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dc.contributor.authorBiswas, Sumit
dc.contributor.authorGuharoy, Mainak
dc.contributor.authorChakrabarti, Pinakpani
dc.date.accessioned2013-02-13T09:37:31Z
dc.date.available2013-02-13T09:37:31Z
dc.date.issued2008-07-14
dc.identifierFOR ACCESS / DOWNLOAD PROBLEM -- PLEASE CONTACT LIBRARIAN, BOSE INSTITUTE, akc@bic.boseinst.ernet.inen_US
dc.identifier.citationBiswas S, Guharoy M and Chakrabarti P (2008) Structural segments and residue propensities in proteinRNA interfaces: comparison with protein-protein and protein-DNA complexes. Bioin/ormation 2(10), . 422-427.en_US
dc.identifier.issn0973-2063
dc.identifier.uri1. Full Text Link ->en_US
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC2561160/pdf/97320630002422.pdfen_US
dc.identifier.uri=================================================en_US
dc.identifier.uri2. Scopus : Citation Link ->en_US
dc.identifier.uri=================================================en_US
dc.description.abstractThe interface of a protein molecule that is involved in binding another protein, DNA or RNA has been characterized in terms of the number of unique secondary structural segments (SSSs), made up of stretches of helix, strand and non-regular (NR) regions. On average 10-11 segments define the protein interface in protein-protein (PP) and protein-DNA (PD) complexes, while the number is higher (14) for protein-RNA (PR) complexes. While the length of helical segments in PP interaction increases with the interface area, this is not the case in PD and PR complexes. The propensities of residues to occur in the three types of secondary structural elements (SSEs) in the interface relative to the corresponding elements in the protein tertiary structures have been calculated. Arg, Lys, Asn, Tyr, His and Gln are preferred residues in PR complexes; in addition, Ser and Thr are also favoured in PD interfaces.en_US
dc.language.isoenen_US
dc.publisherBiomedical Informaticsen_US
dc.subjectprotein-protein interactionsen_US
dc.subjectprotein-DNA interactionsen_US
dc.subjectprotein-RNA interactionsen_US
dc.subjectbinding interfaceen_US
dc.subjectprotein secondary structureen_US
dc.titleStructural segments and residue propensities in protein-RNA interfaces: comparison with protein-protein and protein-DNA complexesen_US
dc.title.alternativeBioinformationen_US
dc.typeArticleen_US


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