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Plasmepsin
Membrane Proteins • Cofactors – Plimstex • Membranes • Dna • Small Molecules/Gas • Large Complexes
Serine Proteases with Altered Sensitivity to Activity-Modulating
Protease Inhibition—An Established Strategy to Combat Infectious Diseases
Data-Mining Approaches Reveal Hidden Families of Proteases in The
Understanding the Structural Basis of Substrate Recognition By
Nepenthesin from Monkey Cups for Hydrogen/Deuterium Exchange Mass Spectrometry
Handbook of Proteolytic Enzymes Second Edition Volume 1 Aspartic and Metallo Peptidases
1 Peptide Therapeutics
Overexpression of Plasmepsin II and Plasmepsin III Does Not Directly Cause Reduction in Plasmodium Falciparum Sensitivity to Artesunate, Chloroquine T and Piperaquine
A Target Safety Assessment of the Potential Toxicological Risks Of
Hemoglobin-Degrading, Aspartic Proteases of Blood-Feeding Parasites SUBSTRATE SPECIFICITY REVEALED by HOMOLOGY MODELS*
Interactions of Ganoderiol-F with Aspartic Proteases of Hiv and Plasmepsin for Anti-Hiv and Anti-Malaria Discovery
Catestatin, an Endogenous Chromogranin A-Derived Peptide, Inhibits in Vitro Growth of Plasmodium Falciparum
(12) United States Patent (10) Patent No.: US 8,561,811 B2 Bluchel Et Al
Downloaded 10/1/2021 8:14:38 AM
Wo 2010/021872 A2
High Level Expression and Characterisation of Plasmepsin II, an Aspartic Proteinase from Plasmodium Falciparum
Part One Overview of Aspartic Acid Proteases
Top View
Antimalarial Activity of Human Immunodeficiency Virus Type 1 Protease Inhibitors Sunil Parikh University of California - San Francisco
Ligand Binding Site Superposition and Comparison Based on Atomic
(12) United States Patent (10) Patent No.: US 8,455,218 B2
Supplementary Material (ESI) for Natural Product Reports
Cathepsin D Deficiency Is Associated with a Human Neurodegenerative
Springer Handbook of Enzymes
Computational Study of Plasmodium Falciparum Plasmepsin II Inhibitor Binding
Protease Inhibitors: Emphasizing Functional Aspects of Aspartic Protease Inhibitors Vishnu Menon • Mala Rao*
Investigating Alternative Acidic Proteases for H/D Exchange Coupled to Mass Spectrometry: Plasmepsin 2 but Not Plasmepsin 4 Is Active Under Quenching Conditions
Plasmepsin Inhibitors: A
A Unique Structural and Dynamic Feature of Aspartic Protease
Computational Study of Triterpenoids of Ganoderma Lucidum with Aspartic Protease Enzymes for Discovering HIV-1 and Plasmepsin Inhibitors
Structural Investigation and In-Silico Characterization of Plasmepsins from Plasmodium Falciparum Divya N
Structural Aspects of Activation Pathways of Aspartic Protease Zymogens and Viral 3C Protease Precursors
Antimalarial Effects of Human Immunodeficiency Virus Type 1
WO 2016/197190 Al 15 December 2016 (15.12.2016) P O P C T
Crystal Structures of the Histo-Aspartic Protease (HAP) from Plasmodium Falciparum
MOLLUSC Nerita Versicolor
University of London Thesis
Types and Categorization of Protease Inhibitors And
Structure and Inhibition of Plasmepsin II, a Hemoglobin-Degrading Enzyme
Protein Science ~1999!, 8:2001–2009
A Distinct Member of the Aspartic Proteinase Gene Family from the Human Malaria Parasite Plasmodium Falciparum
Crystal Structures of the Free and Inhibited Forms of Plasmepsin I (PMI) from Plasmodium Falciparum
Essentiality of Plasmodium Falciparum Plasmepsin V
UQ80638 OA.Pdf
The Zymogen of Plasmepsin V from Plasmodium Falciparum Is
An Aspartyl Protease Defines a Novel Pathway for Export of Toxoplasma Proteins
Inhibition of Plasmepsin V Activity Demonstrates Its Essential Role in Protein Export, Pfemp1 Display, and Survival of Malaria Parasites
Computational Methods in Drug Discovery
(12) United States Patent (10) Patent No.: US 9,102,756 B2 Bachovchin Et Al
Function and Essentiality of Plasmodium Falciparum Plasmepsin V
Computational Analysis of Functional Sites in Proteins