GPI-anchored proteins and free GPI glycolipids of procyclic form Trypanosoma brucei are nonessential for growth, are required for colonization of the tsetse fly, and are not the only components of the surface coat.

GPI-anchored proteins and free GPI glycolipids of procyclic form Trypanosoma brucei are nonessential for growth, are required for colonization of the tsetse fly, and are not the only components of the surface coat.

Item

http://www.wikidata.org/entity/Q35191010

Q35191010

about

Mammalian African trypanosome VSG coat enhances tsetse's vector competence De novo sphingolipid synthesis is essential for viability, but not for transport of glycosylphosphatidylinositol-anchored proteins, in African trypanosomes.PSSA-2, a membrane-spanning phosphoprotein of Trypanosoma brucei, is required for efficient maturation of infection Deletion of the TbALG3 gene demonstrates site-specific N-glycosylation and N-glycan processing in Trypanosoma brucei.Major surface glycoproteins of insect forms of Trypanosoma brucei are not essential for cyclical transmission by tsetse High-confidence glycosome proteome for procyclic form Trypanosoma brucei by epitope-tag organelle enrichment and SILAC proteomics.Sphingolipids in parasitic protozoa KREX2 is not essential for either procyclic or bloodstream form Trypanosoma brucei.Modeling of the N-glycosylated transferrin receptor suggests how transferrin binding can occur within the surface coat of Trypanosoma brucei.Effects of ingested vertebrate-derived factors on insect immune responses.Identification and functional analysis of Trypanosoma cruzi genes that encode proteins of the glycosylphosphatidylinositol biosynthetic pathway.Redirection of sphingolipid metabolism toward de novo synthesis of ethanolamine in Leishmania.myo-Inositol uptake is essential for bulk inositol phospholipid but not glycosylphosphatidylinositol synthesis in Trypanosoma brucei.Flagellar membranes are rich in raft-forming phospholipids Inositolphosphoceramide metabolism in Trypanosoma cruzi as compared with other trypanosomatids.The effects of ingested mammalian blood factors on vector arthropod immunity and physiology The synthesis of UDP-N-acetylglucosamine is essential for bloodstream form trypanosoma brucei in vitro and in vivo and UDP-N-acetylglucosamine starvation reveals a hierarchy in parasite protein glycosylation.Developmentally regulated sphingolipid synthesis in African trypanosomes Differential trypanosome surface coat regulation by a CCCH protein that co-associates with procyclin mRNA cis-elements.Lipidomic analysis of bloodstream and procyclic form Trypanosoma brucei Fate of glycosylphosphatidylinositol (GPI)-less procyclin and characterization of sialylated non-GPI-anchored surface coat molecules of procyclic-form Trypanosoma brucei.Molecular docking and molecular dynamics simulation study of inositol phosphorylceramide synthase - inhibitor complex in leishmaniasis: Insight into the structure based drug design.Tsetse flies, trypanosomes, humans and animals: what is proteomics revealing about their crosstalks?Trypanosoma brucei: a model micro-organism to study eukaryotic phospholipid biosynthesis.Leishmania (Viannia) braziliensis Inositol Phosphorylceramide: Distinctive Sphingoid Base Composition.TbGT8 is a bifunctional glycosyltransferase that elaborates N-linked glycans on a protein phosphatase AcP115 and a GPI-anchor modifying glycan in Trypanosoma brucei.Identification of a glycosylphosphatidylinositol anchor-modifying β1-3 galactosyltransferase in Trypanosoma brucei Characterization of inositol phosphorylceramides from Leishmania major by tandem mass spectrometry with electrospray ionization.The Glycerol-3-Phosphate Acyltransferase TbGAT is Dispensable for Viability and the Synthesis of Glycerolipids in Trypanosoma brucei.Lipidomics and anti-trypanosomatid chemotherapy.The Sphingolipid Biosynthetic Pathway Is a Potential Target for Chemotherapy against Chagas Disease.The essential neutral sphingomyelinase is involved in the trafficking of the variant surface glycoprotein in the bloodstream form of Trypanosoma brucei.Single-subunit oligosaccharyltransferases of Trypanosoma brucei display different and predictable peptide acceptor specificities.UDP-glycosyltransferase genes in trypanosomatid genomes have diversified independently to meet the distinct developmental needs of parasite adaptations.The mRNA cap methyltransferase gene TbCMT1 is not essential in vitro but is a virulence factor in vivo for bloodstream form Trypanosoma brucei

