A multifunctional serine protease primes the malaria parasite for red blood cell invasion
about
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 malariaTargeting Plasmodium falciparum Hsp90: Towards Reversing Antimalarial ResistanceChemical biology approaches for the study of apicomplexan parasitesMalaria parasite cGMP-dependent protein kinase regulates blood stage merozoite secretory organelle discharge and egressThe malaria parasite egress protease SUB1 is a calcium-dependent redox switch subtilisinA novel Plasmodium-specific prodomain fold regulates the malaria drug target SUB1 subtilasePlasmodium falciparum merozoite surface protein 1 blocks the proinflammatory protein S100PProcessing of Plasmodium falciparum Merozoite Surface Protein MSP1 Activates a Spectrin-Binding Function Enabling Parasite Egress from RBCsBiophysics of malarial parasite exit from infected erythrocytesComputational reverse-engineering of a spider-venom derived peptide active against Plasmodium falciparum SUB1The malarial serine protease SUB1 plays an essential role in parasite liver stage developmentComputational design of protein-based inhibitors of Plasmodium vivax subtilisin-like 1 proteaseEctopic expression of a Neospora caninum Kazal type inhibitor triggers developmental defects in Toxoplasma and PlasmodiumSpatiotemporal and functional characterisation of the Plasmodium falciparum cGMP-dependent protein kinaseA plant-like kinase in Plasmodium falciparum regulates parasite egress from erythrocytesExpression and characterization of catalytic domain of Plasmodium falciparum subtilisin-like protease 3A DOC2 protein identified by mutational profiling is essential for apicomplexan parasite exocytosisSystematic genetic analysis of the Plasmodium falciparum MSP7-like family reveals differences in protein expression, location, and importance in asexual growth of the blood-stage parasite1H, 13C and 15N resonance assignments and secondary structure analysis of CmPI-II, a serine protease inhibitor isolated from marine snail Cenchritis muricatus.Parasitophorous vacuole poration precedes its rupture and rapid host erythrocyte cytoskeleton collapse in Plasmodium falciparum egress.The relationship between anti-merozoite antibodies and incidence of Plasmodium falciparum malaria: A systematic review and meta-analysis.Antibodies against multiple merozoite surface antigens of the human malaria parasite Plasmodium falciparum inhibit parasite maturation and red blood cell invasionIsolation and characterization of the MSP1 genes from Plasmodium malariae and Plasmodium ovaleChemical genetics.Limited variation in vaccine candidate Plasmodium falciparum Merozoite Surface Protein-6 over multiple transmission seasonsRegulated maturation of malaria merozoite surface protein-1 is essential for parasite growth.New insights for native production of MSP1(19), the disulfide-rich C-terminal fragment from Plasmodium falciparum merozoite surface protein 1.The role of serine-type serine repeat antigen in Plasmodium yoelii blood stage developmentIn Silico screening on the three-dimensional model of the Plasmodium vivax SUB1 protease leads to the validation of a novel anti-parasite compoundGlobal identification of multiple substrates for Plasmodium falciparum SUB1, an essential malarial processing protease.Exploiting unique structural and functional properties of malarial glycolytic enzymes for antimalarial drug developmentGlobal profiling of proteolysis during rupture of Plasmodium falciparum from the host erythrocyte.Small molecule targeting malaria merozoite surface protein-1 (MSP-1) prevents host invasion of divergent plasmodial species.Genetic diversity and population structure of genes encoding vaccine candidate antigens of Plasmodium vivax.Antibodies directed against merozoite surface protein-6 are induced by natural exposure to Plasmodium falciparum in a low transmission environment.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.Prison break: pathogens' strategies to egress from host cells.
P2860
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P2860
A multifunctional serine protease primes the malaria parasite for red blood cell invasion
description
2009 nî lūn-bûn
@nan
2009 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մարտին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
A multifunctional serine protease primes the malaria parasite for red blood cell invasion
@ast
A multifunctional serine protease primes the malaria parasite for red blood cell invasion
@en
type
label
A multifunctional serine protease primes the malaria parasite for red blood cell invasion
@ast
A multifunctional serine protease primes the malaria parasite for red blood cell invasion
@en
prefLabel
A multifunctional serine protease primes the malaria parasite for red blood cell invasion
@ast
A multifunctional serine protease primes the malaria parasite for red blood cell invasion
@en
P2093
P2860
P50
P921
P356
P1433
P1476
A multifunctional serine protease primes the malaria parasite for red blood cell invasion
@en
P2093
Chrislaine Withers-Martinez
Ellen Knuepfer
Fiona Hackett
Hermann Bujard
Luiz Juliano
Michael J Blackman
Sharon Yeoh
P2860
P304
P356
10.1038/EMBOJ.2009.22
P407
P577
2009-02-12T00:00:00Z