You can find more information about
histo-aspartic protease
using the following links:
PFID
PFID Old
Formal Annotation
PlasmoDB
TDR Targets
Subcellular Localization
Affecting Drugs
Drug Name
PubMed Articles (year of publication)
PF3D7_1408100
PF14_0078
plasmepsin III histo-aspartic protease
PlasmoDB
TDR
(4R)-N-tert-Butyl-3-[(2S,3S)-2-hydroxy-3-({N-[(isoquinolin-5-yloxy)acetyl]-S-methyl-L-cysteinyl}amino)-4-phenylbutanoyl]-1,3-thiazolidine-4-carboxamide
High-affinity inhibition of a family of Plasmodium falciparum proteases by a designed adaptive inhibitor
4-(5-(4-methoxyphenyl)- 1’phenyl-3’-(p-tolyl)-3,4- 1’H,2H-[3,4’-bipyrazol]-2- yl)benezenesulfonamide
Molecular docking and dynamics studies on novel benzene sulfonamide substituted pyrazole-pyrazoline analogues as potent inhibitors of Plasmodium falciparum Histo aspartic protease
Alln
Role of Plasmodium falciparum digestive vacuole plasmepsins in the specificity and antimalarial mode of action of cysteine and aspartic protease inhibitors
Atazanavir
Critical roles for the digestive vacuole plasmepsins of Plasmodium falciparum in vacuolar function
Diphenylurea
Role of Plasmodium falciparum digestive vacuole plasmepsins in the specificity and antimalarial mode of action of cysteine and aspartic protease inhibitors
Doxorubicin
Discovery of plasmepsin inhibitors by fragment-based docking and consensus scoring
E-64
Critical roles for the digestive vacuole plasmepsins of Plasmodium falciparum in vacuolar function
Role of Plasmodium falciparum digestive vacuole plasmepsins in the specificity and antimalarial mode of action of cysteine and aspartic protease inhibitors
Fragment-based docking and consensus scoring, halofantrine, doxorubicin, lumefantrine
Discovery of plasmepsin inhibitors by fragment-based docking and consensus scoring
G16
Functional profiling, identification, and inhibition of plasmepsins in intraerythrocytic malaria parasites
Halofantrine
Discovery of plasmepsin inhibitors by fragment-based docking and consensus scoring
Indinavir
Critical roles for the digestive vacuole plasmepsins of Plasmodium falciparum in vacuolar function
Kni-10006
Crystal structures of the histo-aspartic protease (HAP) from Plasmodium falciparum
Kni-10395
Structural insights into the activation and inhibition of histo-aspartic protease from Plasmodium falciparum
Leupeptin
Critical roles for the digestive vacuole plasmepsins of Plasmodium falciparum in vacuolar function
Role of Plasmodium falciparum digestive vacuole plasmepsins in the specificity and antimalarial mode of action of cysteine and aspartic protease inhibitors
Lopinavir
Critical roles for the digestive vacuole plasmepsins of Plasmodium falciparum in vacuolar function
Lumefantrine
Discovery of plasmepsin inhibitors by fragment-based docking and consensus scoring
Nelfinavir
Critical roles for the digestive vacuole plasmepsins of Plasmodium falciparum in vacuolar function
Pepstatin a
Crystal structures of the histo-aspartic protease (HAP) from Plasmodium falciparum
Antimalarial activity of thiosemicarbazones and purine derived nitriles
Role of Plasmodium falciparum digestive vacuole plasmepsins in the specificity and antimalarial mode of action of cysteine and aspartic protease inhibitors
Molecular modeling and prediction of binding mode and relative binding affinity of Art-Qui-OH with P. falciparum Histo-Aspartic Protease (HAP)
Purine
Antimalarial activity of thiosemicarbazones and purine derived nitriles
Ritonavir
Critical roles for the digestive vacuole plasmepsins of Plasmodium falciparum in vacuolar function
Ro 40-4388
Role of Plasmodium falciparum digestive vacuole plasmepsins in the specificity and antimalarial mode of action of cysteine and aspartic protease inhibitors
Saquinavir
Critical roles for the digestive vacuole plasmepsins of Plasmodium falciparum in vacuolar function
Sucralfate
A systematic in silico search for target similarity identifies several approved drugs with potential activity against the Plasmodium falciparum apicoplast
Suggested target
Genetic disruption of the Plasmodium falciparum digestive vacuole plasmepsins demonstrates their functional redundancy
X-ray structures and 3d models , suggested target
Predicting functional residues in Plasmodium falciparum plasmepsins by combining sequence and structural analysis with molecular dynamics simulations
ZINC02619047
Unveiling a New Era in Malaria Therapeutics: A Tailored Molecular Approach Towards the Design of Plasmepsin IX Inhibitors
Expasy - NiceZime View
Brenda - The Comprehensive Enzyme Information System