,411,277(+)

Genome classification: Core

Function and Localization

Product Description: sentrin-specific protease 1

SignalP Peptide: N/A

# Transmembrane Domains: 0

EC Numbers: 3.4.22.68 (Ulp1 peptidase)

Curated GO (PlasmoDB):

Type GO Term Name
Component GO:0005634 nucleus
Function GO:0016929 SUMO-specific protease activity
Process GO:0016926 protein desumoylation

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

Stage LR class MCA mean MCA prop. zeros
Sporozoite not expressed N/A N/A
Ring not expressed 0.24 0.88
Trophozoite possibly expressed 0.65 0.63
Schizont not expressed 0.35 0.78
Gametocyte not expressed 0.52 0.70

More info:

Resistome Mutations

Old (Pf3D7v3) Gene ID: PF3D7_1233900

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: 0.12 | MFS: -2.955 | #Insertions: 0

PlasmoGEM Phenotype: Essential (Pb ortholog: PBANKA_1448500)

  • Relative Growth Rate: 0.22 ± 0.42
  • Confidence: 3.12

RMgmDB ABS Phenotype: N/A

More info: PhenoPlasm Link

Binding Evidence

AlphaFill Uniprot ID: Q8I583

"Best" AlphaFill ligand hit: AYE (allylamine, Local RMSD=0.23) with 7R2E (Global RMSD=4.69)

BRENDA EC Inhibitors:

EC # Name EC Inhibitors
3.4.22.68 Ulp1 peptidase Gu-HClVEA-260hSUMO-VSN-ethylmaleimideUbiquitin aldehyde3-[(4-[[2-[(2E)-4-[bis(naphthalen-1-ylmethyl)amino]-4-oxobut-2-enoyl]-2-(carboxymethyl)hydrazinyl]carbonyl]benzyl)carbamoyl]benzoic acid3-[(4-[[2-[4-[bis(naphthalen-1-ylmethyl)amino]-2,3-dichloro-4-oxobutanoyl]-2-(carboxymethyl)hydrazinyl]carbonyl]benzyl)carbamoyl]benzoic acid3-[(4-[[2-[4-[bis(naphthalen-1-ylmethyl)amino]-3-chloro-2-hydroxy-4-oxobutanoyl]-2-(carboxymethyl)hydrazinyl]carbonyl]benzyl)carbamoyl]benzoic acid3-[(4-[[2-([(2R,3R)-3-[benzyl(cyclohexa-1,3-dien-1-ylmethyl)carbamoyl]-3-chlorooxiran-2-yl]carbonyl)-2-(carboxymethyl)hydrazinyl]carbonyl]benzyl)carbamoyl]benzoic acid

Orthology to BindingDB Entries:

UniProt Protein Name Species Homology Source BindingDB Ligands
Q96HI0 Sentrin-specific protease 5 OrthoDB CHEMBL4796113CHEMBL4780306CHEMBL4800446CHEMBL4785280...
Q9P0U3 Sentrin-specific protease 1 Homo sapiens OrthoDB VEA-260VEA-499MLS000573775MLS000058000...
Q9HC62 Sentrin-specific protease 2 Homo sapiens OrthoDB JCP-666VEA-260VEA-499VEA-500...
Q9GZR1 Sentrin-specific protease 6 Homo sapiens OrthoDB MLS000073450MLS000027210MLS000029968MLS000070601...
Q9BQF6 Sentrin-specific protease 7 Homo sapiens OrthoDB VEA-561SPI-01SPI-02NSC8676...

Orthology Information

Ortholog Group (OrthoMCL): OG6_101235

Most Similar Human Ortholog: Q9P0U3

TM-align score: 0.41 | RMSD: 4.74

Seq Identity: 0.27 | Length: 303 / 1026

All Human Orthologs (OrthoMCL):

Gene ID Description
ENSG00000079387 SUMO specific peptidase 1

Protein Information

Protein Length: 1026 | Molecular Weight (kDa): 123.225

UniProt ID(s): Q8I583

PDB ID(s): None

Isoelectric Point: 7.83

Protein Domain Annotations:

Source Family ID Description
InterPro IPR003653 Ulp1 protease family, C-terminal catalytic domain
InterPro IPR038765 Papain-like cysteine peptidase superfamily
PFam PF02902 Ulp1 protease family, C-terminal catalytic domain
Superfamily SSF54001 Papain-like cysteine peptidase superfamily

Genetic Variation

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

Homozygous genotype calls only

variant type common rare doubleton singleton
synonymous 9 51 24 64
disruptive 41 166 77 172
missense 24 119 67 142

Any inclusion in genotype call

variant type common rare doubleton singleton
synonymous 17 92 41 64
disruptive 95 311 130 328
missense 45 236 108 210

PlasmoDB Total SNPs: 252

Non-coding: 142 | Synonymous: 51 | Nonsynonymous: 59 | 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
16267556 A protein interaction network of the malaria parasite Plasmodium falciparum. LaCount DJ, Vignali M, ..., Hughes RE 10.1038/nature04104
21700207 Functional characterization of a SUMO deconjugating protease of Plasmodiumfalciparum using newly identified small molecule inhibitors. Ponder EL, Albrow VE, ..., Bogyo M 10.1016/j.chembiol.2011.04.010
23181666 Organellar proteomics reveals hundreds of novel nuclear proteins in the malariaparasite Plasmodium falciparum. Oehring SC, Woodcroft BJ, ..., Voss TS 10.1186/gb-2012-13-11-r108
37914145 SENP1 knockdown-mediated CTCF SUMOylation enhanced its stability and alleviatedlipopolysaccharide-evoked inflammatory injury in human lung fibroblasts viaregulation of FOXA2 transcription Kang L, Wang X, ..., Lei R 10.1016/j.bbagen.2023.130500