Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/19806
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dc.contributor.authorMandal, Tarun K-
dc.contributor.authorMukhopadhyay, Chaitali-
dc.date.accessioned2013-07-16T06:28:48Z-
dc.date.available2013-07-16T06:28:48Z-
dc.date.issued2001-04-
dc.identifier.issn0975-0959 (Online); 0301-1208 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/19806-
dc.description96-103en_US
dc.description.abstractIn this article we present the results of molecular modelling of four complex carbohydrates which have been found in the MHC class I proteins. Though these proteins show diversity in their sequences, the glycosylation sites are highly conserved indicating a possible structural/functional role of the glycan chain. Similar glycan chains have been found linked with other proteins of completely different function, such as IgG, and erythropoeitin. Thus, the molecular modelling of these carbohydrates will not only provide structural/dynamic information of these complex molecules but will also provide conformational information which can be utilised to build the glycoprotein model s. The results presented here indicate that although several linkages show less conformational flexibility, terminal linkages can be quite flexible.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rightsCC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJBB Vol.38(1-2) [February-April 2001]en_US
dc.titleMolecular modelling of MHC class I carbohydratesen_US
dc.typeArticleen_US
Appears in Collections:IJBB Vol.38(1-2) [February-April 2001]

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