P2860

Q26314596-0E6FC6F6-08BE-4E93-818C-D3271049CE3C Q30444720-C069F29C-AD34-4134-B0F1-3CB436B834BF Q30873805-B8CF75C0-623C-4F7A-AABD-E706CEA78384 Q33319071-BC6C6207-CF15-4ABB-8401-4849AC026525 Q33410086-348E9042-3E8A-4947-9A71-0BC68B297A0B Q33738172-0C013D09-2731-4174-B4A5-0AD1C68E6EEA Q34183686-07EBA0C9-2089-46B7-ADD1-D59AB59233B0 Q34206225-EA28EC1F-AEEC-48CB-AEF5-D239933BF60D Q34229614-2661738E-69FC-47B7-B288-3BA272EF7D43 Q34495755-2563AA69-FC82-47EC-9BCA-6464BAD8B9A9 Q34952443-B8F8E957-6DD5-48BF-85BE-5946A9958941 Q35752867-81FC3468-CCC7-48D0-91EA-8B2B64834315 Q35921715-E93D5211-C762-4D66-93C3-1CC52CE852F7 Q36090878-0694E79E-99BF-4565-BCD9-EC029DEC8B21 Q36240220-84DEB8B4-DF24-4203-93EF-ABB09C0095EB Q36698998-D401B487-89C9-49C9-80EC-8ABCA6E80BB2 Q36701780-902B7810-46F6-497A-93F1-246F689E09BC Q37069574-FA04A92A-DDEF-4D14-B156-0D4924C5A06F Q37097303-87781D7D-5409-4A7E-A814-DCB65831048F Q37098724-60210D40-7DDE-450B-B181-614AEA24A616 Q37355723-B02D6540-2ABA-49E4-94CD-28D0E9047E86 Q37384258-BEF0AD9A-DE11-4E74-A6B4-A64540913CDD Q37685121-FF7D08C9-7BD4-44D8-909D-F19E1D25419B Q37828174-B4649D8D-0AF2-45D4-ABCB-9EE4B293A4BC Q38639793-E382192F-30AA-4A06-8E3F-42D26AE74C93 Q39031763-1C55BD63-242A-4DD1-A8C0-F0C464157137 Q39097406-9558DA36-A51B-4BD4-B59E-9695DED3AC4A Q39776750-DE808713-5378-498D-A1D1-C82B3CDB15F6 Q39973082-B19CE963-7186-45AF-9A42-1A2BACAC4B82 Q41203049-EA790BC4-9A86-485F-AC1A-8B876F1C9519 Q42731998-BC922699-B78F-4792-A906-3F843EA71E26 Q42732779-8BE9B6FE-E1EC-40FD-B236-269F1857B242 Q45945583-39A9FCA5-D97A-4DB5-811D-73354944B637 Q52655663-478B3E32-E944-45A5-A89E-D412C724B797 Q58867158-DEC87DF8-15BA-4AF4-927E-17381EEA1396

P2860

GPI-anchored proteins and free GPI glycolipids of procyclic form Trypanosoma brucei are nonessential for growth, are required for colonization of the tsetse fly, and are not the only components of the surface coat.

Item

http://www.wikidata.org/entity/Q35191010

description

2006 nî lūn-bûn

@nan

2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2006年の論文

@ja

2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

@wuu