You can find more information about proteasome subunit beta type-5 using the following links:

PFID

PFID Old

Formal Annotation

PlasmoDB

TDR Targets

Subcellular Localization

Affecting Drugs

Drug Name

PubMed Articles (year of publication)

PF3D7_1011400

PF10_0111

proteasome subunit beta type-5

((R)-1-((S)-2-(2-(4-hydroxyphenyl)acetamido)-3-phenylpropanamido)-3-methylbutyl)boronic acid	Target Validation and Identification of Novel Boronate Inhibitors of the Plasmodium falciparum Proteasome
(2S)-3-methyl-2-[[(2S)-2-[[(2S)-2-[methyl(pyrazin-2-yl)amino]-4-phenyl-butanoyl]amino]-4-phenyl-butanoyl]amino]-N-(m-tolylmethyl)butanamide	Identification of potent and selective non-covalent inhibitors of the Plasmodium falciparum proteasome
(S)-N4-(tert-butyl)-N1-(2-(2',4-difluoro-[1,1'-biphenyl]-3-carboxamido)ethyl)-2-((4-methylphenyl)sulfonamido)succinamide	Antimalarial proteasome inhibitor reveals collateral sensitivity from intersubunit interactions and fitness cost of resistance
(S)-N4-(tert-butyl)-N1-(2-(3-ethynylbenzamido)ethyl)-2-((4-methylphenyl)sulfonamido)succinamide	Improvement of Asparagine Ethylenediamines as Anti-malarial Plasmodium-Selective Proteasome Inhibitors
Benzo[b]thiophene	Identification of potent and selective non-covalent inhibitors of the Plasmodium falciparum proteasome
Bortezomib	Analysis of bortezomib inhibitor docked within the catalytic subunits of the Plasmodium falciparum 20S proteasome
Epoxomicin	Plasmodia express two threonine-peptidase complexes during asexual development The proteasome inhibitor epoxomicin has potent Plasmodium falciparum gametocytocidal activity
Epoxyketone	Assessing subunit dependency of the Plasmodium proteasome using small molecule inhibitors and active site probes
N-[(2S)-3-Methyl-1-{[(2S)-1-({(2S)-4-methyl-1-[(2R)-2-methyl-2-oxiranyl]-1-oxo-2-pentanyl}amino)-4-(methylsulfonyl)-1-oxo-2-butanyl]amino}-1-oxo-2-butanyl]hexanamide	Development of a Potent Inhibitor of the Plasmodium Proteasome with Reduced Mammalian Toxicity
N-[3-methyl-1-[[1-[[4-methyl-1-[(2R)-2-methyloxiran-2-yl]-1-oxo-pentyl]amino]-1-oxo-pentyl]amino]-1-oxo-butyl]hexanamide	Development of a Potent Inhibitor of the Plasmodium Proteasome with Reduced Mammalian Toxicity

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