About Gene List

PF3D7_1472200 (HDA1)

Genome location: Pf3D7_14_v3:2,944,069..2,953,562(+)

Genome classification: Core

Function and Localization

Product Description: histone deacetylase, putative

SignalP Peptide: N/A

# Transmembrane Domains: 3

EC Numbers: 3.5.1.98 (Histone deacetylase)

Curated GO (PlasmoDB):

Type GO Term Name
Component GO:0005634 nucleus

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

Stage LR class MCA mean MCA prop. zeros
Sporozoite expressed N/A N/A
Ring expressed 1.79 0.34
Trophozoite expressed 1.19 0.43
Schizont expressed 0.94 0.51
Gametocyte expressed 1.50 0.34

More info:

Resistome Mutations

Old (Pf3D7v3) Gene ID: PF3D7_1472200

Resistome Missense Mutations: L667M, N673K, N677K, N679K, N682K, N684K, E2084G

Resistome Compounds with Missense Mutations: AN13762, AN13956, MMV665794

Resistome # Samples with Disruptive Mutations: 8 (8 missense, 0 "interesting" missense)

Essentiality (ABS)

Zhang Phenotype: Non - Mutable in CDS

MIS: 0.151 | MFS: -2.835 | #Insertions: 0

PlasmoGEM Phenotype: N/A

RMgmDB ABS Phenotype: N/A

More info: PhenoPlasm Link

Binding Evidence

AlphaFill Uniprot ID: A0A144A4T0

"Best" AlphaFill ligand hit: TSN (trichostatin a, Local RMSD=0.04) with 1T64 (Global RMSD=5.51)

BRENDA EC Inhibitors:

EC # Name EC Inhibitors
3.5.1.98 histone deacetylase EDTAPAOASAHAFOXPFK228MCP30shRNAsiRNAMS-275LAQ824MC1575MC1568...

No evidence of orthology to BindingDB entries

Orthology Information

Ortholog Group (OrthoMCL): OG6_114105

No human ortholog(s)

Genetic Variation

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

Homozygous genotype calls only

variant type common rare doubleton singleton
synonymous 31 127 82 147
disruptive 96 305 141 342
missense 53 233 119 261

Any inclusion in genotype call

variant type common rare doubleton singleton
synonymous 48 254 111 159
disruptive 180 583 279 608
missense 98 425 206 364

PlasmoDB Total SNPs: 491

Non-coding: 199 | Synonymous: 193 | Nonsynonymous: 99 | Stop Codon: 0

Protein Information

Protein Length: 2251 | Molecular Weight (kDa): 268.92

UniProt ID(s): A0A144A4T0

PDB ID(s): None

Isoelectric Point: 9.35

Protein Domain Annotations:

Source Family ID Description
InterPro IPR000286 Histone deacetylase family
InterPro IPR023696 Ureohydrolase domain superfamily
InterPro IPR023801 Histone deacetylase domain
InterPro IPR036770 Ankyrin repeat-containing domain superfamily
PFam PF00850 Histone deacetylase domain
Superfamily SSF48403 Ankyrin repeat-containing domain superfamily
Superfamily SSF52768 Ureohydrolase domain superfamily

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
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
36993207 The chromatin factors SET-26 and HCF-1 oppose the histone deacetylase HDA-1 inlongevity and gene regulation in C. elegans Emerson FJ, Chiu C, ..., Lee SS 10.1101/2023.03.20.531974
38334386 The histone deacetylase Hda1 affects oxidative and osmotic stress response aswell as mycoparasitic activity and secondary metabolite biosynthesis in Trichoderma atroviride Speckbacher V, Flatschacher D, ..., Zeilinger S 10.1128/spectrum.03097-23
37874684 The Saccharomyces cerevisiae acetyltransferase Gcn5 exerts antagonisticpleiotropic effects on chronological ageing Li K, Mocciaro G, Griffin JL, Zhang N 10.18632/aging.205109
37074817 Origin of the kinetic HDAC2-selectivity of an HDAC inhibitor Mishima H, Itoh Y, ..., Okamoto Y 10.1002/jcc.27111