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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2002-11-6
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pubmed:databankReference |
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pubmed:abstractText |
Trans-sialidases (TS) are GPI-anchored surface enzymes expressed in specific developmental stages of trypanosome parasites like Trypanosoma cruzi, the etiologic agent of Chagas disease, and T. brucei, the causative agent of sleeping sickness. TS catalyzes the transfer of sialic acid residues from host to parasite glycoconjugates through a transglycosidase reaction that appears to be critical for T. cruzi survival and cell invasion capability. We report here the structure of the T. cruzi trans-sialidase, alone and in complex with sugar ligands. Sialic acid binding is shown to trigger a conformational switch that modulates the affinity for the acceptor substrate and concomitantly creates the conditions for efficient transglycosylation. The structure provides a framework for the structure-based design of novel inhibitors with potential therapeutic applications.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1097-2765
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
757-68
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:12419220-Animals,
pubmed-meshheading:12419220-Binding Sites,
pubmed-meshheading:12419220-Crystallography, X-Ray,
pubmed-meshheading:12419220-Enzyme Activation,
pubmed-meshheading:12419220-Glycoproteins,
pubmed-meshheading:12419220-Lactose,
pubmed-meshheading:12419220-Models, Molecular,
pubmed-meshheading:12419220-N-Acetylneuraminic Acid,
pubmed-meshheading:12419220-Neuraminidase,
pubmed-meshheading:12419220-Protein Conformation,
pubmed-meshheading:12419220-Static Electricity,
pubmed-meshheading:12419220-Structure-Activity Relationship,
pubmed-meshheading:12419220-Substrate Specificity,
pubmed-meshheading:12419220-Trypanosoma cruzi
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pubmed:year |
2002
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pubmed:articleTitle |
The crystal structure and mode of action of trans-sialidase, a key enzyme in Trypanosoma cruzi pathogenesis.
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pubmed:affiliation |
Unité de Biochimie Structurale, CNRS URA 2185, Institut Pasteur, 25 rue du Dr. Roux, 75724, Paris, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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