Global identification of multiple substrates for Plasmodium falciparum SUB1, an essential malarial processing protease.
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The cellular and molecular basis for malaria parasite invasion of the human red blood cellMerozoite surface proteins in red blood cell invasion, immunity and vaccines against malariaRecent insights into apicomplexan parasite egress provide new views to a killMalaria parasite cGMP-dependent protein kinase regulates blood stage merozoite secretory organelle discharge and egressInsights into Duffy Binding-like Domains through the Crystal Structure and Function of the Merozoite Surface Protein MSPDBL2 from Plasmodium falciparumMicroneme Protein 5 Regulates the Activity of Toxoplasma Subtilisin 1 by Mimicking a Subtilisin ProdomainA novel Plasmodium-specific prodomain fold regulates the malaria drug target SUB1 subtilaseProcessing of Plasmodium falciparum Merozoite Surface Protein MSP1 Activates a Spectrin-Binding Function Enabling Parasite Egress from RBCsThe merozoite surface protein 1 complex is a platform for binding to human erythrocytes by Plasmodium falciparumCalcium-dependent permeabilization of erythrocytes by a perforin-like protein during egress of malaria parasitesHost cell remodeling by pathogens: the exomembrane system in Plasmodium-infected erythrocytesThe malarial serine protease SUB1 plays an essential role in parasite liver stage developmentComputational design of protein-based inhibitors of Plasmodium vivax subtilisin-like 1 proteaseP113 is a merozoite surface protein that binds the N terminus of Plasmodium falciparum RH5Expression and characterization of catalytic domain of Plasmodium falciparum subtilisin-like protease 3The Apicomplexan CDC/MACPF-like pore-forming proteins.Parasitophorous vacuole poration precedes its rupture and rapid host erythrocyte cytoskeleton collapse in Plasmodium falciparum egress.Juxtamembrane shedding of Plasmodium falciparum AMA1 is sequence independent and essential, and helps evade invasion-inhibitory antibodiesProtease-associated cellular networks in malaria parasite Plasmodium falciparum.The Plasmodium vivax rhoptry neck protein 5 is expressed in the apical pole of Plasmodium vivax VCG-1 strain schizonts and binds to human reticulocytes.Proteases in malaria parasites - a phylogenomic perspective.Molecular dissection of novel trafficking and processing of the Toxoplasma gondii rhoptry metalloprotease toxolysin-1.Plasmodium subtilisin-like protease 1 (SUB1): insights into the active-site structure, specificity and function of a pan-malaria drug target.The role of cGMP signalling in regulating life cycle progression of Plasmodium.Proteolytic activation of the essential parasitophorous vacuole cysteine protease SERA6 accompanies malaria parasite egress from its host erythrocyte.Recent advances in recombinant protein-based malaria vaccines.Molecular determinants of binding to the Plasmodium subtilisin-like protease 1.In silico study of subtilisin-like protease 1 (SUB1) from different Plasmodium species in complex with peptidyl-difluorostatones and characterization of potent pan-SUB1 inhibitorsSerine Proteases of Malaria Parasite Plasmodium falciparum: Potential as Antimalarial Drug Targets.Proteases as regulators of pathogenesis: examples from the Apicomplexa.Human erythrocyte remodelling during Plasmodium falciparum malaria parasite growth and egress.Proteases as antimalarial targets: strategies for genetic, chemical, and therapeutic validation.A protease cascade regulates release of the human malaria parasite Plasmodium falciparum from host red blood cells.Plasmepsins on the antimalarial hit list.The cysteine protease dipeptidyl aminopeptidase 3 does not contribute to egress of Plasmodium falciparum from host red blood cellsPlasmodium falciparum dipeptidyl aminopeptidase 3 activity is important for efficient erythrocyte invasion by the malaria parasite.Polymorphism in merozoite surface protein-7E of Plasmodium vivax in Thailand: Natural selection related to protein secondary structure.The Actinomyosin Motor Drives Malaria Parasite Red Blood Cell Invasion but Not Egress.Tackling resistance: emerging antimalarials and new parasite targets in the era of eliminationFunctional Characterization of Plasmodium falciparum Surface-Related Antigen as a Potential Blood-Stage Vaccine Target
P2860
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P2860
Global identification of multiple substrates for Plasmodium falciparum SUB1, an essential malarial processing protease.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Global identification of multi ...... malarial processing protease.
@ast
Global identification of multi ...... malarial processing protease.
@en
Global identification of multi ...... malarial processing protease.
@nl
type
label
Global identification of multi ...... malarial processing protease.
@ast
Global identification of multi ...... malarial processing protease.
@en
Global identification of multi ...... malarial processing protease.
@nl
prefLabel
Global identification of multi ...... malarial processing protease.
@ast
Global identification of multi ...... malarial processing protease.
@en
Global identification of multi ...... malarial processing protease.
@nl
P2093
P2860
P50
P356
P1476
Global identification of multi ...... malarial processing protease.
@en
P2093
Chrislaine Withers-Martinez
Fiona Hackett
J Mark Skehel
Marta G Campos
Michael J Blackman
P2860
P304
P356
10.1128/IAI.00902-10
P407
P577
2011-01-10T00:00:00Z